Michael Balter wrote:
February will mark the 33rd
anniversary of the Asilomar conference on what we used to call
recombinant DNA
still
do - indeed one of the few low-emotion tags left for
it
...
a session on recombinant DNA and
genetic engineering might attract a lot of people if it were properly
publicized
I can
assure you that the world leaders Beckwith et al were extremely
visible from the S. Pacific in that mid-1970s early scepticism about
GM. Some of us would probably be able to get to the session
Michael proposes, which would be partly for the purpose of honouring
those pioneer critics.
Meanwhile, I comment on Michael's assessment of what has
happened since.
...
the work went ahead albeit with
containment safeguards that ultimately defused public
concern;
yes
they did - but wrongfully. Release of GMOs, especially GM-crops
in a few countries, has dominated the concerns over the past decade,
almost to the exclusion of the concerns about some extremely dangerous
GMOs which are admitted to require containment - in the
hands of people who mostly think concerns about hazards from GMOs are
absurd. Even the extremely biased pro-GM Eichelbaum Commission
in my country recommended a review of the containment rules.
that the more serious dangers we
warned about have not actually come to pass, eg epidemics of
genetically modified microbes;
How do you
know? Who has been looking?
that the basic techniques of
genetic engineering have formed the basis of much or even most of the
advances in biology over the past 30 years;
I
consider that a biased exaggeration. If what Michael says is
true, or at least a reasonable opinion, we should be able to read
reviews summarising it. Where can we read a review or two
about advances in biology from GM?
but that the technology has also
fallen into the hands of major corporations such as Monsanto et al
such that concerns over GMOs and their regulation continue to be in
the forefront; and that the ethical issues related to genetic
engineering are still very much with us.
That is
for sure.
I
cannot think of a more suitable topic for a session at, or next to,
the AAAS mtg in Boston. One contribution could be the truth
about the EMS disaster (which leading jnls refuse to publish) -
here's a summary.
THE THALIDOMIDE OF GENETIC
'ENGINEERING'
L R
B Mann, D Straton & W E Crist
By the end of the 1980s some millions of people, mostly in North
America, were supplementing their diet with L-tryptophan, an essential
amino-acid present in proteins of any normal diet. Amino-acids
such as tryptophan are routinely produced in micro-breweries using
suitable microbial cultures. One producer, Showa Denko K.K.,
artificially inserted genes into a bacterial species to increase its
production of tryptophan.
Then in late 1989, some 5,000 - 10,000 in North America fell ill with
a highly unusual illness, EMS (eosinophilia-myalgia syndrome), caused
by Showa Denko tryptophan. Within months, dozens had been killed
by EMS and thousands maimed. Today thousands continue to suffer
permanent nasty effects, and a trickle of them continue to die early
(totalling at least 80 by now in the USA). The epidemic ceased
when over-the-counter tryptophan was severely restricted.
Two cases were reported in Australia, and one in New Zealand.
The tryptophan those patients took was not traced to manufacturer.
The total killed is not exactly known but may be in the region of a
few hundred. Showa Denko has paid around US$2,000,000,000 to
avoid damages trials.
We emphasize that if thalidomide had happened to cause a
type of birth defect that was already common, e.g. cleft palate
or severe mental retardation, we would still not know about the harm,
and pregnant women would have kept on taking it for its undoubted
benefits. The fractional addition to figures that were already
relatively large would not have been statistically significant.
But as it turned out, the damage noticed was of a kind that most
doctors never see in a whole career - drastic malformations of the
arms & legs - so although the numbers were not huge these cases
were picked up.
Similarly, impurities in Showa Denko's genetically 'engineered'
(GE) tryptophan happened to cause an illness - EMS - which was novel.
The surge of numbers therefore stood out and got noticed. If
SDKK's poison had caused the same numbers of a common illness instead,
say asthma, we would still not know about it. Or if it had
caused delayed harm, such as cancer 20 - 30 years later, or senile
dementia in some whose mothers had taken it early in pregnancy, there
would have been no way to attribute the harm to the cause.
This reminds us of the need for extreme caution with GE foods.
They must be assumed guilty until thorough tests have suggested they
are, if not innocent, at worst guilty of only minor dangers.
Such is nowhere near the case today as large companies rush to market
their GE foods.
It is very disappointing to find a leading physician writing on behalf
of the RSNZ about this disaster thus: "Rare cases of EMS were
known before the introduction of the genetically engineered bacterium,
which further supports the hypothesis that EMS is not due to the
genetic engineering event." An exact analogue of that
argument would run: "Rare cases of seal-limb were known before
the introduction of thalidomide, which further supports the hypothesis
that seal-limb is not due to thalidomide."
But even more important is the fact that the trickle of about 100
early EMS cases, years before the epidemic of late 1989, were due to
(early versions of) Showa Denko GE bacterial cultures.
None of the half-dozen other manufacturers' tryptophan caused EMS.
No other manufacturer used gene-splicing to produce
tryptophan.
The contrast is startling with the elaborate procedure before
registration of a new drug. It has taken a decade to get legal
approval for supplementing humans with (a modified version of) the
human hormone amylin, for treating diabetics. Yet GE foods are
urged for legal distribution in great haste and with only extremely
scanty testing, and the main discussion so far has been whether they
should be labelled.
Labelling would not in itself be wrong, but can of course not
substitute for the careful lengthy testing that would be needed before
any GE food should be approved for human consumption. Labelling
of GE food would imply acceptance by authorities, as does the
ingredient list of any labelled food.
The Showa Denko disaster is crucial to understanding GE food. If
a purified single chemical - the natural amino-acid
L-tryptophan, better than 99% pure and definitely satisfying the
notorious 'substantial equivalence' test - can turn out
when GE'd to kill a hundred or so and cripple thousands, what will it
take to check properly a potato expressing a synthetic 'exact' copy of
a gene for a toxin from the African clawed toad?
And most urgently, the attempt to count purified amino-acids, sugars,
oils etc. as 'substantially equivalent' is shown by the Showa Denko
disaster to be a gamble. The assumption that soy oil from GE
soybeans is exactly equivalent to ordinary soy oil requires the most
careful scientific measurements to check it. Merely assuming
'substantial equivalence' will not do.
Those who search the Internet on this topic will soon discover the
claim by apologists for GE that the problem was only decreased
purification of tryptophan. We disagree for several reasons -
mainly, the first three GE strains had been causing EMS (about 100
cases) for years before this slackening of purification procedure in
Jan 1989 when also the 'superproducer' strain went into production and
caused the epidemic. But this question cannot be settled with
finality unless Showa Denko releases the GE microbes for detailed
examination.
Whether you believe the impurities were due to incompetent
purification & monitoring, or to deviant metabolism in the
GE-bugs, or both, you had better believe that the fabled
'substantially equivalent' assumption flopped in that epidemic of
crippling and lethal illness.
Although GE proponents claim that the EMS epidemic was caused solely
by faulty filtering, it is possible to question their seriousness.
None of them has publicly argued that the Health Food supplement
industry should be subject to legal controls for purity & efficacy
comparable to those applied to the pharmaceutical industry; yet this
would be logical if indeed such a deadly epidemic occurred solely as a
result of inadequate purification in manufacturing.
Either way, biotechnology - which includes GE but also
includes other processes such as purifying the mixture "lyprinol"
from mussels - requires much-enhanced scrutiny.
Main sources
1. L-Tryptophan Puzzle Takes New Twist, Science 249,
988, 31 August 1990
2. Does Medical Mystery Threaten Biotech? Science
250, 619, 2 November 1990
3. EMS and Tryptophan Production: A Cautionary Tale,
Trends in Biotech 12 : 346-352, Sept 1994
4. Eosinophilia-myalgia syndrome. Results of national
surveillance, J Am Med Assoc 264: 1698-703 1990
5. Tryptophan produced by Showa Denko and epidemic
eosinophilia-myalgia syndrome.
J Rheumatol 46 Suppl 1996.
81-91.
6. Toxic L-tryptophan: Shedding Light on a Mysterious Epidemic.
by William E. Crist.
http://www.seedsofdeception.com/Public/Ltryptophan/1Introduction/inde
x.cfm
Dr Mann <
[log in to unmask]>, a biochemist, served for its first
dozen years on the Toxic Substances Board advising successive New
Zealand Ministers of Health on poisons.
Dr Straton is a psychiatrist who has taken a special interest in
therapeutic uses of tryptophan.
Mr Crist is a publicist who has interviewed researchers, victims, and
lawyers involved with EMS.
This article is available at
http://www.connectotel.com/gmfood/trypto.html. It is updated
from Soil & Health Aug 1999.