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GMO Myths and Truths

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However, the authors of a 1990 study on the<br />

outbreak published in the New Engl<strong>and</strong> Journal<br />

of Medicine (NEJM) pointed out that blaming<br />

a failure in the carbon filtration process leaves<br />

unanswered the question of how the toxin got into<br />

the product in the first place. 72 This was a novel<br />

toxin that was not found in other companies’<br />

L-tryptophan products. The authors of the study,<br />

which was sponsored by the US Centers for<br />

Disease Control, noted that the new GM bacterial<br />

strain introduced by the manufacturer before the<br />

outbreak “may have produced larger quantities” of<br />

the toxin than earlier strains. 72<br />

One of the study’s co-authors, Dr Michael<br />

Osterholm, an epidemiologist at the Minnesota<br />

Department of Health, commented in a<br />

press article of August 1990 that the new<br />

bacterial strain “was cranked up to make more<br />

L-tryptophan <strong>and</strong> something went wrong. This<br />

obviously leads to that whole debate about genetic<br />

engineering.” 73<br />

Following Osterholm’s comment, a number<br />

of press articles appeared voicing doubts about<br />

the safety of genetic engineering. The FDA took<br />

on the role of exonerating genetic engineering<br />

from blame for the EMS epidemic. An article in<br />

Science magazine quoted FDA official Sam Page as<br />

saying that Osterholm was “propagating hysteria”.<br />

Tellingly, Page added, “The whole question: Is there<br />

any relation to genetic engineering? is premature<br />

– especially given the impact on the industry” 74 (our<br />

emphasis).<br />

Osterholm countered: “Anyone who looks<br />

at the data comes to the same conclusion [that<br />

there may be a link with genetic engineering]… I<br />

think FDA doesn’t want it to be so because of the<br />

implications for the agency.” 74<br />

James Maryanski, FDA biotech policy<br />

coordinator, blamed the EMS epidemic on Showa<br />

Denko’s changes to the purification process. 75<br />

Maryanski also said that genetic engineering could<br />

not have been solely or even chiefly responsible<br />

for EMS because cases of the illness had been<br />

reported for several years before Showa Denko<br />

introduced its genetically engineered bacterial<br />

Strain V in December 1988. 76<br />

However, a study published in 1994 shows that<br />

this argument is misleading. Showa Denko had<br />

named its bacterial strain “V” because there had<br />

been four previous strains of the bacterium. Over<br />

a period of years, Showa Denko had progressively<br />

introduced more genetic modifications into the<br />

bacteria used in its manufacturing process. It<br />

began using Strain V in December 1988, shortly<br />

before the EMS main outbreak in 1989. 69 But<br />

it had begun using its first genetically modified<br />

strain, Strain II, in 1984, according to lawyers<br />

who took on the cases of EMS sufferers. 77 This<br />

timescale means that Showa Denko’s genetically<br />

engineered bacteria could have been responsible<br />

for the EMS epidemic.<br />

The FDA responded to the crisis by claiming<br />

that all L-tryptophan was dangerous <strong>and</strong><br />

temporarily banning all L-tryptophan from sale. 78<br />

But a study sponsored by the Centers for Disease<br />

Control said if that were true, then “all tryptophan<br />

products of equal dose produced from different<br />

companies should have had the same [effect]”. The<br />

study concluded that this was not the case, since<br />

out of six manufacturers of L-tryptophan, only<br />

Showa Denko’s product was clearly associated with<br />

illness. 79<br />

If Showa Denko’s L-tryptophan were produced<br />

today, it would have to be assessed for safety, since<br />

it was derived from GM bacteria. However, since<br />

this L-tryptophan was greater than 99% pure <strong>and</strong><br />

devoid of DNA, it would be passed as substantially<br />

equivalent to the same substance obtained from<br />

non-GM organisms. In other words, the tests<br />

that would be required to detect novel toxins of<br />

this type would be seen as unnecessary <strong>and</strong> no<br />

labelling would be required. So the same tragedy<br />

would result. 80<br />

StarLink maize<br />

In 2000 in the US, people reported allergic<br />

reactions, some of them severe, to maize (corn)<br />

products. A GM Bt maize called StarLink was<br />

found to have contaminated the food supply.<br />

Regulators had allowed StarLink to be grown<br />

for animal feed <strong>and</strong> industrial use but had not<br />

approved it for human food because of suspicions<br />

that the Bt insecticidal protein it contained,<br />

known as Cry9C, might cause allergic reactions.<br />

The number of people who reported allergic<br />

reactions to maize products is not known because<br />

<strong>GMO</strong> <strong>Myths</strong> <strong>and</strong> <strong>Truths</strong> 49

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