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Genetically modified (GM) foods

In 1998, American biotech company Monsanto launched a GBP 1m advertising campaign to convince the British public that GM food was safe. Their "Food, Health and Hope" campaign claimed that they had conducted "rigorous tests" over 20 years to ensure that their crops were "as safe and nutritious as the standard alternatives." Following a wave of complaints, the Advertising Standards Authority condemned the adverts for being "confusing, misleading, unproven and wrong." [119]

For a glossary of terms relating to GM foods, click here

GM foods have not been adequately tested

In 2001, a Joint FAO/WHO Expert Consultation on Allergenicity of Foods Derived from Biotechnology detailed a protocol for evaluating the allergenicity of GM foods.[122] No GM crops currently available on the US market have been assessed by either the FDA (Food and Drug Administration) or the EPA (Environmental Protection Agency) using this protocol.

In 2002, the Codex Alimentarius Ad Hoc Task Force on Foods Derived from Biotechnology agreed on a "Draft guideline for the conduct of food safety assessment of foods derived from recombinant-DNA plants."
[123] Thirty five countries, including the US, agreed on this document and recommended that it be adopted by the full Codex Alimentarius Commission. In the case of trade disputes, the World Trade Organization considers that, in terms of food safety, the standards or guidelines of Codex Alimentarius are deemed the global science-based standard and, thus, immune to trade challenges, i.e. they are not considered to be a non-tariff trade barrier. At present, the US has not subjected GM maize to the complete safety assessment laid out in this document.

The FDA does not require safety testing for GM crops and has not formally approved any of the GM corn varieties being grown in the US.
[120] Instead, the FDA conducts "voluntary safety consultations" with companies, allowing them to carry out their own testing.

An example can be seen in a letter from the FDA to Monsanto on the safety of its MON810 Bt corn: "Based on the safety and nutritional assessment you have conducted, it is our understanding that Monsanto has concluded that corn grain and forage derived from the new variety are not materially different in composition, safety, or other relevant parameters from corn grain and forage currently on the market, and that they do not raise issues that would require premarket review or approval by FDA."
[121]

Correspondence between the FDA and Calgene on the safety of the GM FlavrSavr tomato (see below) shows that, even when the company finds health problems in animal tests, the food is still released onto the market without any need for labeling.
Consumers International reports that the letters for all 52 "safety consultations" done since the Flavr Savr tomato contain basically the same language, i.e. the FDA simply repeats what the biotech company has told it, without any independent testing.
[120]



Substantial equivalence

"Substantial equivalence" is a legal concept invented by the biotech industry. GM companies claim that a GM food is "substantially equivalent" to (i.e. "the same as") the non-GM version, and therefore does not require labels or extensive testing. It is, however, substantially different enough to allow patenting.

Substantial equivalence is an unscientific concept that has never been clearly defined, and there are no legally binding rules on how to establish it.
[124]

Corporate testing

Health-risk assessment of GM foods compares only a few known factors (e.g., some nutrients, known toxins and allergens) between GM and the equivalent non-GM crop. If these limited factors are similar, then the two foods are assumed to be substantially equivalent and therefore safe.

Short-term animal feeding trials are conducted in some cases, but there is no requirement for human trials for either toxicity or allergy testing. No independent testing or checks of the company's claims are required.

Genetic engineers usually avoid testing whole foods. Instead, they try to isolate the modified part of the food and test that. However, the modified protein is usually present in the food at very low concentrations, if at all. This makes it difficult to collect enough of the protein to test it, so researchers put the foreign gene, known as a 'transgene,' into bacteria, which can produce large amounts of protein very quickly, and test that instead.[125]

This is completely meaningless for at least three reasons. First, different species do not process genes in the same way. In the cells of every living creature is the machinery to translate genes into proteins, but like three different factories that use the same raw material (soybeans) to produce tofu, biofuel and fabric, the 'factories' inside bacteria, plants and animals turn the same starting material (genes) into very different proteins. They have different processing machinery in their cells and, like the disastrous pregnancy drug thalidomide, even small differences in processing can cause a major difference in the function of the final product.

Second, the transgene is not the only potentially harmful change produced during genetic modification. When a transgene is inserted into animal or plant chromosomes, its position is random. It may disturb or destroy an existing gene. Genes do not work independently, but in highly complex relationships which are not fully understood. Any change to the DNA at any point will affect it throughout its length in ways that cannot be predicted, even by biotechnologists.

Third, in addition to the transgene, genetic engineers must also introduce other genes or pieces of DNA to control or monitor it, including promoters, transcription terminators, antibiotic resistance marker genes and reporter genes. Data on the safety of these are scarce, even though they can affect the safety of the GM crop.
[129]

Genetic engineering is not the same as traditional breeding

In traditional breeding, plants or animals with desirable traits such as good flavor or resistance to disease are chosen for breeding, and their genes reproduced naturally through mating. Corn can cross-pollinate with corn and pigs can mate with pigs, but it would be impossible for a tomato to reproduce with a fish, for example.

But with genetic engineering, genes can be 'cut and pasted' in a way that would never occur naturally by breeding, to create new species that have never existed before. For example, a gene from a salmon could be introduced into a potato, extra copies of a 'growth gene' could be inserted into a chicken to make it grow bigger, faster, or a gene to produce a pesticide could be introduced into maize.


Genetic engineering can introduce transgenes which have never before been part of the food chain, such as a transgene from a non-farm animal, a bacteria or virus, a flower or even from humans, and their effect on the human body is unknown.


The evidence

No GM foods approved for human consumption have undergone long-term feeding trials in animals or humans. Biotech giants
53% of Europeans would pay more for non-GM food.[126]
66% of Europeans would not buy GM food even if it tasted better, and would not eat eggs from hens fed GM maize.[126]
95% of EU citizens want the right to choose and 71% simply do not want GM food.[126]
Less than a third of UK consumers thought the idea of food produced from a GM plant acceptable while 45% said they try to avoid GM food and ingredients. 64% were concerned they could be eating GM ingredients without knowing it.
claim that they have done "rigorous testing" into the safety of GM foods, but this alleged data cannot be found in any peer-reviewed scientific journal.[127] Requests for safety data are labeled "hysterical," and concerned consumers are "anti-science luddites" or "uninformed technophobes." GM giants often make public calls for "open debates based on science," but several researchers and journalists with scientific evidence questioning the safety of GM products say that these companies have bribed, threatened, censored and intimidated them into keeping quiet.

Only one scientific study on human consumption of GM food has been published in a peer-reviewed journal, and it showed alarming results after a very short time. Other studies on animals and anecdotal evidence have shown that GM foods can cause allergies, rare disorders, disabilities and death. Even animals choose not to eat it.


Spud u dislike

In 1998, Dr Arpad Pusztai sparked a long running controversy after he revealed the results of his experiments at the Rowett Research Institute in Scotland, which indicated that GM potatoes had harmed rats.
[128]

After rats were fed GM potato containing a snowdrop transgene for just 10 days, Dr. Pusztai found increases in the thickness and length of some sections of the stomach and intestines. He also saw indications of a weakening of the immune system.

However, these effects were not due to the transgene. Pusztai's team discovered that the changes were due to the 'extra' DNA that is inserted during genetic engineering. Specifically, they believed the changes were due to the promoter.

A promoter is a short piece of DNA at the beginning of a gene which acts like an on/off switch. The promoter in the GM potato was taken from the cauliflower mosaic virus - the same promoter which is used in GM tomato paste, soya oils and maize found in hundreds of products on supermarket shelves.

Following Dr Pusztai's revelations in a television interview, which had been authorized by his employers, his work was confiscated, he was forced to retire and was banned from publicly speaking about his work. The editor of The Lancet, a leading British medical journal which was due to publish his data, was allegedly threatened by a senior member of the Royal Society that his job would be at risk if he published controversial research.

Another team of scientists who had looked at the same GM protein used in Dr Pusztai's potatoes found that it binds to human white blood cells.

Guts

In the world's first known trial of GM food on human volunteers, published in the British Journal of Nutrition, GM DNA was found to move into human gut bacteria, raising serious health questions.
[130]

After eating just one meal of a burger and milkshake containing commercial GM soya and maize, the GM DNA survived passage through the small intestine and moved into bacteria in the gut. In three out of seven samples, researchers found bacteria had taken up the herbicide-resistance transgene from GM food at a very low level.

Like the promoter in the GM potato experiments, many GM crops have antibiotic-resistance "marker genes" inserted into them. These are extra genes that 'mark' the DNA and give scientists an easy way to identify GM cells or tissues.

Movement of transgenes between species can create new viruses and bacteria that cause diseases, spread drug and antibiotic resistance and trigger cancer by jumping into the DNA of mammalian cells.[131]

If DNA from antibiotic-resistance marker genes can find its way into the human stomach, as the human experiment suggests, then people's resistance to widely used antibiotics could be compromised.

In 2002, the British Medical Association (BMA) called for an end to field trials of GM crops because of fears that these antibiotic-resistance genes could move into non-GM plants and "possibly into pathogenic organisms causing human disease."

It is already known that GM DNA in the diet can move into organs around the body. Researchers at the University of Cologne, Germany, have found that when mice were fed GM DNA, the DNA was found in the gut wall, intestine, white blood cells, spleen and liver. When fed to pregnant mice, the DNA passed into the placenta, fetus and remained in the newborn mice.[131]




Moving transgenes

The movement of transgenes from food into bacteria or viruses has huge potential for creating new diseases. Viruses containing transgenes could cause famine by destroying crops or cause human and animal diseases of tremendous power. The widely used cauliflower mosaic virus (present in the GM potatoes used by Dr. Pusztai and in commercial tomato paste, soy and maize) is a potentially dangerous gene. It is very similar to the Hepatitis B virus and related to HIV.

There has already been one known human victim of the movement of a transgene between species. A French boy developed leukemia last year after a transgene used in a controversial 'gene therapy' to cure severe combined immune deficiency (SCID) inserted itself into one of his chromosomes. The therapy involved removing bone marrow cells from his hipbone, infecting them with a GM virus containing a transgene that is present in healthy children but missing in children with SCID, then returning the cells to the body. However, the transgene moved into one of the boy's chromosomes and disrupted a gene involved in the development of blood cells. The result was completely random and unpredictable.

Renowned geneticist Dr. Mae-Wan Ho has also suggested that the deadly E. coli 0157:H7 bacteria, which was not known to exist before 1982, was created when the genes to make the powerful shiga toxin (from the bacteria Shigella) moved into a more harmless strain of E. coli.[132]

FlavrSavr

In May 1994, the FDA announced that FlavrSavr, a tomato genetically engineered by Calgene to delay softening, was as safe as tomatoes bred by conventional means. "We have approached our review of this product with scientific rigor and a commitment to full, public disclosure of that science," said FDA Commissioner Dr. David Kessler. "Consumers can be confident that we remain committed to assuring that foods produced by genetic engineering are as safe as food in our grocery stores today."
[133]

This is in complete contrast to an FDA internal memo dated June 16, 1993. A "wholesomeness" study conducted by Calgene had found gross lesions in the stomachs of four out of twenty female rats fed GM tomato for 28 days. Male rats did not have lesions.
[134] Seven out of forty rats fed Flavr Savr died within two weeks for unstated reasons.[129]

In humans, this type of lesion could lead to a life-threatening hemorrhage, especially in elderly people who use aspirin to prevent thrombosis.

However, Calgene claimed there were no significant differences in total protein, vitamins and mineral contents and in toxic glycoalkaloids. Therefore, FlavrSavr and non-GM tomatoes were "substantially equivalent."

Calgene dismissed the lesions as "incidental," and as of December 10, 1993, had neither further addressed nor explained them. The FDA does not mention this in its "Evaluation of the FlavrSavr Tomato" report on its website,
[135] and did not find it necessary to require special labeling of FlavrSavr.[133] Calgene's tests have not been peer-reviewed or published.

Ironically for a tomato named "FlavrSavr," Belinda Martineau, a member of Calgene's original research team, admitted that "the flavor wasn't really there."
[136] So what was the point?



GM crops kill wildlife

A type of potato genetically modified to produce a pesticide also harms beneficial predator insects such as ladybirds. The pesticide/potato was designed to kill aphids which feed on the crop, but research by the Scottish Crop Research Institute found that when ladybirds were fed aphids which had eaten the GM potato, the ladybirds' lifespan was cut in half and reproduction was adversely affected.
[137]
Kent Loeffler, Cornell News

Bt corn contains transgenes from the bacterium Bacillus thuringiensis (Bt) which produce a toxin that kills the European corn borer, a major corn pest. However, it also kills monarch butterfly larvae, which are not a threat to crops.[138]

The toxin produced by the transgene is also present in the pollen. When this pollen is dispersed by the wind, it lands on other plants, including milkweed, the sole food of monarch caterpillars and commonly found around cornfields. When caterpillars feed on milkweed leaves dusted with the GM pollen, they eat less, grow more slowly and nearly half of them die.

The pollen can be blown more than 60 yards from the edge of cornfields.


GM food supplements kill people

Tryptophan is an essential amino acid present in food and available as a food supplement. Supplements are produced by harvesting the amino acid from bacterial cultures.

The manufacturers of one brand of tryptophan sold in the US utilized GM bacteria to increase yields, and found themselves on the receiving end of US$ 2 billion worth of claims. The GM bacteria had generated a new toxin which caused 5,000-10,000 people to fall ill with EMS (eosinophilia-myalgia syndrome), killed at least 37 people (possibly hundreds more) and permanently disabled 1,500.
[139] Tryptophan harvested from non-GM bacteria did not cause these problems.

The toxin had not been detected by the company because it was completely new, generated by the process of genetic engineering. The problem was discovered because EMS is a highly unusual illness, but had the tryptophan produced a more common ailment, such as an allergy or asthma, it could have been easily overlooked.

The company was not required to test the GM version of L-tryptophan because of the assumption that it was "substantially equivalent" to the non-GM version.




Chicken feed

GM corn (T-25) currently growing in Britain was found to increase the number of deaths of chickens which fed on it. A study comparing T-25 GM and non-GM corn found that twice as many broilers fed the GM maize died compared with those fed the non-GM maize.
[140]

Despite this, Acre (Advisory Committee on Releases to the Environment) granted approval for the commercial use of T-25 in 1996.

Even animals don't want GM food

Canadian farmers store GM and non-GM grains in separate bins, but whereas the non-GM bins are full of mice, the mice avoid the GM bins.
[141] Farmers in Holland have found the same, and a Dutch undergraduate student did an experiment to prove that mice definitely prefer non-GM.[142]

Geese will not eat GM canola, and will avoid GM fields in favor of non-GM fields.

In contrast, when given a choice between conventional and organic foods, it seems that at least some animals prefer the latter.

Zookeepers at Copenhagen Zoo report that tapirs and chimpanzees systematically choose organic bananas and fruits, rejecting the non-organic foods left in their cages. They also eat the organic bananas with their skins on, but always peel non-organic bananas first.
[143]

A Ph.D. thesis carried out at the Ludwig Boltzmann Institute for Biological Agriculture by Irene Edelmuller, showed that rabbits prefer organic to conventional feed.

Mice prefer organically grown wheat 90 percent of the time.
[144]

Earthworms repeatedly migrate away from a box with soil with mineral fertilizers to one with organic compost.[144]

Significantly more hens prefer beets that were organically grown.
[145]



Allergies

One of the greatest concerns about GM foods is their potential to increase allergies and anaphylaxis.

There are no reliable ways to test GM foods for allergies. If the transgene is from a food known to cause allergies in humans, such as shrimp, wheat or peanuts, then the final GM product can be specifically tested for that allergy. However, even a gene from a non-allergenic food may become allergenic in a different species because of the different processing machinery. And a gene from a non-food source, such as a bacterium or a human, could produce allergies never seen before. And if it is unknown, it cannot be tested for. Like the novel toxin created by GM L-tryptophan production, a novel allergen may be created through GM foods.

Nuts

A US company introduced transgenes from Brazil nuts into soybeans to increase the level of sulphur-rich protein.
[146] But tests found that the protein did not form properly in the soybeans and could cause allergies in humans.[147] The soy had been intended for use as chicken feed, but the company abandoned the project, saying it was difficult to prevent the protein from entering the human food chain.[148]

Other known allergens have also been inserted into food crops: the allergen ?-casein from cow's milk has been inserted into soybean and glycinins from soy into rice.[149]

Bt corn

One of the first steps in checking if a protein can cause an allergy is to determine if it has a similar structure to a known allergen. The toxin produced by Bt corn, which kills the monarch larvae, has been found to have a similar structure to vitellogenin (which can cause allergies from egg yolks) and b-lactoglobulin (which causes allergies from milk).
[120]

Another way to determine if a protein can cause an allergy is to test humans or animals for antibodies to it. If antibodies are present in human blood, it is likely that the protein is allergenic. A study of farm workers who worked in onion fields where Bt sprays were used found that two of them contained antibodies to Bt toxin.


StarLink

Dr. Chin Osoth, former Secretary-General of the Thai Health Ministry, reported that he and another member of his family developed allergies after eating a processed snack suspected of containing GM ingredients. When he stopped eating the snack, his rash went away. When he started eating it again, his eyes became inflamed.

His story is similar to at least 44 Americans who reported allergies after eating one of over 300 processed foods which became contaminated with the now infamous GM StarLink corn. Starlink was supposed to be used as an animal feed and was unapproved for human consumption, but managed to work its way into the human food supply.



GM references
[119] Guardian (11 August 1999). Monsanto GM food ads found to mislead.
[120] Hansen, M. for Consumers International (10 January 2003). Government lack of safety standards for GM crops revealed. Media briefing, Brussels.
[121] Letter from the FDA to Monsanto regarding Bt corn.
[122] Evaluation of Allergenicity of Genetically Modified Foods. Report of a Joint FAO/WHO Expert Consultation on Allergenicity of Foods Derived from Biotechnology. 22 - 25 January 2001.
[123] Codex Alimentarius. (2002). Ad Hoc Intergovernmental Task Force on Food Derived from Biotechnology. (ALINORM 03/34).
[124] Millstone, E., Brunner, E. and Mayer, S. (1999) Beyond substantial equivalence. Nature. 401; 525-526.
[125] MacKenzie, D. (17 April 1999). Genetically manipulated food cannot be reliably tested: Unpalatable truths. New Scientist.
[126] INRA (Europe) ECOSA (2000). Eurobarometer 52.1: The Europeans and Biotechnology.
[127] Vint, R. The mystery of the missing research on GM food. Genetic Food Alert.
[128] Ewen, S.W.B. and Pusztai, A. (1999). Effect of diets containing genetically modified potatoes expressing Galanthus nivalis lectin on rat small intestine. The Lancet. 354 (9187).
[129] Pusztai, A. (2001). Genetically Modified Foods: Are They a Risk to Human/Animal Health? ActionBioscience.org.
[130] Mart?n-Or?e, S.M. et al. (2002). Degradation of transgenic DNA from genetically modified soyabean and maize in human intestinal simulations. British Journal of Nutrition. 87(6); 533-542.
[131] Mae-Wan, H. (2002). Stacking the Odds Against Finding It. Science in Society, issue 16.
[132] Mae-Wan, H. (2001). E. coli 0157:H7 and Genetic Engineering. Science in Society.
[133] Access Excellence at the National Health Museum. (1994). The Flavr Savr Arrives.
[134] Alliance for Biointegrity. Key FDA documents revealing (1) Hazards of genetically engineered foods, and (2) Flaws with how the agency made its policy.
[135] FDA'S Policy for Foods Developed by Biotechnology. Evaluation of the FlavrSavr Tomato.
[136] Living on Earth (2001). FlavrSavr.
[137] Birch, A.N.E. et al. (1999). Tri-trophic interactions involving pest aphids, predatory 2-spot ladybirds and transgenic potatoes expressing snowdrop lectin for aphid resistance. Molecular Breeding. 5 (1); 75-83.
[138] Losey, J.E., Rayor, L.S. and Carter, M.E. (1999). Transgenic pollen harms monarch larvae. Nature. 399; 214.
[139] Mann, L.R.B., Straton, D. and Crist, W.E. (1999). The Thalidomide of Genetic Engineering. Soil and Health.
[140] BBC (27 April 2002). GM safety tests "flawed."
[141] Mae-Wan, H. (2002). Canadian Farmers against Corporate Serfdom. Science in Society, issue 16.
[142] Mae-Wan, H. Mice Prefer Non-GM.
[143] Islam Online (27 January 2003). Monkeys at Copenhagen Zoo go ape over organic bananas.
[144] Pfeiffer, E.E. (1938). Soil Fertility, Renewal, and Preservation. New York: Trans. F. Heckel. Anthroposophic Press.
[145] Plochberger, K. (1989) Feeding Experiments - A Criterion for Quality Estimation of Biologically and Conventionally Produced Foods. Agricultural Ecosystems & Environment. 27; 419-428.
[146] Jones, L. (1999). Science, medicine, and the future: Genetically modified foods. BMJ. 318; 581-584.
[147] Nordlee, J.A. et al. (1996). Identification of a Brazil-Nut Allergen in Transgenic Soybeans. N Engl J Med. 334; 688-692.
[148] Allen, A.H. (1996). Biotechnology: regulations may help consumer acceptance. Food Product Design. May, 80-85.
[149] Bindslev-Jensen, C. (2000). Genetically modified foods and allergenicity. Position Paper. European Academy for Allergology and Clinical Immunology.




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