'Bt' toxins are a favourite tool of
genetic engineers for creating crops which generate their own
pesticide to kill whatever is their most troublesome insect pest.
In Nature, such toxins are formed by a
variety of strains of Bacillus thuringienses
bacteria (hence 'Bt') found in soil and on plants. Organic farmers
may use Bacillus thrunigienses
fermentations as natural, short-lived insecticide sprays on their
crops. Outside of organic agriculture however, Bt-toxin containing
formula are used to control specific problematic insects, such as
disease-carrying mosquitoes.
Bt toxins are proteins which are active in the conditions found in insect guts, and which bind to substances on the insect-gut surface causing damage there which quickly leads to death.
In this model view
of 'Bt' toxins, they are inactive in the guts of other, non-target
animals, easily digested in the acid-conditions in the mammalian
stomach, and will only kill specific insects whose gut-lining has the
specific binding sites for the specific variety of Bt they have
eaten. This makes Bt very safe for humans and other wildlife in the
environment.
Or does it? The
model is being questioned with regard to whether it's the whole story
[1], and in particular, whether Bt proteins are as specific to
insects as advertised.
A study published
in 2015 noted that "The effects of Bti* on amphibians have
received little attention" and that "the tests used to
justify the approval for use and release of Bt products into the
market as well as the protocols used to assess its toxicity are
extremely superficial".
Amphibians such as
frogs are sensitive to toxins and are commonly used as biomarkers for
environmental health; they also lay eggs in stagant water where the
tadpoles live until the adult frogs develop. As every gardener
knows, frogs are important in pest control, and are to be encouraged.
Tadpoles and mosquito larvae share the same environmental niche.
And the conditions in their guts aren't so different either.
Besides
the question of the Bt protein itself, environmental treatments use
commercial formulations. While the toxin
is thoroughly tested to make sure it kills the required pest (such as
a specific species of mosquito), the formulations will
include agents considered to be 'inert' and are commercially
confidential, so receive no further attention. 'Inerts' are included
to disperse the Bt in water, stick it to the insect's food, and to
help the toxin to kill. All of these properties are potentially
harmful to life in their own right.
Awareness of some
major holes in the science and in the gaps in the grounds for Bt
safety claims, scientists in Argentina treated tadpoles with a common
Bt formulation and measured a range of health effects.
The tadpoles were
exposed to the Bt formula for two days (the usual life-span of Bt in
the environment) at the range of concentrations used in practice.
At the highest
concentration, all the tadpoles died and no further tests could be
carried out.
At lower
concentrations of Bt, mortality was dose-related. Because stagnant
water will be re-treated at regular intervals, the total deaths of
tadpoles in a real-life situations are therefore likely to be
significant.
Biochemical markers
for stress were elevated in tadpoles exposed to higher concentrations
of Bt.
Increased
structural abnormalities of the cell nucleus (this contains
the DNA and genes) were evident
in Bt-treated tadpoles. This kind of toxicity isn't dose-related
because the defects arise during cell-division, when new nuclei are
formed, and won't occur if the toxin is acting to suppress
cell-division.
Note
that standard gene toxicity testing tends to use bacteria
whose DNA/nuclear structure is fundamentally different from animals.
Finally, the
Argentinean scientists looked at the tadpole's guts, revealing gross
tissue changes in the gut wall and its blood supply, and even erosion
of the gut-lining, indicative of inflammation and stressor-defences.
OUR COMMENT
In deprived urban
areas in Argentina, waterbodies are mass-treated with Bt and some are
then consumed by people. Although simulated digestion studies
demonstrated total Bt degradation in the human digestive system, Bt
proteins have been found circulating in Canadian women and their
unborn babies. This was unexpected and has been attributed to the
consumption of Bt-generating GM maize. Worryingly, it means our
concept of Bt digestability is way out. It may also mean that
exposure to 'inerts' is giving a helping hand to Bt and a whole raft
of other environmental toxins into our bodies.
Bt in GM dust and
organic applications (where there's no digestion and are no 'inerts')
has been reported to cause allergic respiratory problems in farm
workers.
Ask yourself is Bt
protein outside of bacteria and stabilised in GM food safe to eat?
Is Bt protein stabilised in insecticidal formulations safe to drink?
You may by now have a gut feeling they're not.
Background
*Bti refers to a strain of Bacillus thrunigienses called 'israelensis' which is used in stagnant water where mosquitoes lay their eggs.
SOURCES:
- Rafael C. Lajmanovich, et al., 2015, Toxicity of Bacillus thuringiensis var. israelensis in aqueous suspension on the South American common frog Leptodactylus latrans (Anura: Leptodactylidae) tadpoles, Environmental Research 136
- Dr. Eva Sirinathsinghji, Commercial Formulations of Bt Toxins Lethal to Amphibians, Institute of Science in Society Report, 14.01.16Photo credit: Tadpoles. By Geoff Gallice from Gainesville, FL, USA (Treefrog tadpoles) [CC BY 2.0 (http://creativecommons.org/licenses/by/2.0)], via Wikimedia Commons
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