The fate of recombinant DNA in fallow deer
(Dama dama) was investigated by feeding a diet of
isogenic or genetically modified (GM) maize expressing
Cry1Ab protein against the European corn borer (Ostrinia
nubilalis). To study the degradability of ingested DNA, fragments were detectable in contents of rumen, abomasums,
jejunum, caecum and colon and occasionally in
visceral tissues. In contrast, no fragments of the recombinant
cry1Ab gene were detectable in gastrointestinal (GI)
contents. The Cry1Ab protein was analysed using an
enzyme-linked immunosorbent assay (ELISA) and immunoblotting
technique. Neither ELISA nor immunoblotting
yielded positive signals of immunoactive Cry1Ab protein in
GI contents and tissues of fallow deer fed with GM maize.
In conclusion, after uptake of GM maize, neither cry1Abspecific
gene fragments nor Cry1Ab protein were detected
in the GI tract of fallow deer, indicating complete digestion
of the GM maize. Additional investigations on the
germination capacity of conventional rapeseed and maize
seed after ingestion by fallow deer and faecal excretion
(endozoochory) were performed to draw conclusions
regarding a potential spreading of germinable GM crop
seed by deer. Germination tests revealed that germinable
rapeseed kernels were detectable in faeces; in contrast, no
intact maize seeds were found in faeces.
polymerase chain reaction (PCR) assays were introduced to
detect fragments of the endogenous, highly abundant
chloroplast-specific rubisco gene, the maize-specific zein
gene and the recombinant cry1Ab gene. PCR analysis
revealed that small chloroplast- and maize-specific DNA
«The fate of recombinant DNA in fallow deer
(Dama dama) was investigated by feeding a diet of
isogenic or genetically modified (GM) maize expressing
Cry1Ab protein against the European corn borer (Ostrinia
nubilalis). To study the degradability of ingested DNA, fragments were detectable in contents of rumen, abomasums,
jejunum, caecum and colon and occasionally in
visceral tissues. In contrast, no fragments of the recombinant
cry1Ab gene were detectable in gastrointestinal (GI)
contents....
»