![]() |
|
|
Centre for Plant Sciences, University of Leeds, Leeds, LS2 9JT, UK and * BIBRA International, Carshalton, Surrey, SM5 4DS, UK
2To whom correspondence should be addressed. E-mail: h.j.atkinson{at}leeds.ac.uk.
A protein-engineered rice cystatin (OcI
D86) provides transgenic, partial crop resistance to plant nematodes. This study determined whether its oral uptake has adverse effects on male Sprague-Dawley rats when they are administered by oral gavage 0.110 mg OcI
D86/kg body weight daily for 28 d. Body weight and water and food intakes were unaltered for most of the study. The only significant changes in fresh weight of nine organs were for the liver (4% decrease; P < 0.05) and the empty cecum (14% increase; P < 0.05) at the two lowest doses and the highest dose of OcI
D86, respectively. No abnormalities in either organ were detected by histochemistry. There were no changes in the urine or in hematological variables measured, and blood serum revealed no dose-dependent responses for any of 17 variables measured. OcI
D86 was degraded by boiling with a 50% loss of its inhibition of papain after 9.2 ± 8.0 min. It also showed >95% loss of such inhibition after 15 s in simulated gastric fluid. The results suggest that the no effect level (NOEL) for OcI
D86 is >10 mg/(kg · d). This provides a range of dietary exposure >2002000 fold depending upon the promoter used to control its expression in potato.
KEY WORDS: toxicity cystatin OcI
D86 anti-nematode biopesticide