May 2013
'MON810' insecticidal maize
is the only major GM feed crop permitted for cultivation in Europe.
However, eight European
countries have banned it, and recently, Italy has moved this a stage
further and asked the European Commission to withdraw its approval
for the crop.
The scientific and anecdotal
evidence of problems in livestock fed MON810 and other 'Bt' crops is
mounting but fragmented and inconsistent. Over a dozen feeding
studies measuring various parameters in various animals given various
Bt-based feeds have been published. All have found
physiological changes in the animals. Some of the results support
each other, others do not, and all are short-term. More than
anything else, they highlight the gaps: there's an absence of
long-term experiments; there's a lack of in-depth physiological
studies, especially of intestinal and immune responses. Most of all,
it's clear that no one knows what to look for: there's an urgent need
to identify key biomarkers for Bt-maize-linked symptoms
The latest feeding study to
be published has shed at least some new light on the biomarker
question. It involved a very detailed look at salmon fed GM maize
for periods of 1 and 3 months.
Farmed salmon are commonly
feed maize 'gluten meal' which is a mildly treated protein extract of
the kernels. Any transgenic or unexpected protein by-products in
such feed should be concentrated and largely intact. Previous
studies suggest that the MON810 Bt protein itself would survive this
processing partially intact: it would retain its pore-forming ability
which kills cells by damaging their outer membrane, but it's ability
to latch on to target cells would be impaired.
Besides comparing MON 810
maize with its closest relative (near isogenic counterpart), the
scientists tested what happened when the fish were sensitised by the
inclusion of soya meal which induces symptoms similar to Irritable
Bowel Syndrome (IBS) in humans.
They looked at a wide range
of physiological responses including growth, digestive function,
basic health parameters (blood cells and chemistry, organs), immune
reactions and stress.
No differences were found in
the growth and blood parameters (COMMENT Note that these are the
main health biomarkers routinely used in feeding 'safety' trials).
However, this more detailed investigation found changes in nutrient
metabolism, such as reduced lipid stores and impaired mineral
digestion, suggesting the the fish were unable to use the GM feed as
efficiently as conventional maize.
Inclusion
of the soya sensitiser, induced localised intestinal immune responses
and potentiated inflammation. (COMMENT Note that Bt
toxins which are less processed and so retain all their
toxin-promoting potential could be much more harmful)
The
authors noted that their findings differed from those in a 2007 paper
on the same animal fed the same GM maize event: the previous study
found reduced growth and increased organ weight, but no change in
nutrient metabolism. This suggests these particular parameters,
which are the ones routinely relied on to assess feeding quality and
have been extrapolated into 'safety' studies, are too insensitive to
use for the latter. The development of gut-cell proliferation tests
appears to offer a more reliable biomarker for Bt effects.
OUR COMMENT
Since
maintenance of the gut requires as much as 20-25% of nutrient energy
requirements, adverse cell reactions could certainly be debilitating.
Add to this that 5-11% of the population of most countries suffer
from IBS, and many more cases probably go unreported: such people
could well be hyper-sensitive to the effects of Bt maize.
None of
the Bt feeding studies have given MON 810 a clean bill of health, but
few are pointing in exactly the same direction. Something's wrong,
but what?
The
authors of the latest publication seem to be the first one to raise
the issue of “other antigens” which might be present in GM feed
besides the Bt protein and could produce side-effects.
This is
a key point, especially in light of the variations in physiological
changes found in different experiments. Such “other antigens”
could be emerging in the Bt-plant physiology in response to varying
environmental influences or agronomic regimes.
It's
worth remembering Arpad Pusztai in Aberdeen, who was commissioned to
develop safety testing for GM foods back in the 1990s. Dr Pusztai
also homed in on adverse reactions in the intestinal cells: his
success in finding them triggered the first of many orchestrated
defamatory attacks on scientists who dared to publish GM-unfriendly
results.
Perhaps
its time we insisted that regulators revisit the type of tests of
harm Dr. Pusztai was working on, and develop the sort of biomarkers
highlighted by this Bt-feeding study.
SOURCES:
- Jinni Gu et al., 2013, Effects of oral Bt-maize (MON810) exposure on growth and health parameters in normal and sensitised Atlantic salmon, Salmo salar L., British Journal of Nutrition, 109
- R. Spiller et al., 2007, Guidelines on the irritable bowel syndrome: mechanisms and practical management, Gut 56
- IBS - Epidemiology, www.patient.co.uk/doctor/irritable-bowel-syndrome, April 2013
- Italy asks EU to halt GM maize cultivation, http://phys.org/news, 4.04.13
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