September 1, 2013

13 min read

The Truth about Genetically Modified Food

Proponents of genetically modified crops say the technology is the only way to feed a warming, increasingly populous world. Critics say we tamper with nature at our peril. Who is right?

By David H. Freedman

Robert Goldberg sags into his desk chair and gestures at the air. “Frankenstein monsters, things crawling out of the lab,” he says. “This the most depressing thing I've ever dealt with.”

Goldberg, a plant molecular biologist at the University of California, Los Angeles, is not battling psychosis. He is expressing despair at the relentless need to confront what he sees as bogus fears over the health risks of genetically modified (GM) crops. Particularly frustrating to him, he says, is that this debate should have ended decades ago, when researchers produced a stream of exonerating evidence: “Today we're facing the same objections we faced 40 years ago.”

Across campus, David Williams, a cellular biologist who specializes in vision, has the opposite complaint. “A lot of naive science has been involved in pushing this technology,” he says. “Thirty years ago we didn't know that when you throw any gene into a different genome, the genome reacts to it. But now anyone in this field knows the genome is not a static environment. Inserted genes can be transformed by several different means, and it can happen generations later.” The result, he insists, could very well be potentially toxic plants slipping through testing.

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Williams concedes that he is among a tiny minority of biologists raising sharp questions about the safety of GM crops. But he says this is only because the field of plant molecular biology is protecting its interests. Funding, much of it from the companies that sell GM seeds, heavily favors researchers who are exploring ways to further the use of genetic modification in agriculture. He says that biologists who point out health or other risks associated with GM crops—who merely report or defend experimental findings that imply there may be risks—find themselves the focus of vicious attacks on their credibility, which leads scientists who see problems with GM foods to keep quiet.

Whether Williams is right or wrong, one thing is undeniable: despite overwhelming evidence that GM crops are safe to eat, the debate over their use continues to rage, and in some parts of the world, it is growing ever louder. Skeptics would argue that this contentiousness is a good thing—that we cannot be too cautious when tinkering with the genetic basis of the world's food supply. To researchers such as Goldberg, however, the persistence of fears about GM foods is nothing short of exasperating. “In spite of hundreds of millions of genetic experiments involving every type of organism on earth,” he says, “and people eating billions of meals without a problem, we've gone back to being ignorant.”

So who is right: advocates of GM or critics? When we look carefully at the evidence for both sides and weigh the risks and benefits, we find a surprisingly clear path out of this dilemma.

Benefits and worries

The bulk of the science on GM safety points in one direction. Take it from David Zilberman, a U.C. Berkeley agricultural and environmental economist and one of the few researchers considered credible by both agricultural chemical companies and their critics. He argues that the benefits of GM crops greatly outweigh the health risks, which so far remain theoretical. The use of GM crops “has lowered the price of food,” Zilberman says. “It has increased farmer safety by allowing them to use less pesticide. It has raised the output of corn, cotton and soy by 20 to 30 percent, allowing some people to survive who would not have without it. If it were more widely adopted around the world, the price [of food] would go lower, and fewer people would die of hunger.”

In the future, Zilberman says, those advantages will become all the more significant. The United Nations Food and Agriculture Organization estimates that the world will have to grow 70 percent more food by 2050 just to keep up with population growth. Climate change will make much of the world's arable land more difficult to farm. GM crops, Zilberman says, could produce higher yields, grow in dry and salty land, withstand high and low temperatures, and tolerate insects, disease and herbicides.

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Credit: Jen Christiansen

Despite such promise, much of the world has been busy banning, restricting and otherwise shunning GM foods. Nearly all the corn and soybeans grown in the U.S. are genetically modified, but only two GM crops, Monsanto's MON810 maize and BASF's Amflora potato, are accepted in the European Union. Ten E.U. nations have banned MON810, and although BASF withdrew Amflora from the market in 2012, four E.U. nations have taken the trouble to ban that, too. Approval of a few new GM corn strains has been proposed there, but so far it has been repeatedly and soundly voted down. Throughout Asia, including in India and China, governments have yet to approve most GM crops, including an insect-resistant rice that produces higher yields with less pesticide. In Africa, where millions go hungry, several nations have refused to import GM foods in spite of their lower costs (the result of higher yields and a reduced need for water and pesticides). Kenya has banned them altogether amid widespread malnutrition. No country has definite plans to grow Golden Rice, a crop engineered to deliver more vitamin A than spinach (rice normally has no vitamin A), even though vitamin A deficiency causes more than one million deaths annually and half a million cases of irreversible blindness in the developing world.

Globally, only a tenth of the world's cropland includes GM plants. Four countries—the U.S., Canada, Brazil and Argentina—grow 90 percent of the planet's GM crops. Other Latin American countries are pushing away from the plants. And even in the U.S., voices decrying genetically modified foods are becoming louder. In 2016 the U.S. federal government passed a law requiring labeling of GM ingredients in food products, replacing GM-labeling laws in force or proposed in several dozen states.

The fear fueling all this activity has a long history. The public has been worried about the safety of GM foods since scientists at the University of Washington developed the first genetically modified tobacco plants in the 1970s. In the mid-1990s, when the first GM crops reached the market, Greenpeace, the Sierra Club, Ralph Nader, Prince Charles and a number of celebrity chefs took highly visible stands against them. Consumers in Europe became particularly alarmed: a survey conducted in 1997, for example, found that 69 percent of the Austrian public saw serious risks in GM foods, compared with only 14 percent of Americans.

In Europe, skepticism about GM foods has long been bundled with other concerns, such as a resentment of American agribusiness. Whatever it is based on, however, the European attitude reverberates across the world, influencing policy in countries where GM crops could have tremendous benefits. “In Africa, they don't care what us savages in America are doing,” Zilberman says. “They look to Europe and see countries there rejecting GM, so they don't use it.” Forces fighting genetic modification in Europe have rallied support for “the precautionary principle,” which holds that given the kind of catastrophe that would emerge from loosing a toxic, invasive GM crop on the world, GM efforts should be shut down until the technology is proved absolutely safe.

But as medical researchers know, nothing can really be “proved safe.” One can only fail to turn up significant risk after trying hard to find it—as is the case with GM crops.

A clean record

The human race has been selectively breeding crops, thus altering plants' genomes, for millennia. Ordinary wheat has long been strictly a human-engineered plant; it could not exist outside of farms, because its seeds do not scatter. For some 60 years scientists have been using “mutagenic” techniques to scramble the DNA of plants with radiation and chemicals, creating strains of wheat, rice, peanuts and pears that have become agricultural mainstays. The practice has inspired little objection from scientists or the public and has caused no known health problems.

The difference is that selective breeding or mutagenic techniques tend to result in large swaths of genes being swapped or altered. GM technology, in contrast, enables scientists to insert into a plant's genome a single gene (or a few of them) from another species of plant or even from a bacterium, virus or animal. Supporters argue that this precision makes the technology much less likely to produce surprises. Most plant molecular biologists also say that in the highly unlikely case that an unexpected health threat emerged from a new GM plant, scientists would quickly identify and eliminate it. “We know where the gene goes and can measure the activity of every single gene around it,” Goldberg says. “We can show exactly which changes occur and which don't.”

And although it might seem creepy to add virus DNA to a plant, doing so is, in fact, no big deal, proponents say. Viruses have been inserting their DNA into the genomes of crops, as well as humans and all other organisms, for millions of years. They often deliver the genes of other species while they are at it, which is why our own genome is loaded with genetic sequences that originated in viruses and nonhuman species. “When GM critics say that genes don't cross the species barrier in nature, that's just simple ignorance,” says Alan McHughen, a plant molecular geneticist at U.C. Riverside. Pea aphids contain fungi genes. Triticale is a century-plus-old hybrid of wheat and rye found in some flours and breakfast cereals. Wheat itself, for that matter, is a cross-species hybrid. “Mother Nature does it all the time, and so do conventional plant breeders,” McHughen says.

Could eating plants with altered genes allow new DNA to work its way into our own? It is possible but hugely improbable. Scientists have never found genetic material that could survive a trip through the human gut and make it into cells. Besides, we are routinely exposed to—and even consume—the viruses and bacteria whose genes end up in GM foods. The bacterium Bacillus thuringiensis , for example, which produces proteins fatal to insects, is sometimes enlisted as a natural pesticide in organic farming. “We've been eating this stuff for thousands of years,” Goldberg says.

In any case, proponents say, people have consumed as many as trillions of meals containing genetically modified ingredients over the past few decades. Not a single verified case of illness has ever been attributed to the genetic alterations. Mark Lynas, a prominent anti-GM activist who in 2013 publicly switched to strongly supporting the technology, has pointed out that every single news-making food disaster on record has been attributed to non-GM crops, such as the Escherichia coli –infected organic bean sprouts that killed 53 people in Europe in 2011.

Critics often disparage U.S. research on the safety of genetically modified foods, which is often funded or even conducted by GM companies, such as Monsanto. But much research on the subject comes from the European Commission, the administrative body of the E.U., which cannot be so easily dismissed as an industry tool. The European Commission has funded 130 research projects, carried out by more than 500 independent teams, on the safety of GM crops. None of those studies found any special risks from GM crops.

Plenty of other credible groups have arrived at the same conclusion. Gregory Jaffe, director of biotechnology at the Center for Science in the Public Interest, a science-based consumer-watchdog group in Washington, D.C., takes pains to note that the center has no official stance, pro or con, with regard to genetically modifying food plants. Yet Jaffe insists the scientific record is clear. “Current GM crops are safe to eat and can be grown safely in the environment,” he says. The American Association for the Advancement of Science, the American Medical Association and the National Academy of Sciences have all unreservedly backed GM crops. The U.S. Food and Drug Administration, along with its counterparts in several other countries, has repeatedly reviewed large bodies of research and concluded that GM crops pose no unique health threats. Dozens of review studies carried out by academic researchers have backed that view.

Opponents of genetically modified foods point to a handful of studies indicating possible safety problems. But reviewers have dismantled almost all of those reports. For example, a 1998 study by plant biochemist Árpád Pusztai, then at the Rowett Institute in Scotland, found that rats fed a GM potato suffered from stunted growth and immune system–related changes. But the potato was not intended for human consumption—it was, in fact, designed to be toxic for research purposes. The Rowett Institute later deemed the experiment so sloppy that it refuted the findings and charged Pusztai with misconduct.

Similar stories abound. Most recently, a team led by Gilles-Éric Séralini, a researcher at the University of Caen Lower Normandy in France, found that rats eating a common type of GM corn contracted cancer at an alarmingly high rate. But Séralini has long been an anti-GM campaigner, and critics charged that in his study, he relied on a strain of rat that too easily develops tumors, did not use enough rats, did not include proper control groups and failed to report many details of the experiment, including how the analysis was performed. After a review, the European Food Safety Authority dismissed the study's findings. Several other European agencies came to the same conclusion. “If GM corn were that toxic, someone would have noticed by now,” McHughen says. “Séralini has been refuted by everyone who has cared to comment.”

Some scientists say the objections to GM food stem from politics rather than science—that they are motivated by an objection to large multinational corporations having enormous influence over the food supply; invoking risks from genetic modification just provides a convenient way of whipping up the masses against industrial agriculture. “This has nothing to do with science,” Goldberg says. “It's about ideology.” Former anti-GM activist Lynas agrees. He has gone as far as labeling the anti-GM crowd “explicitly an antiscience movement.”

Persistent doubts

Not all objections to genetically modified foods are so easily dismissed, however. Long-term health effects can be subtle and nearly impossible to link to specific changes in the environment. Scientists have long believed that Alzheimer's disease and many cancers have environmental components, but few would argue we have identified all of them.

And opponents say that it is not true that the GM process is less likely to cause problems simply because fewer, more clearly identified genes are replaced. David Schubert, an Alzheimer's researcher who heads the Cellular Neurobiology Laboratory at the Salk Institute for Biological Studies in La Jolla, Calif., asserts that a single, well-characterized gene can still settle in the target plant's genome in many different ways. “It can go in forward, backward, at different locations, in multiple copies, and they all do different things,” he says. And as U.C.L.A.'s Williams notes, a genome often continues to change in the successive generations after the insertion, leaving it with a different arrangement than the one intended and initially tested. There is also the phenomenon of “insertional mutagenesis,” Williams adds, in which the insertion of a gene ends up quieting the activity of nearby genes.

True, the number of genes affected in a GM plant most likely will be far, far smaller than in conventional breeding techniques. Yet opponents maintain that because the wholesale swapping or alteration of entire packages of genes is a natural process that has been happening in plants for half a billion years, it tends to produce few scary surprises today. Changing a single gene, on the other hand, might turn out to be a more subversive action, with unexpected ripple effects, including the production of new proteins that might be toxins or allergens.

Opponents also point out that the kinds of alterations caused by the insertion of genes from other species might be more impactful, more complex or more subtle than those caused by the intraspecies gene swapping of conventional breeding. And just because there is no evidence to date that genetic material from an altered crop can make it into the genome of people who eat it does not mean such a transfer will never happen—or that it has not already happened and we have yet to spot it. These changes might be difficult to catch; their impact on the production of proteins might not even turn up in testing. “You'd certainly find out if the result is that the plant doesn't grow very well,” Williams says. “But will you find the change if it results in the production of proteins with long-term effects on the health of the people eating it?”

It is also true that many pro-GM scientists in the field are unduly harsh—even unscientific—in their treatment of critics. GM proponents sometimes lump every scientist who raises safety questions together with activists and discredited researchers. And even Séralini, the scientist behind the study that found high cancer rates for GM-fed rats, has his defenders. Most of them are nonscientists, or retired researchers from obscure institutions, or nonbiologist scientists, but the Salk Institute's Schubert also insists the study was unfairly dismissed. He says that as someone who runs drug-safety studies, he is well versed on what constitutes a good-quality animal toxicology study and that Séralini's makes the grade. He insists that the breed of rat in the study is commonly used in respected drug studies, typically in numbers no greater than in Séralini's study; that the methodology was standard; and that the details of the data analysis are irrelevant because the results were so striking.

Schubert joins Williams as one of a handful of biologists from respected institutions who are willing to sharply challenge the GM-foods-are-safe majority. Both charge that more scientists would speak up against genetic modification if doing so did not invariably lead to being excoriated in journals and the media. These attacks, they argue, are motivated by the fear that airing doubts could lead to less funding for the field. Says Williams: “Whether it's conscious or not, it's in their interest to promote this field, and they're not objective.”

Both scientists say that after publishing comments in respected journals questioning the safety of GM foods, they became the victims of coordinated attacks on their reputations. Schubert even charges that researchers who turn up results that might raise safety questions avoid publishing their findings out of fear of repercussions. “If it doesn't come out the right way,” he says, “you're going to get trashed.”

There is evidence to support that charge. In 2009 Nature detailed the backlash to a reasonably solid study published in the Proceedings of the National Academy of Sciences USA by researchers from Loyola University Chicago and the University of Notre Dame. The paper showed that GM corn seemed to be finding its way from farms into nearby streams and that it might pose a risk to some insects there because, according to the researchers' lab studies, caddis flies appeared to suffer on diets of pollen from GM corn. Many scientists immediately attacked the study, some of them suggesting the researchers were sloppy to the point of misconduct.

A way forward

There is a middle ground in this debate. Many moderate voices call for continuing the distribution of GM foods while maintaining or even stepping up safety testing on new GM crops. They advocate keeping a close eye on the health and environmental impact of existing ones. But they do not single out GM crops for special scrutiny, the Center for Science in the Public Interest's Jaffe notes: all crops could use more testing. “We should be doing a better job with food oversight altogether,” he says.

Even Schubert agrees. In spite of his concerns, he believes future GM crops can be introduced safely if testing is improved. “Ninety percent of the scientists I talk to assume that new GM plants are safety-tested the same way new drugs are by the FDA,” he says. “They absolutely aren't, and they absolutely should be.”

Stepped-up testing would pose a burden for GM researchers, and it could slow down the introduction of new crops. “Even under the current testing standards for GM crops, most conventionally bred crops wouldn't have made it to market,” McHughen says. “What's going to happen if we become even more strict?”

That is a fair question. But with governments and consumers increasingly coming down against GM crops altogether, additional testing may be the compromise that enables the human race to benefit from those crops' significant advantages.

David H. Freedman is a journalist who has been covering science, business and technology for more than 30 years.

Scientific American Magazine Vol 309 Issue 3

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Genetically modified foods: safety, risks and public concerns—a review

Defence Food Research Laboratory, Siddarthanagar, Mysore, 570011 India

K. R. Anilakumar

Genetic modification is a special set of gene technology that alters the genetic machinery of such living organisms as animals, plants or microorganisms. Combining genes from different organisms is known as recombinant DNA technology and the resulting organism is said to be ‘Genetically modified (GM)’, ‘Genetically engineered’ or ‘Transgenic’. The principal transgenic crops grown commercially in field are herbicide and insecticide resistant soybeans, corn, cotton and canola. Other crops grown commercially and/or field-tested are sweet potato resistant to a virus that could destroy most of the African harvest, rice with increased iron and vitamins that may alleviate chronic malnutrition in Asian countries and a variety of plants that are able to survive weather extremes. There are bananas that produce human vaccines against infectious diseases such as hepatitis B, fish that mature more quickly, fruit and nut trees that yield years earlier and plants that produce new plastics with unique properties. Technologies for genetically modifying foods offer dramatic promise for meeting some areas of greatest challenge for the 21st century. Like all new technologies, they also pose some risks, both known and unknown. Controversies and public concern surrounding GM foods and crops commonly focus on human and environmental safety, labelling and consumer choice, intellectual property rights, ethics, food security, poverty reduction and environmental conservation. With this new technology on gene manipulation what are the risks of “tampering with Mother Nature”?, what effects will this have on the environment?, what are the health concerns that consumers should be aware of? and is recombinant technology really beneficial? This review will also address some major concerns about the safety, environmental and ecological risks and health hazards involved with GM foods and recombinant technology.

Introduction

Scientists first discovered in 1946 that DNA can be transferred between organisms (Clive 2011 ). It is now known that there are several mechanisms for DNA transfer and that these occur in nature on a large scale, for example, it is a major mechanism for antibiotic resistance in pathogenic bacteria. The first genetically modified (GM) plant was produced in 1983, using an antibiotic-resistant tobacco plant. China was the first country to commercialize a transgenic crop in the early 1990s with the introduction of virus resistant tobacco. In 1994, the transgenic ‘Flavour Saver tomato’ was approved by the Food and Drug Administration (FDA) for marketing in the USA. The modification allowed the tomato to delay ripening after picking. In 1995, few transgenic crops received marketing approval. This include canola with modified oil composition (Calgene), Bacillus thuringiensis (Bt) corn/maize (Ciba-Geigy), cotton resistant to the herbicide bromoxynil (Calgene), Bt cotton (Monsanto), Bt potatoes (Monsanto), soybeans resistant to the herbicide glyphosate (Monsanto), virus-resistant squash (Asgrow) and additional delayed ripening tomatoes (DNAP, Zeneca/Peto, and Monsanto) (Clive 2011 ). A total of 35 approvals had been granted to commercially grow 8 transgenic crops and one flower crop of carnations with 8 different traits in 6 countries plus the EU till 1996 (Clive 1996 ). As of 2011, the USA leads a list of multiple countries in the production of GM crops. Currently, there are a number of food species in which a genetically modified version exists (Johnson 2008 ). Some of the foods that are available in the market include cotton, soybean, canola, potatoes, eggplant, strawberries, corn, tomatoes, lettuce, cantaloupe, carrots etc. GM products which are currently in the pipeline include medicines and vaccines, foods and food ingredients, feeds and fibres. Locating genes for important traits, such as those conferring insect resistance or desired nutrients-is one of the most limiting steps in the process.

Foods derived from GM crops

At present there are several GM crops used as food sources. As of now there are no GM animals approved for use as food, but a GM salmon has been proposed for FDA approval. In instances, the product is directly consumed as food, but in most of the cases, crops that have been genetically modified are sold as commodities, which are further processed into food ingredients.

Fruits and vegetables

Papaya has been developed by genetic engineering which is ring spot virus resistant and thus enhancing the productivity. This was very much in need as in the early 1990s the Hawaii’s papaya industry was facing disaster because of the deadly papaya ring spot virus. Its single-handed savior was a breed engineered to be resistant to the virus. Without it, the state’s papaya industry would have collapsed. Today 80 % of Hawaiian papaya is genetically engineered, and till now no conventional or organic method is available to control ring spot virus.

The NewLeaf™ potato, a GM food developed using naturally-occurring bacteria found in the soil known as Bacillus thuringiensis (Bt), was made to provide in-plant protection from the yield-robbing Colorado potato beetle. This was brought to market by Monsanto in the late 1990s, developed for the fast food market. This was forced to withdraw from the market in 2001as the fast food retailers did not pick it up and thereby the food processors ran into export problems. Reports say that currently no transgenic potatoes are marketed for the purpose of human consumption. However, BASF, one of the leading suppliers of plant biotechnology solutions for agriculture requested for the approval for cultivation and marketing as a food and feed for its ‘Fortuna potato’. This GM potato was made resistant to late blight by adding two resistance genes, blb1 and blb2, which was originated from the Mexican wild potato Solanum bulbocastanum . As of 2005, about 13 % of the zucchini grown in the USA is genetically modified to resist three viruses; the zucchini is also grown in Canada (Johnson 2008 ).

Vegetable oil

It is reported that there is no or a significantly small amount of protein or DNA remaining in vegetable oil extracted from the original GM crops in USA. Vegetable oil is sold to consumers as cooking oil, margarine and shortening, and is used in prepared foods. Vegetable oil is made of triglycerides extracted from plants or seeds and then refined, and may be further processed via hydrogenation to turn liquid oils into solids. The refining process removes nearly all non-triglyceride ingredients (Crevel et al. 2000 ). Cooking oil, margarine and shortening may also be made from several crops. A large percentage of Canola produced in USA is GM and is mainly used to produce vegetable oil. Canola oil is the third most widely consumed vegetable oil in the world. The genetic modifications are made for providing resistance to herbicides viz. glyphosate or glufosinate and also for improving the oil composition. After removing oil from canola seed, which is ∼43 %, the meal has been used as high quality animal feed. Canola oil is a key ingredient in many foods and is sold directly to consumers as margarine or cooking oil. The oil has many non-food uses, which includes making lipsticks.

Maize, also called corn in the USA and cornmeal, which is ground and dried maize constitute a staple food in many regions of the world. Grown since 1997 in the USA and Canada, 86 % of the USA maize crop was genetically modified in 2010 (Hamer and Scuse 2010 ) and 32 % of the worldwide maize crop was GM in 2011 (Clive 2011 ). A good amount of the total maize harvested go for livestock feed including the distillers grains. The remaining has been used for ethanol and high fructose corn syrup production, export, and also used for other sweeteners, cornstarch, alcohol, human food or drink. Corn oil is sold directly as cooking oil and to make shortening and margarine, in addition to make vitamin carriers, as a source of lecithin, as an ingredient in prepared foods like mayonnaise, sauces and soups, and also to fry potato chips and French fries. Cottonseed oil is used as a salad and cooking oil, both domestically and industrially. Nearly 93 % of the cotton crop in USA is GM.

The USA imports 10 % of its sugar from other countries, while the remaining 90 % is extracted from domestically grown sugar beet and sugarcane. Out of the domestically grown sugar crops, half of the extracted sugar is derived from sugar beet, and the other half is from sugarcane. After deregulation in 2005, glyphosate-resistant sugar beet was extensively adopted in the USA. In USA 95 % of sugar beet acres were planted with glyphosate-resistant seed (Clive 2011 ). Sugar beets that are herbicide-tolerant have been approved in Australia, Canada, Colombia, EU, Japan, Korea, Mexico, New Zealand, Philippines, Russian Federation, Singapore and USA. The food products of sugar beets are refined sugar and molasses. Pulp remaining from the refining process is used as animal feed. The sugar produced from GM sugar beets is highly refined and contains no DNA or protein—it is just sucrose, the same as sugar produced from non-GM sugar beets (Joana et al. 2010 ).

Quantification of genetically modified organisms (GMOs) in foods

Testing on GMOs in food and feed is routinely done using molecular techniques like DNA microarrays or qPCR. These tests are based on screening genetic elements like p35S, tNos, pat, or bar or event specific markers for the official GMOs like Mon810, Bt11, or GT73. The array based method combines multiplex PCR and array technology to screen samples for different potential GMO combining different approaches viz. screening elements, plant-specific markers, and event-specific markers. The qPCR is used to detect specific GMO events by usage of specific primers for screening elements or event specific markers. Controls are necessary to avoid false positive or false negative results. For example, a test for CaMV is used to avoid a false positive in the event of a virus contaminated sample.

Joana et al. ( 2010 ) reported the extraction and detection of DNA along with a complete industrial soybean oil processing chain to monitor the presence of Roundup Ready (RR) soybean. The amplification of soybean lectin gene by end-point polymerase chain reaction (PCR) was achieved in all the steps of extraction and refining processes. The amplification of RR soybean by PCR assays using event specific primers was also achieved for all the extraction and refining steps. This excluded the intermediate steps of refining viz. neutralization, washing and bleaching possibly due to sample instability. The real-time PCR assays using specific probes confirmed all the results and proved that it is possible to detect and quantify GMOs in the fully refined soybean oil.

Figure  1 gives the overall protocol for the testing of GMOs. This is based on a PCR detection system specific for 35S promoter region originating from cauliflower mosaic virus (Deisingh and Badrie 2005 ). The 35S-PCR technique permits detection of GMO contents of foods and raw materials in the range of 0.01–0.1 %. The development of quantitative detection systems such as quantitative competitive PCR (QC-PCR), real-time PCR and ELISA systems resulted in the advantage of survival of DNA in most manufacturing processes. Otherwise with ELISA, there can be protein denaturing during food processing. Inter-laboratory differences were found to be less with the QC-PCR than with quantitative PCR probably due to insufficient homogenisation of the sample. However, there are disadvantages, the major one being the amount of DNA, which could be amplified, is affected by food processing techniques and can vary up to 5-fold. Thus, results need to be normalised by using plant-specific QC-PCR system. Further, DNA, which cannot be amplified, will affect all quantitative PCR detection systems.

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Protocol for the testing of genetically modified foods

In a recent work La Mura et al. ( 2011 ) applied QUIZ (quantization using informative zeros) to estimate the contents of RoundUp Ready™ soya and MON810 in processed food containing one or both GMs. They reported that the quantification of GM in samples can be performed without the need for certified reference materials using QUIZ. Results showed good agreement between derived values and known input of GM material and compare favourably with quantitative real-time PCR. Detection of Roundup Ready soybean by loop-mediated isothermal amplification combined with a lateral-flow dipstick has been reported recently (Xiumin et al. 2012 ).

GM foods-merits and demerits

Before we think of having GM foods it is very important to know about is advantages and disadvantages especially with respect to its safety. These foods are made by inserting genes of other species into their DNA. Though this kind of genetic modification is used both in plants and animals, it is found more commonly in the former than in the latter. Experts are working on developing foods that have the ability to alleviate certain disorders and diseases. Though researchers and the manufacturers make sure that there are various advantages of consuming these foods, a fair bit of the population is entirely against them.

GM foods are useful in controlling the occurrence of certain diseases. By modifying the DNA system of these foods, the properties causing allergies are eliminated successfully. These foods grow faster than the foods that are grown traditionally. Probably because of this, the increased productivity provides the population with more food. Moreover these foods are a boon in places which experience frequent droughts, or where the soil is incompetent for agriculture. At times, genetically engineered food crops can be grown at places with unfavourable climatic conditions too. A normal crop can grow only in specific season or under some favourable climatic conditions. Though the seeds for such foods are quite expensive, their cost of production is reported to be less than that of the traditional crops due to the natural resistance towards pests and insects. This reduces the necessity of exposing GM crops to harmful pesticides and insecticides, making these foods free from chemicals and environment friendly as well. Genetically engineered foods are reported to be high in nutrients and contain more minerals and vitamins than those found in traditionally grown foods. Other than this, these foods are known to taste better. Another reason for people opting for genetically engineered foods is that they have an increased shelf life and hence there is less fear of foods getting spoiled quickly.

The biggest threat caused by GM foods is that they can have harmful effects on the human body. It is believed that consumption of these genetically engineered foods can cause the development of diseases which are immune to antibiotics. Besides, as these foods are new inventions, not much is known about their long term effects on human beings. As the health effects are unknown, many people prefer to stay away from these foods. Manufacturers do not mention on the label that foods are developed by genetic manipulation because they think that this would affect their business, which is not a good practice. Many religious and cultural communities are against such foods because they see it as an unnatural way of producing foods. Many people are also not comfortable with the idea of transferring animal genes into plants and vice versa. Also, this cross-pollination method can cause damage to other organisms that thrive in the environment. Experts are also of the opinion that with the increase of such foods, developing countries would start depending more on industrial countries because it is likely that the food production would be controlled by them in the time to come.

Safety tests on commercial GM crops

The GM tomatoes were produced by inserting kanr genes into a tomato by an ‘antisense’ GM method (IRDC 1998 ). The results show that there were no significant alterations in total protein, vitamins and mineral contents and in toxic glycoalkaloids (Redenbaugh et al. 1992 ). Therefore, the GM and parent tomatoes were deemed to be “substantially equivalent”. In acute toxicity studies with male/female rats, which were tube-fed with homogenized GM tomatoes, toxic effects were reported to be absent. A study with a GM tomato expressing B. thuringiensis toxin CRYIA (b) was underlined by the immunocytochemical demonstration of in vitro binding of Bt toxin to the caecum/colon from humans and rhesus monkeys (Noteborn et al. 1995 ).

Two lines of Chardon LL herbicide-resistant GM maize expressing the gene of phosphinothricin acetyltransferase before and after ensiling showed significant differences in fat and carbohydrate contents compared with non-GM maize and were therefore substantially different come. Toxicity tests were only performed with the maize even though with this the unpredictable effects of the gene transfer or the vector or gene insertion could not be demonstrated or excluded. The design of these experiments was also flawed because of poor digestibility and reduction in feed conversion efficiency of GM corn. One broiler chicken feeding study with rations containing transgenic Event 176 derived Bt corn (Novartis) has been published (Brake and Vlachos 1998 ). However, the results of this trial are more relevant to commercial than academic scientific studies.

GM soybeans

To make soybeans herbicide resistant, the gene of 5-enolpyruvylshikimate-3-phosphate synthase from Agrobacterium was used. Safety tests claim the GM variety to be “substantially equivalent” to conventional soybeans (Padgette et al. 1996 ). The same was claimed for GTS (glyphosate-resistant soybeans) sprayed with this herbicide (Taylor et al. 1999 ). However, several significant differences between the GM and control lines were recorded (Padgette et al. 1996 ) and the study showed statistically significant changes in the contents of genistein (isoflavone) with significant importance for health (Lappe et al. 1999 ) and increased content in trypsin inhibitor.

Studies have been conducted on the feeding value (Hammond et al. 1996 ) and possible toxicity (Harrison et al. 1996 ) for rats, broiler chickens, catfish and dairy cows of two GM lines of glyphosate-resistant soybean (GTS). The growth, feed conversion efficiency, catfish fillet composition, broiler breast muscle and fat pad weights and milk production, rumen fermentation and digestibilities in cows were found to be similar for GTS and non-GTS. These studies had the following lacunae: (a) No individual feed intakes, body or organ weights were given and histology studies were qualitative microscopy on the pancreas, (b) The feeding value of the two GTS lines was not substantially equivalent either because the rats/catfish grew significantly better on one of the GTS lines than on the other, (c) The design of study with broiler chicken was not much convincing, (d) Milk production and performance of lactating cows also showed significant differences between cows fed GM and non-GM feeds and (e) Testing of the safety of 5-enolpyruvylshikimate-3-phosphate synthase, which renders soybeans glyphosate-resistant (Harrison et al. 1996 ), was irrelevant because in the gavage studies an E. coli recombinant and not the GTS product were used. In a separate study (Teshima et al. 2000 ), it was claimed that rats and mice which were fed 30 % toasted GTS or non-GTS in their diet had no significant differences in nutritional performance, organ weights, histopathology and production of IgE and IgG antibodies.

GM potatoes

There were no improvements in the protein content or amino acid profile of GM potatoes (Hashimoto et al. 1999a ). In a short feeding study to establish the safety of GM potatoes expressing the soybean glycinin gene, rats were daily force-fed with 2 g of GM or control potatoes/kg body weight (Hashimoto et al 1999b ). No differences in growth, feed intake, blood cell count and composition and organ weights between the groups were found. In this study, the intake of potato by animals was reported to be too low (Pusztai 2001 ).

Feeding mice with potatoes transformed with a Bacillus thuringiensis var. kurstaki Cry1 toxin gene or the toxin itself was shown to have caused villus epithelial cell hypertrophy and multinucleation, disrupted microvilli, mitochondrial degeneration, increased numbers of lysosomes and autophagic vacuoles and activation of crypt Paneth cells (Fares and El-Sayed 1998 ). The results showed CryI toxin which was stable in the mouse gut. Growing rats pair-fed on iso -proteinic and iso -caloric balanced diets containing raw or boiled non-GM potatoes and GM potatoes with the snowdrop ( Galanthus nivalis ) bulb lectin (GNA) gene (Ewen and Pusztai 1999 ) showed significant increase in the mucosal thickness of the stomach and the crypt length of the intestines of rats fed GM potatoes. Most of these effects were due to the insertion of the construct used for the transformation or the genetic transformation itself and not to GNA which had been pre-selected as a non-mitotic lectin unable to induce hyperplastic intestinal growth (Pusztai et al. 1990 ) and epithelial T lymphocyte infiltration.

The kind that expresses soybean glycinin gene (40–50 mg glycinin/g protein) was developed (Momma et al. 1999 ) and was claimed to contain 20 % more protein. However, the increased protein content was found probably due to a decrease in moisture rather than true increase in protein.

Several lines of GM cotton plants have been developed using a gene from Bacillus thuringiensis subsp. kurstaki providing increased protection against major lepidopteran pests. The lines were claimed to be “substantially equivalent” to parent lines (Berberich et al. 1996 ) in levels of macronutrients and gossypol. Cyclopropenoid fatty acids and aflatoxin levels were less than those in conventional seeds. However, because of the use of inappropriate statistics it was questionable whether the GM and non-GM lines were equivalent, particularly as environmental stresses could have unpredictable effects on anti-nutrient/toxin levels (Novak and Haslberger 2000 ).

The nutritional value of diets containing GM peas expressing bean alpha-amylase inhibitor when fed to rats for 10 days at two different doses viz. 30 % and 65 % was shown to be similar to that of parent-line peas (Pusztai et al. 1999 ). At the same time in order to establish its safety for humans a more rigorous specific risk assessment will have to be carried out with several GM lines. Nutritional/toxicological testing on laboratory animals should follow the clinical, double-blind, placebo-type tests with human volunteers.

Allergenicity studies

When the gene is from a crop of known allergenicity, it is easy to establish whether the GM food is allergenic using in vitro tests, such as RAST or immunoblotting, with sera from individuals sensitised to the original crop. This was demonstrated in GM soybeans expressing the brasil nut 2S proteins (Nordlee et al. 1996 ) or in GM potatoes expressing cod protein genes (Noteborn et al. 1995 ). It is also relatively easy to assess whether genetic engineering affected the potency of endogenous allergens (Burks and Fuchs 1995 ). Farm workers exposed to B. thuringiensis pesticide were shown to have developed skin sensitization and IgE antibodies to the Bt spore extract. With their sera it may now therefore be possible to test for the allergenic potential of GM crops expressing Bt toxin (Bernstein et al. 1999 ). It is all the more important because Bt toxin Cry1Ac has been shown to be a potent oral/nasal antigen and adjuvant (Vazquez-Padron et al. 2000 ).

The decision-tree type of indirect approach based on factors such as size and stability of the transgenically expressed protein (O’Neil et al. 1998 ) is even more unsound, particularly as its stability to gut proteolysis is assessed by an in vitro (simulated) testing (Metcalf et al. 1996 ) instead of in vivo (human/animal) testing and this is fundamentally wrong. The concept that most allergens are abundant proteins may be misleading because, for example, Gad c 1, the major allergen in codfish, is not a predominant protein (Vazquez-Padron et al. 2000 ). However, when the gene responsible for the allergenicity is known, such as the gene of the alpha-amylase/trypsin inhibitors/allergens in rice, cloning and sequencing opens the way for reducing their level by antisense RNA strategy (Nakamura and Matsuda 1996 ).

It is known that the main concerns about adverse effects of GM foods on health are the transfer of antibiotic resistance, toxicity and allergenicity. There are two issues from an allergic standpoint. These are the transfer of a known allergen that may occur from a crop into a non-allergenic target crop and the creation of a neo-allergen where de novo sensitisation occurs in the population. Patients allergic to Brazil nuts and not to soy bean then showed an IgE mediated response towards GM soy bean. Lack ( 2002 ) argued that it is possible to prevent such occurrences by doing IgE-binding studies and taking into account physico-chemical characteristics of proteins and referring to known allergen databases. The second possible scenario of de novo sensitisation does not easily lend itself to risk assessment. He reports that evidence that the technology used for the production of GM foods poses an allergic threat per se is lacking very much compared to other methodologies widely accepted in the food industry.

Risks and controversy

There are controversies around GM food on several levels, including whether food produced with it is safe, whether it should be labelled and if so how, whether agricultural biotechnology and it is needed to address world hunger now or in the future, and more specifically with respect to intellectual property and market dynamics, environmental effects of GM crops and GM crops’ role in industrial agricultural more generally.

Many problems, viz. the risks of “tampering with Mother Nature”, the health concerns that consumers should be aware of and the benefits of recombinant technology, also arise with pest-resistant and herbicide-resistant plants. The evolution of resistant pests and weeds termed superbugs and super weeds is another problem. Resistance can evolve whenever selective pressure is strong enough. If these cultivars are planted on a commercial scale, there will be strong selective pressure in that habitat, which could cause the evolution of resistant insects in a few years and nullify the effects of the transgenic. Likewise, if spraying of herbicides becomes more regular due to new cultivars, surrounding weeds could develop a resistance to the herbicide tolerant by the crop. This would cause an increase in herbicide dose or change in herbicide, as well as an increase in the amount and types of herbicides on crop plants. Ironically, chemical companies that sell weed killers are a driving force behind this research (Steinbrecher 1996 ).

Another issue is the uncertainty in whether the pest-resistant characteristic of these crops can escape to their weedy relatives causing resistant and increased weeds (Louda 1999 ). It is also possible that if insect-resistant plants cause increased death in one particular pest, it may decrease competition and invite minor pests to become a major problem. In addition, it could cause the pest population to shift to another plant population that was once unthreatened. These effects can branch out much further. A study of Bt crops showed that “beneficial insects, so named because they prey on crop pests, were also exposed to harmful quantities of Bt.” It was stated that it is possible for the effects to reach further up the food web to effect plants and animals consumed by humans (Brian 1999 ). Also, from a toxicological standpoint, further investigation is required to determine if residues from herbicide or pest resistant plants could harm key groups of organisms found in surrounding soil, such as bacteria, fungi, nematodes, and other microorganisms (Allison and Palma 1997 ).

The potential risks accompanied by disease resistant plants deal mostly with viral resistance. It is possible that viral resistance can lead to the formation of new viruses and therefore new diseases. It has been reported that naturally occurring viruses can recombine with viral fragments that are introduced to create transgenic plants, forming new viruses. Additionally, there can be many variations of this newly formed virus (Steinbrecher 1996 ).

Health risks associated with GM foods are concerned with toxins, allergens, or genetic hazards. The mechanisms of food hazards fall into three main categories (Conner and Jacobs 1999 ). They are inserted genes and their expression products, secondary and pleiotropic effects of gene expression and the insertional mutagenesis resulting from gene integration. With regards to the first category, it is not the transferred gene itself that would pose a health risk. It should be the expression of the gene and the affects of the gene product that are considered. New proteins can be synthesized that can produce unpredictable allergenic effects. For example, bean plants that were genetically modified to increase cysteine and methionine content were discarded after the discovery that the expressed protein of the transgene was highly allergenic (Butler and Reichhardt 1999 ). Due attention should be taken for foods engineered with genes from foods that commonly cause allergies, such as milk, eggs, nuts, wheat, legumes, fish, molluscs and crustacean (Maryanski 1997 ). However, since the products of the transgenic are usually previously identified, the amount and effects of the product can be assessed before public consumption. Also, any potential risk, immunological, allergenic, toxic or genetically hazardous, could be recognized and evaluated if health concerns arise. The available allergen data bases with details are shown in Table  1 .

Allergen databases (Kleter and Peijnenburg 2002 )

More concern comes with secondary and pleiotropic effects. For example, many transgenes encode an enzyme that alters biochemical pathways. This could cause an increase or decrease in certain biochemicals. Also, the presence of a new enzyme could cause depletion in the enzymatic substrate and subsequent build up of the enzymatic product. In addition, newly expressed enzymes may cause metabolites to diverge from one secondary metabolic pathway to another (Conner and Jacobs 1999 ). These changes in metabolism can lead to an increase in toxin concentrations. Assessing toxins is a more difficult task due to limitations of animal models. Animals have high variation between experimental groups and it is challenging to attain relevant doses of transgenic foods in animals that would provide results comparable to humans (Butler and Reichhardt 1999 ). Consequently, biochemical and regulatory pathways in plants are poorly understood.

Insertional mutagenesis can disrupt or change the expression of existing genes in a host plant. Random insertion can cause inactivation of endogenous genes, producing mutant plants. Moreover, fusion proteins can be made from plant DNA and inserted DNA. Many of these genes create nonsense products or are eliminated in crop selection due to incorrect appearance. However, of most concern is the activation or up regulation of silent or low expressed genes. This is due to the fact that it is possible to activate “genes that encode enzymes in biochemical pathways toward the production of toxic secondary compounds” (Conner and Jacobs 1999 ). This becomes a greater issue when the new protein or toxic compound is expressed in the edible portion of the plant, so that the food is no longer substantially equal to its traditional counterpart.

There is a great deal of unknowns when it comes to the risks of GM foods. One critic declared “foreign proteins that have never been in the human food chain will soon be consumed in large amounts”. It took us many years to realize that DDT might have oestrogenic activities and affect humans, “but we are now being asked to believe that everything is OK with GM foods because we haven’t seen any dead bodies yet” (Butler and Reichhardt 1999 ). As a result of the growing public concerns over GM foods, national governments have been working to regulate production and trade of GM foods.

Reports say that GM crops are grown over 160 million hectares in 29 countries, and imported by countries (including European ones) that don’t grow them. Nearly 300 million Americans, 1350 million Chinese, 280 million Brazilians and millions elsewhere regularly eat GM foods, directly and indirectly. Though Europeans voice major fears about GM foods, they permit GM maize cultivation. It imports GM soy meal and maize as animal feed. Millions of Europeans visit the US and South America and eat GM food.

Around three million Indians have become US citizens, and millions more go to the US for tourism and business and they will be eating GM foods in the USA. Indian activists claim that GM foods are inherently dangerous and must not be cultivated in India. Activists strongly opposed Bt cotton in India, and published reports claiming that the crop had failed in the field. At the same time farmers soon learned from experience that Bt cotton was very profitable, and 30 million rushed to adopt it. In consequence, India’s cotton production doubled and exports zoomed, even while using much less pesticide. Punjab farmers lease land at Rs 30,000 per acre to grow Bt cotton.

Public concerns-global scenario

In the late 1980s, there was a major controversy associated with GM foods even when the GMOs were not in the market. But the industrial applications of gene technology were developed to the production and marketing status. After words, the European Commission harmonized the national regulations across Europe. Concerns from the community side on GMOs in particular about its authorization have taken place since 1990s and the regulatory frame work on the marketing aspects underwent refining. Issues specifically on the use of GMOs for human consumption were introduced in 1997, in the Regulation on Novel Foods Ingredients (258/97/EC of 27 January 1997). This Regulations deals with rules for authorization and labelling of novel foods including food products made from GMOs, recognizing for the first time the consumer’s right to information and labelling as a tool for making an informed choice. The labelling of GM maize varieties and GM soy varieties that did not fall under this Regulation are covered by Regulation (EC 1139/98). Further legislative initiatives concern the traceability and labelling of GMOs and the authorization of GMOs in food and feed.

The initial outcome of the implementation of the first European directive seemed to be a settlement of the conflicts over technologies related to gene applications. By 1996, the second international level controversy over gene technology came up and triggered the arrival of GM soybeans at European harbours (Lassen et al. 2002 ). The GM soy beans by Monsanto to resist the herbicide represented the first large scale marketing of GM foods in Europe. Events such as commercialisation of GM maize and other GM modified commodities focused the public attention on the emerging biosciences, as did other gene technology applications such as animal and human cloning. The public debate on the issues associated with the GM foods resulted in the formation of many non-governmental organizations with explicit interest. At the same time there is a great demand for public participation in the issues about regulation and scientific strategy who expresses acceptance or rejection of GM products through purchase decisions or consumer boycotts (Frewer and Salter 2002 ).

Most research effort has been devoted to assessing people’s attitudes towards GM foods as a technology. Numerous “opinion poll”—type surveys have been conducted on national and cross-national levels (Hamstra 1998 ). Ethical concerns are also important, that a particular technology is in some way “tampering with nature”, or that unintended effects are unpredictable and thus unknown to science (Miles and Frewer 2001 ).

Consumer’s attitude towards GM foods

Consumer acceptance is conditioned by the risk that they perceive from introducing food into their consumption habits processed through technology that they hardly understand. In a study conducted in Spain, the main conclusion was that the introduction of GM food into agro-food markets should be accompanied by adequate policies to guarantee consumer safety. These actions would allow a decrease in consumer-perceived risk by taking special care of the information provided, concretely relating to health. For, the most influential factor in consumer-perceived risk from these foods is concern about health (Martinez-Poveda et al. 2009 ).

Tsourgiannis et al. ( 2011 ) conducted a study aimed to identify the factors that affect consumers purchasing behaviour towards food products that are free from GMO (GM Free) in a European region and more precisely in the Prefecture of Drama-Kavala-Xanthi. Field interviews conducted in a random selected sample consisted of 337 consumers in the cities of Drama, Kavala, Xanthi in 2009. Principal components analysis (PCA) was conducted in order to identify the factors that affect people in preferring consuming products that are GM Free. The factors that influence people in the study area to buy GM Free products are: (a) products’ certification as GM Free or organic products, (b) interest about the protection of the environment and nutrition value, (c) marketing issues and (d) price and quality. Furthermore, cluster and discriminant analysis identified two groups of consumers: (a) those influenced by the product price, quality and marketing aspects and (b) those interested in product’s certification and environmental protection (Tsourgiannis et al. 2011 ).

Snell et al. ( 2012 ) examined 12 long-term studies (of more than 90 days, up to 2 years in duration) and 12 multigenerational studies (from 2 to 5 generations) on the effects of diets containing GM maize, potato, soybean, rice, or triticale on animal health. They referenced the 90-day studies on GM feed for which long-term or multigenerational study data were available. Many parameters have been examined using biochemical analyses, histological examination of specific organs, hematology and the detection of transgenic DNA. Results from all the 24 studies do not suggest any health hazards and, in general, there were no statistically significant differences within parameters observed. They observed some small differences, though these fell within the normal variation range of the considered parameter and thus had no biological or toxicological significance. The studies reviewed present evidence to show that GM plants are nutritionally equivalent to their non-GM counterparts and can be safely used in food and feed.

GM foods: issues with respect to India

In a major setback to the proponents of GM technology in farm crops, the Parliamentary Committee on Agriculture in 2012 asked Indian government to stop all field trials and sought a bar on GM food crops such as Bt. brinjal. Raising the “ethical dimensions” of transgenics in agricultural crops, as well as studies of a long-term environmental and chronic toxicology impact, the panel noted that there were no significant socio-economic benefits to farmers.

Countries like India have great security concerns at the same time specific problems exist for small and marginal farmers. India could use a toxin free variety of the Lathyrus sativus grown on marginal lands and consumed by the very poor. GM mustard is a variety using the barnase-barstar-bar gene complex, an unstable gene construct with possible undesirable effects, to achieve male sterile lines that are used to make hybrid mustard varieties. In India we have good non-GM alternatives for making male sterile lines for hybrid production so the Proagro variety is of little use. Being a food crop, GM mustard will have to be examined very carefully. Even if there were to be benefits, they have to be weighed against the risks posed to human health and the environment. Apart from this, mustard is a cross-pollinating crop and pollen with their foreign genes is bound to reach non-GM mustard and wild relatives. We do not know what impact this will have. If GM technology is to be used in India, it should be directed at the real needs of Indian farmers, on crops like legumes, oilseeds and fodder and traits like drought tolerance and salinity tolerance.

Basmati rice and Darjeeling tea are perhaps India’s most easily identifiable premium products in the area of food. Basmati is highly prized rice, its markets are growing and it is a high end, expensive product in the international market. Like Champagne wine and truffles from France, international consumers treat it as a special, luxury food. Since rice is nutritionally a poor cereal, it is thought that addition of iron and vitamin A by genetic modification would increase the nutritional quality. So does it make any sense at all to breed a GM Basmati, along the lines of Bt Cotton? However, premium wine makers have outright rejected the notion of GM doctored wines that were designed to cut out the hangover and were supposed to be ‘healthier’. Premium products like special wines, truffles and Basmati rice need to be handled in a special, premium way (Sahai 2003 ).

Traceability of GMOs in the food production chain

Traceability systems document the history of a product and may serve the purpose of both marketing and health protection. In this framework, segregation and identity preservation systems allow for the separation of GM and non-GM products from “farm to fork”. Implementation of these systems comes with specific technical requirements for each particular step of the food processing chain. In addition, the feasibility of traceability systems depends on a number of factors, including unique identifiers for each GM product, detection methods, permissible levels of contamination, and financial costs. Progress has been achieved in the field of sampling, detection, and traceability of GM products, while some issues remain to be solved. For success, much will depend on the threshold level for adventitious contamination set by legislation (Miraglia et al. 2004 ).

Issues related to detection and traceability of GMOs is gaining interest worldwide due to the global diffusion and the related socio-economical implications. The interest of the scientific community into traceability aspects has also been increased simultaneously. Crucial factors in sampling and detection methodologies are the number of the GMOs involved and international agreement on traceability. The availability of reliable traceability strategies is very important and this may increase public trust in transparency in GMO related issues.

Heat processing methods like autoclaving and microwave heating can damage the DNA and reduce the level to detectable DNA. The PCR based methods have been standardised to detect such DNA in GM soybean and maize (Vijayakumar et al. 2009 ). Molecular methods such as multiplex and real time PCR methods have been developed to detect even 20 pg of genomic DNA in genetically modified EE-1 brinjal (Ballari et al. 2012 ).

DNA and protein based methods have been adopted for the detection and identification of GMOs which is relatively a new area of diagnostics. New diagnostic methodologies are also being developed, viz. the microarray-based methods that allow for the simultaneous identification of the increasing number of GMOs on the global market in a single sample. Some of these techniques have also been discussed for the detection of unintended effects of genetic modification by Cellini et al. ( 2004 ). The implementation of adequate traceability systems requires more than technical tools alone and is strictly linked to labelling constraints. The more stringent the labelling requirements, the more expensive and difficult the associated traceability strategies are to meet these requirements.

Both labelling and traceability of GMOs are current issues that are considered in trade and regulation. Currently, labelling of GM foods containing detectable transgenic material is required by EU legislation. A proposed package of legislation would extend this labelling to foods without any traces of transgenics. These new legislations would also impose labelling and a traceability system based on documentation throughout the food and feed manufacture system. The regulatory issues of risk analysis and labelling are currently harmonised by Codex Alimentarius. The implementation and maintenance of the regulations necessitates sampling protocols and analytical methodologies that allow for accurate determination of the content of GM organisms within a food and feed sample. Current methodologies for the analysis of GMOs are focused on either one of two targets, the transgenic DNA inserted- or the novel protein(s) expressed- in a GM product. For most DNA-based detection methods, the polymerase chain reaction is employed. Items that need consideration in the use of DNA-based detection methods include the specificity, sensitivity, matrix effects, internal reference DNA, availability of external reference materials, hemizygosity versus homozygosity, extra chromosomal DNA and international harmonisation.

For most protein-based methods, enzyme-linked immunosorbent assays with antibodies binding the novel protein are employed. Consideration should be given to the selection of the antigen bound by the antibody, accuracy, validation and matrix effects. Currently, validation of detection methods for analysis of GMOs is taking place. New methodologies are developed, in addition to the use of microarrays, mass spectrometry and surface plasmon resonance. Challenges for GMO detection include the detection of transgenic material in materials with varying chromosome numbers. The existing and proposed regulatory EU requirements for traceability of GM products fit within a broader tendency towards traceability of foods in general and, commercially, towards products that can be distinguished from one another.

Gene transfer studies in human volunteers

As of January 2009, there has only been one human feeding study conducted on the effects of GM foods. The study involved seven human volunteers who previously had their large intestines removed for medical reasons. These volunteers were provided with GM soy to eat to see if the DNA of the GM soy transferred to the bacteria that naturally lives in the human gut. Researchers identified that three of the seven volunteers had transgenes from GM soya transferred into the bacteria living in their gut before the start of the feeding experiment. As this low-frequency transfer did not increase after the consumption of GM soy, the researchers concluded that gene transfer did not occur during the experiment. In volunteers with complete digestive tracts, the transgene did not survive passage through intact gastrointestinal tract (Netherwood 2004 ). Other studies have found DNA from M13 virus, GFP and even ribulose-1, 5-bisphosphate carboxylase (Rubisco) genes in the blood and tissue of ingesting animals (Guertler et al. 2009 ; Brigulla and Wackernagel 2010 ).

Two studies on the possible effects of giving GM feed to animals found that there were no significant differences in the safety and nutritional value of feedstuffs containing material derived from GM plants (Gerhard et al. 2005 ; Beagle et al. 2006 ). Specifically, the studies noted that no residues of recombinant DNA or novel proteins have been found in any organ or tissue samples obtained from animals fed with GM plants (Nordlee 1996 ; Streit 2001 ).

Future developments

The GM foods have the potential to solve many of the world’s hunger and malnutrition problems, and to help protect and preserve the environment by increasing yield and reducing reliance upon synthetic pesticides and herbicides. Challenges ahead lie in many areas viz. safety testing, regulation, policies and food labelling. Many people feel that genetic engineering is the inevitable wave of the future and that we cannot afford to ignore a technology that has such enormous potential benefits.

Future also envisages that applications of GMOs are diverse and include drugs in food, bananas that produce human vaccines against infectious diseases such as Hepatitis B (Kumar et al. 2005 ), metabolically engineered fish that mature more quickly, fruit and nut trees that yield years earlier, foods no longer containing properties associated with common intolerances, and plants that produce new biodegradable plastics with unique properties (van Beilen and Yves 2008 ). While their practicality or efficacy in commercial production has yet to be fully tested, the next decade may see exponential increases in GM product development as researchers gain increasing access to genomic resources that are applicable to organisms beyond the scope of individual projects.

One has to agree that there are many opinions (Domingo 2000 ) about scarce data on the potential health risks of GM food crops, even though these should have been tested for and eliminated before their introduction. Although it is argued that small differences between GM and non-GM crops have little biological meaning, it is opined that most GM and parental line crops fall short of the definition of substantial equivalence. In any case, we need novel methods and concepts to probe into the compositional, nutritional, toxicological and metabolic differences between GM and conventional crops and into the safety of the genetic techniques used in developing GM crops if we want to put this technology on a proper scientific foundation and allay the fears of the general public. Considerable effort need to be directed towards understanding people’s attitudes towards this gene technology. At the same time it is imperative to note the lack of trust in institutions and institutional activities regarding GMOs and the public perceive that institutions have failed to take account of the actual concerns of the public as part of their risk management activities.

Contributor Information

A. S. Bawa, Email: ni.oc.oohay@awabrednirama .

K. R. Anilakumar, Email: moc.liamg@rkramukalina .

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Genetically Modified Foods (GMO), Essay Example

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Whether individuals are okay with it or not, we live in a world today where genetically modified foods (GMOs) are everywhere. What is meant by this is that unless an individual only eats organic foods day in and day out, he or she is invariably putting GMOs into his or her mouth every day. After becoming cognizant of this actuality, individuals often worry that they might not be buying the correct and safest products for their families. Therefore, it is imperative that all individuals become aware of the pros and the cons that come with GMOs. (WebMD)

To start off, individuals must come to grasps that at this time and age, it would be increasingly difficult to live a life eating only foods that do not contain GMOs. While this may seem alarming to some, there must be room for clarification as to what exactly are the purposes for GMOs. Often times, food is genetically modified for simple reasons, such as to grow grapes without seeds inside of them. However, other times, modifications are much more drastic, such as changing the color or the taste of a specific pepper. What this means is that scientists are able to acquire a desired taste by combining science with nature.

Despite the fact that there have been a variety of tests by the Food Administration in order to ensure that the food that farmers are growing is safe, there have been numerous reports where the food has not been reported in pristine condition. In general, it has been found that the consumption of a variety of foods with GMOs have been proven to increase the likelihood of an individual developing a food-based allergy. While this is not something grave, it is certainly something that should be taken a look at, given that a food that is being produced deliberately directly affects someone’s personal life. (“Pros and Cons of Genetically Modified Foods.” )

Genetically modified foods should not be regarded as dangerous, for individuals would never produce something that puts someone else’s life at risk. However, one should be cautious about what she decides to consume because of the fact that one does not always know what is inside the food that is being consumed.

A setback about producing GMOs is the fact that they do not have much economic value. This is due to the manner in which GMOs take just as long to grow as normal fruits and vegetables, amongst other foods. What this means is that there is no increase in production, so farmers do not have the ability to distribute their merchandise at faster pace. Perhaps the only advantage that GMOs would have within a market is that fact that they would prove to be great competition against other distributors. Other than that, however, GMOs could prove to be incredibly unprofitable.

An upside to GMOs is that often times, they contain more nutrients than the ordinary, unmodified product. This happens because when the fruits and/or vegetables are being modified, new nutrients must be injected into the foods in order to ensure that the foods will indeed be modified.

It is imperative that all individuals become aware of the pros and the cons that come with GMOs. Because of the fact that not many people are aware of what exactly they are putting into their mouths, it is the farmer’s and distributor’s responsibility that they are able to provide individuals with the best product that is available. One’s safety should never be put at risk just so that a profit can be made from selling something that will only make individuals sick. Therefore, individuals should be more wary of what they put into their mouths and consume.

Works Cited

“Pros and Cons of Genetically Modified Foods.”  HRF . HealthResearchFunding.org, 4 Dec. 2013. Web. 2 July 2015.

WebMD. “The Truth About GMOs: Are They Safe? What Do We Know?”  WebMD . WebMD, n.d. Web. 2 July 2015.

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The Arguments for Genetically Modified Food

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what are genetically modified foods essay

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The Tennessee State Capitol is seen Monday, Jan. 22, 2024, in Nashville, Tenn. (AP)

The Tennessee State Capitol is seen Monday, Jan. 22, 2024, in Nashville, Tenn. (AP)

Sofia Ahmed

A Tennessee bill doesn’t ban vaccines from being pumped into the food supply

If your time is short.

Tennessee House Bill 1984 would require food that contains vaccines to be classified as drugs by the Tennessee Department of Agriculture. It does not ban vaccines from food.

Edible vaccines, which are administered through food, have been in development since the 1990s but are not approved for use anywhere in the world. 

Learn more about PolitiFact’s fact-checking process and rating system.

A Tennessee bill that would designate vaccine-containing foods as drugs is being misleadingly characterized online.

"Tennessee has become the first State in America to ban Bill Gates’ toxic mRNA from being pumped into the food supply," read a screenshot of a news article posted April 6 on Facebook  reads. The screenshot included a photograph of Tennessee’s Republican governor, Bill Lee, signing papers. 

This post was flagged as part of Meta’s efforts to combat false news and misinformation on its News Feed. (Read more about our partnership with Meta , which owns Facebook and Instagram.)

Tennessee has not "banned" mRNA vaccines from food.  That’s partly because such edible vaccines — vaccines administered through foods — are not approved for use anywhere in the world, World Health Organization spokesperson Margaret Harris told PolitiFact.

The Facebook post’s screenshot is from a news article by The People’s Voice, a website that has spread misinformation before . The article refers to Tennessee House Bill 1894 , which would classify vaccine-containing foods as drugs. But that bill mentions neither Microsoft Corp. co-founder Bill Gates nor anything about mRNA being banned from the food. Gates is a frequent conspiracy theory target. In 2023, we fact-checked, and rated False , a claim that Gates was poisoning produce with chemicals.

H.B. 1894 "classifies any food that contains a vaccine or vaccine material as a drug." When discussing the bill during a Tennessee Senate session , state Sen. Joey Hensley, R-Hohenwald, said he knew of no specific examples of vaccine-containing food in Tennessee. But he said such foods are in development.

A legislative study said that if the bill became law there would be no associated costs because "there is no known test for these vaccines in food and no known lab doing this kind of analysis."

Although the U.S. Food and Drug Administration has not authorized use of edible vaccines, researchers are developing them in genetically modified foods such as potatoes, bananas, lettuce, corn and rice. 

Featured Fact-check

Researchers have long pursued edible vaccines as a cost-effective way to distribute, store and administer vaccines. The World Health Organization found they can be "produced cheaply in very high amounts." 

Charles Arntzen, a plant molecular biologist, was the first to produce a hepatitis B vaccine in tobacco in 1990. And, in 1998 , researchers supported by the National Institute of Allergy and Infectious Diseases reported the results of the first human trials of E. coli vaccines in potatoes. 

Despite these efforts, Arntzen said in 2004 that he hasn’t found vaccine manufacturers willing to finance larger human trials of edible vaccines. Edible vaccines vary by dose, which makes it difficult for regulatory agencies to approve them.

However, scientists are revisiting edible vaccines. University of California Riverside researchers, for example, announced in 2021 that they were studying whether mRNA vaccines can be administered through edible plants, such as lettuce.

The Tennessee House and Senate both approved H.B. 1894  April 8. Lee has not yet signed it into law. In Tennessee , if a bill is not signed by the governor after 10 days, it becomes law. 

The photograph of Lee signing a bill was first posted on Lee’s Facebook account in 2021, a reverse-image search found. 

We rate the claim that Tennessee has become the first state in the U.S. to ban Bill Gates’ mRNA from being pumped into the food supply False. 

RELATED: No, mRNA vaccines aren’t widely used in livestock and can’t get into the food supply  

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Facebook post ( archived ), April 6, 2024

The People’s Voice, Tennessee Bans Bill Gates’ mRNA From Food Supply , April 2, 2024

PolitiFact, No proof a study found lab-grown meat funded by Bill Gates causes ‘turbo cancer’ , Feb. 28, 2024

PolitiFact, Claims about the United Nations shunning Christians for not embracing pedophilia lack evidence , Aug. 11, 2023

PolitiFact, Study on possible COVID-19 brain effects looked at virus, not vaccines , May 18, 2023

Tennessee General Assembly, H.B. 1894 , accessed April 9, 2024

Tennessee General Assembly Fiscal Review Committee, Fiscal Note H.B. 1894 - SB 1903 , Feb. 3, 2024

Tennessee General Assembly, Senate Session - 56th Legislative Day , March 28, 2024

National Library of Medicine, Edible Vaccines , Oct. 22, 2013

U.S. Food and Drug Administration, Vaccines Licensed for Use in the United States , Dec. 1, 2023

Science Daily, First Human Trial Shows That An Edible Vaccine Is Feasible , April 30, 1998 

PolitiFact, No, mRNA vaccines aren’t widely used in livestock and can’t get into the food supply , Jan. 23, 2023

Tennessee General Assembly, How a Bill Becomes a Law , accessed April 9, 2024

Facebook post , May 14, 2021

Science Direct, Edible Vaccine , May 8, 2020

Nature Medicine, Edible vaccines not ready , Sep. 1, 2004

University of California, Grow and eat your own vaccines? , Sep. 16, 2021

Science Direct, Modern Applications of Plant Biotechnology in Pharmaceutical Sciences , 2015

World Health Organization, Plant-derived vaccines, accessed April 9, 2024

Email interview with Margaret Harris, World Health Organization spokesperson, April 9 - 11

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Guest Essay

Many Patients Don’t Survive End-Stage Poverty

In the upper right hand corner, two hands reach out for each other across a net; in the middle, a broken caduceus, one wing of which has fallen off; at the bottom, two faceless people sitting on the ground.

By Lindsay Ryan

Dr. Ryan is an associate physician at the University of California, San Francisco, department of medicine.

He has an easy smile, blue eyes and a life-threatening bone infection in one arm. Grateful for treatment, he jokes with the medical intern each morning. A friend, a fellow doctor, is supervising the man’s care. We both work as internists at a public hospital in the medical safety net , a loose term for institutions that disproportionately serve patients on Medicaid or without insurance. You could describe the safety net in another way, too, as a place that holds up a mirror to our nation.

What is reflected can be difficult to face. It’s this: After learning that antibiotics aren’t eradicating his infection and amputation is the only chance for cure, the man withdraws, says barely a word to the intern. When she asks what he’s thinking, his reply is so tentative that she has to prompt him to repeat himself. Now with a clear voice, he tells her that if his arm must be amputated, he doesn’t want to live. She doesn’t understand what it’s like to survive on the streets, he continues. With a disability, he’ll be a target — robbed, assaulted. He’d rather die, unless, he says later, someone can find him a permanent apartment. In that case, he’ll proceed with the amputation.

The psychiatrists evaluate him. He’s not suicidal. His reasoning is logical. The social workers search for rooms, but in San Francisco far more people need long-term rehousing than the available units can accommodate. That the medical care the patient is receiving exceeds the cost of a year’s rent makes no practical difference. Eventually, the palliative care doctors see him. He transitions to hospice and dies.

A death certificate would say he died of sepsis from a bone infection, but my friend and I have a term for the illness that killed him: end-stage poverty. We needed to coin a phrase because so many of our patients die of the same thing.

Safety-net hospitals and clinics care for a population heavily skewed toward the poor, recent immigrants and people of color. The budgets of these places are forever tight . And anyone who works in them could tell you that illness in our patients isn’t just a biological phenomenon. It’s the manifestation of social inequality in people’s bodies.

Neglecting this fact can make otherwise meticulous care fail. That’s why, on one busy night, a medical student on my team is scouring websites and LinkedIn. She’s not shirking her duties. In fact, she’s one of the best students I’ve ever taught.

This week she’s caring for a retired low-wage worker with strokes and likely early dementia who was found sleeping in the street. He abandoned his rent-controlled apartment when electrolyte and kidney problems triggered a period of severe confusion that has since been resolved. Now, with little savings, he has nowhere to go. A respite center can receive patients like him when it has vacancies. The alternative is a shelter bed. He’s nearly 90 years old.

Medical textbooks usually don’t discuss fixing your patient’s housing. They seldom include making sure your patient has enough food and some way to get to a clinic. But textbooks miss what my med students don’t: that people die for lack of these basics.

People struggle to keep wounds clean. Their medications get stolen. They sicken from poor diet, undervaccination and repeated psychological trauma. Forced to focus on short-term survival and often lacking cellphones, they miss appointments for everything from Pap smears to chemotherapy. They fall ill in myriad ways — and fall through the cracks in just as many.

Early in his hospitalization, our retired patient mentions a daughter, from whom he’s been estranged for years. He doesn’t know any contact details, just her name. It’s a long shot, but we wonder if she can take him in.

The med student has one mission: find her.

I love reading about medical advances. I’m blown away that with a brain implant, a person who’s paralyzed can move a robotic arm and that surgeons recently transplanted a genetically modified pig kidney into a man on dialysis. This is the best of American innovation and cause for celebration. But breakthroughs like these won’t fix the fact that despite spending the highest percentage of its G.D.P. on health care among O.E.C.D. nations, the United States has a life expectancy years lower than comparable nations—the U.K. and Canada— and a rate of preventable death far higher .

The solution to that problem is messy, incremental, protean and inglorious. It requires massive investment in housing, addiction treatment, free and low-barrier health care and social services. It calls for just as much innovation in the social realm as in the biomedical, for acknowledgment that inequities — based on race, class, primary language and other categories — mediate how disease becomes embodied. If health care is interpreted in the truest sense of caring for people’s health, it must be a practice that extends well beyond the boundaries of hospitals and clinics.

Meanwhile, on the ground, we make do. Though the social workers are excellent and try valiantly, there are too few of them , both in my hospital and throughout a country that devalues and underfunds their profession. And so the medical student spends hours helping the family of a newly arrived Filipino immigrant navigate the health insurance system. Without her efforts, he wouldn’t get treatment for acute hepatitis C. Another patient, who is in her 20s, can’t afford rent after losing her job because of repeated hospitalizations for pancreatitis — but she can’t get the pancreatic operation she needs without a home in which to recuperate. I phone an eviction defense lawyer friend; the young woman eventually gets surgery.

Sorting out housing and insurance isn’t the best use of my skill set or that of the medical students and residents, but our efforts can be rewarding. The internet turned up the work email of the daughter of the retired man. Her house was a little cramped with his grandchildren, she said, but she would make room. The medical student came in beaming.

In these cases we succeeded; in many others we don’t. Safety-net hospitals can feel like the rapids foreshadowing a waterfall, the final common destination to which people facing inequities are swept by forces beyond their control. We try our hardest to fish them out, but sometimes we can’t do much more than toss them a life jacket or maybe a barrel and hope for the best.

I used to teach residents about the principles of internal medicine — sodium disturbances, delirium management, antibiotics. I still do, but these days I also teach about other topics — tapping community resources, thinking creatively about barriers and troubleshooting how our patients can continue to get better after leaving the supports of the hospital.

When we debrief, residents tell me how much they struggle with the moral dissonance of working in a system in which the best medicine they can provide often falls short. They’re right about how much it hurts, so I don’t know exactly what to say to them. Perhaps I never will.

Lindsay Ryan is an associate physician at the University of California, San Francisco, department of medicine.

Source photographs by Bettmann and Fred W. McDarrah via Getty Images.

The Times is committed to publishing a diversity of letters to the editor. We’d like to hear what you think about this or any of our articles. Here are some tips . And here’s our email: [email protected] .

Follow the New York Times Opinion section on Facebook , Instagram , TikTok , WhatsApp , X and Threads .

Should All Genetically Modified Foods Be Labeled?

Introduction, arguments against labeling of genetically modified food, arguments in support of labeling of genetically modified food, works cited.

Genetically modified food has become a controversial topic in the current society. According to Marchant (75), the world has been experiencing changes in weather patterns due to issues of global warming. As a result of this, agriculture has been massively affected. On the other hand, the world population is constantly on the rise.

The number of those who practice agriculture is also decreasing. This is because people move to towns to get employed in large manufacturing companies or the retailers. This means that there is an increased pressure on the farmers to come up with a solution for this challenging situation. According to Sateesh (87), the solution that farmers were looking form came at last with the help of advanced technology.

Genetically modified organisms were proven to be more productive than natural products. Genetically modified plants were more resistant to drought and could produce more than the natural plants. Genetically modified animals took much shorter time to mature, and those that produce milk would be yielding more milk when the breed is genetically modified. This was a breakthrough discovery in the field of agriculture. Farmers were given a solution to the problem of increasing productivity of their crops.

The society welcomed the breakthrough for it was convinced of having a reliable source of food throughout the year at affordable prices. Many members of the society considered this invention as the best way through which the food security would be assured. This was till it was discovered that genetically modified food could have a negative effect on the human being when consumed. According to Weiss (46), genetically modified foods may have an effect on the genetics of a human being.

The effect may not be exhibited immediately. It may take years of regular consumption of genetically modified food for the effect to be seen. In some instances, the effect may be witnessed on the children of the regular consumers of genetically modified food. People consuming this product should, therefore, be aware of these consequences. They should be informed every time they purchase genetically modified food, that the product is not natural.

There has been a strong argument against labeling of the genetically modified foods. There is a section of the society that has come out strongly to oppose any move that would compel manufacturers to label their products. The leading defenders of lack of labeling genetically products are the manufacturers. Manufacturers have come out to reject the clarion call that all the genetically products should be clearly labeled before they are put on sale. These manufacturers have cited the cost of the labeling process as being high.

These manufacturers believe that labeling genetically modified food would force the prices to increase their prices as a way of passing the cost to the customer. According to Davida (34), this argument has always been supported by some members of the public who are the consumers. According to this scholar, members of the public are always comfortable with the idea of not labeling the genetically modified food.

They share the idea of the producers that such processes would always increase the cost of the product which they are not ready to pay. It is a fact that through genetically modified foods, the price of food has gone down considerably. The consumers have come to appreciate the positive impact that genetically modified food has brought into their lives ever since it was discovered.

A section of the society still believes that genetically modified foods are as safe as other naturally grown products. According to Weiss (124), some scientists have been advocating for the use of genetically modified food not only because it is cheap to produce, but also because it is a safe product.

This argument has seen a section of society reject the idea of labeling genetically modified food. They argue that labeling of the genetically modified food would raise unnecessary concern within the society. As such, they believe that the products should not be labeled. Sateesh (87) says that labeling of the genetically modified foods will be like condemning these products in the market for no good reason.

This scholar says that the move will not act as an attraction of customers towards the product but a repellant. This scholar says that the tag will act as a warning that is given to the customers saying that they should be duly informed that the product they are purchasing is not a normal product. The message will be saying that the product has abnormal genes that may have a direct negative impact on their lives. Customers will always shy away from such products. They will consider them unfit for consumption.

The producers of such products will, therefore, be driven out of the market. This comes with serious consequences to the technological inventions and innovations in the market. The scientists who were involved in this technology will be forced to stop further exploration in this field because of public rejection.

With the current trend, those who are opposed to labeling of this product say that the world population will be double the current population. This will have a massive consequence on food production. With this huge population, these people argue that it is only genetically modified foods that can sustain them. When genetically modified foods are discriminated against, and the technology is brought to its knees, there will emerge a serious food problem in the society in the near future.

These people, therefore, insists that the society should learn to appreciate the importance of this technology in food production. Such unnecessary and discriminatory policies as labeling of the genetically modified foods should be stopped in order to help advance this technology and assure the population of constant and reliable food production.

Labeling of the genetically modified food should not be an issue that raises controversy the way it does. The society has lived in a transparent manner in terms of what we eat ever since the modernization age. When one walks into a hotel, one would order a simple meal like beans and rice for lunch.

This individual would not expect to be given meat pie and rice, or any other product that is not paid for. According to Food, Drug and Cosmetics Act of 1938, all food substances should be labeled (Nelson 76). This Act demands that all food substances should have all the ingredients labeled so that the consumers would know what they are purchasing before they can consume the product.

This Act is supported by the Nutrition Labeling and Education Act of 1990 which demands of labeling of all food ingredients. These are laws observed within the United States of America. These laws have not been changed. Genetically modified foods have a different genetic modification from the normal products. This is a substantial reason that should make them be labeled differently from other products.

The law should not be applied selectively, and neither should it be undermined. When a manufacturer of bread adds eggs to his or her bread and fails to indicate that the bread has eggs as one of the ingredients, such a person would be liable for prosecution. The courts would send him or her to prison for several years for contravening the law. Those who produce genetically modified food should also be subjected to the same law because they are committing the same crime. The law should be fairly administered.

A section of the scientists has reported that genetically modified food have negative consequences that are still unknown to them. These scientists argue that genetically modified foods contain some genes which have some serious negative consequences on the health of consumers.

These scientists have embarked on a massive research to try and unearth some of the consequences of genetically modified foods on people. While these researchers are still working on this issue, the society should be given a choice to decide on whether they will consume genetically modified food or not. The choice can also be made when the products are labeled. Labeling of the products helps ensure that a consumer will be aware that a given food substance is genetically produced while others are not.

Although it has been difficult to determine the effect of genetically modified food, recent research of the effect of genetically modified food has shown a worrying trend that this food have on animals. The study, which was conducted on rats, showed that the genetically modified foods cause sterility on rats after three generations. This shows that when the first generation consumes genetically modified food, they are not affected by it and, therefore, shall reproduce normally.

The second generation will also be safe. In the third generation, reproduction will be impossible because the genetics of this organization in the third generation shall have been massively affected. Genetically modified foods were introduced about 20 years ago. This means that the current population is still in the first generation. They may not feel the effect of genetically modified food. Their children who will be the second generation may also not have problems with reproduction.

The problem will start in the third generation, when we are to base the reasoning on the results that these scientists have given (Okumu 78). This is enough reason to inform consumers that the product they are consuming is genetically modified. If the consumer is to base his or her reasoning on the recent research reports, then he or she would try avoiding these products. This can only be possible if the products are clearly labeled.

One of the main reasons why consumers like their food labeled is because of the nutrition they get from these foods. There are consumers who are under medication. Such consumers would have prescribed nutrients that should be gotten from some foods. Such individuals would always rely on labeling of the ingredients in order to ascertain the quality of food eaten.

This can only be possible if they are given all the ingredients of their food on the label. Failure to do this will be condemning them. This may affect them negatively. This will be contravening the law which demands that all the genetically modified foods should be labeled.

Research has also shown that genetically modified foods come with an allergy to the animals. They attribute this to the introduction of foreign proteins in the genetically modified food. This may explain the constant rise in allergy problems among the American populace. The recent rise in immune disorders can possibly be attributed to consumption of genetically modified foods. For the purpose of clarity, it would be important to label these genetically modified foods so that the consumer can choose whether to purchase these products or not.

According to Sateesh (92), it is a fact that the use of pesticide has increased with the introduction of the genetically modified foods. According to this scholar, scientists have proven beyond any doubt that when using genetically modified crops, there should be an increase in the use of pesticides in order to protect the crops.

This is because these crops are prone to some forms of pests. In order to avoid pest destruction, there has to be a constant use of pest. The pesticides are not only necessary when the crop is at the farm. The pesticide should also be in use when the crop is in the store waiting for the delivery to the consumer. This means that a consumer will be buying a product that has a heavy presence of pesticide. Pesticides are chemicals meant to kill pests. In its simplest definition, pesticides are poisons.

When a consumer buys such a poisonous product, it needs no scientific genius to know that the effect will be massively destructive. The consumer may not realize this instantly (Rudisill 220). This is because he or she will be consuming small quantities of the poison every time he eats the product. When one takes the poison in small quantities consistently, and for a long time, it will bring out its effect. In most of the cases, it is always too late to help such an individual. The poison shall have taken its toll on him or her.

Most of the European countries have genetically modified crops in their countries. They cite the negative impact that genetically modified crops have on the health of consumers. France for instance, has banned growing of genetically modified crops because of the possible cross pollination.

The genetically modified crops would cross pollinate with the non-GMO plants. This will make the final product have the effects of the GMO. For this reason, the governments of most of the European countries have banned the use of genetically modified crops. In the United States, the treatment is very different. The government has not issued an official ban on the sale of, or growing the genetically modified crops.

This is because of the democracy that the government feels that the farmers should be allowed. However, this genetically modified food should be clearly labeled so that one would be aware. If these European countries could issue a total ban on genetically modified crops, and their sale, then the citizens of the United States should have at least some right to know the products that are genetically produced. This would give them the freedom to make the choice of either consuming the products or not.

The involvement of Monsanto Company in the opposition to the move to label the genetically modified foods leaves a lot to be desired. According to Nelson (87), this company is known for its self interest and the need to reap maximally from the public without giving any attention to the demands of the public. This scholar reports that Monsanto was on the front line trying to fight farmers who were not willing to move the GMO way.

This was because they were the leading sellers of the genetically modified seeds to the farmers. To them, those farmers that were reluctant in adopting the new technology were dragging food production in this country. In essence, this company was fighting these farmers because of its own selfish interests. This scholar also brings back the memory of this firm assuring the public of the safety of Agent Orange and DDT as safe products that could be used as household items (Lenaola 46).

Given the fact that at that time it had won the trust of the public, the American public was convinced that these products were safe for use domestically. Monsanto was then considered as one of the companies that were determined to transform the society positively through innovation and inventions in the field of agriculture. This trust did eliminate any doubt that the public could have on the use of the two products which then became common household items.

After a long period of over one year, scientists would later discover that these products were not safe for domestic use. This was after the public had been massively affected, and there was an increase in issues related to health among the heaviest users of this product. This was an unethical behavior exhibited by this firm. There was no direct heavy consequence that the government laid on this firm even after it was confirmed that it had misled the public and caused health complications on some.

Lastly, ethics demands that when in the market, transparency is of utmost importance. It is important to ensure that all the products sold to the public are of known ingredients and from known sources.

When selling food substance to the public, Weirich (114) says that one should realize the fact that this food will have a direct effect on his or her health. The government may not have banned the sale of genetically modified crops in this country. However, there are some individuals who strongly believe that they cannot consume genetically modified foods.

It would be fair to inform such individuals through labeling, that these are genetically modified products. Such an individual would make a personal decision on whether to consume this product or not. It is also intriguing why the producers of genetically modified crops are strongly opposing the need to label their products, while at the same time insisting that they are safe. If they are safe as they proclaim, then let them be labeled.

There has been a massive debate as to whether or not genetically modified foods should be labeled or not. The proponents and opponents of this move have given their reasons with equal force. However, the world of today demands that ethics should be maintained. Revealing the ingredients of food products is one such ethical requirement. Before one eats a given food, he or she should know all the ingredients. For this reason, all the genetically modified foods should be labeled clearly.

Davida, Kenneth. What Can Nanotechnology Learn from Biotechnology? Social and Ethical Lessons for Nanoscience from the Debate Over Agrifood Biotechnology and Gmos . Amsterdam: Elsevier, 2008. Print.

Lenaola, Valorie. “The Need to Label Genetically Modified Food.” The Journal of Nutrition 35.1 (2008): 37-56. Print.

Marchant, Gary. Thwarting Consumer Choice: The Case against Mandatory Labeling for Genetically Modified Foods . Washington: AEI Press, 2010. Print.

Nelson, Gerald. Genetically Modified Organisms in Agriculture: Economics and Politics . San Diego: Academic Press, 2001. Print.

Okumu, Paul. “Labeling Genetically Modified Food.” The Philosophical and Legal Debate . 56.2 (2007): 26-79. Print.

Rudisill, Careen. “Are Feelings of Genetically Modified Food Politically Driven?” Risk Management Attitudes and Behaviour 10.3 (2008): 218-234. Print.

Sateesh, Macbeth. Bioethics and Biosafety . New Delhi: I.K International Pub. House, 2008. Print.

Weirich, Paul. Labeling Genetically Modified Food: The Philosophical and Legal Debate . Oxford: Oxford University Press, 2007. Print.

Weiss, Edith. Reconciling Environment and Trade . Leiden: Martinus Nijhoff Publishers, 2008. Print.

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  22. Opinion

    I'm blown away that with a brain implant, a person who's paralyzed can move a robotic arm and that surgeons recently transplanted a genetically modified pig kidney into a man on dialysis. This ...

  23. Is Genetically Modified Food Safe for Human Bodies and the ...

    History of Genetically Modified Foods. Genetically modified crops were produced for the first time in 1980s. The earliest bio-modified food to arrive at the supermarket was the Flavr Savr tomato, which was standardized in 1994. With a particularly solid hide, the Flavr Savr guaranteed a longer shelf existence than nearly all tomatoes (Zinnen 31).

  24. Safety evaluation of an extension of use of the food enzyme peroxidase

    The food enzyme peroxidase (phenolic donor: hydrogen-peroxide oxidoreductase, EC 1.11.1.7) is produced with the genetically modified Aspergillus niger strain MOX by DSM Food Specialties B.V. A safety evaluation of this food enzyme was made previously, in which EFSA concluded that this food enzyme did not give rise to safety concerns when used in one food manufacturing process.

  25. Should All Genetically Modified Foods Be Labeled?

    These laws have not been changed. Genetically modified foods have a different genetic modification from the normal products. This is a substantial reason that should make them be labeled differently from other products. The law should not be applied selectively, and neither should it be undermined.