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Toxicological, Biochemical, and Histopathological Analyses Demonstrating That Cry1C and Cry2A Are Not Toxic to Larvae of the Honeybee, Apis mellifera.
Wang, Yuan-Yuan; Li, Yun-He; Huang, Zachary Y; Chen, Xiu-Ping; Romeis, Jörg; Dai, Ping-Li; Peng, Yu-Fa.
Affiliation
  • Wang YY; †State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, No. 2 West Yuanmingyuan Road, Haidian District, Beijing, People's Republic of China.
  • Li YH; †State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, No. 2 West Yuanmingyuan Road, Haidian District, Beijing, People's Republic of China.
  • Huang ZY; ‡Department of Entomology, Michigan State University, East Lansing, Michigan, United States.
  • Chen XP; †State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, No. 2 West Yuanmingyuan Road, Haidian District, Beijing, People's Republic of China.
  • Romeis J; †State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, No. 2 West Yuanmingyuan Road, Haidian District, Beijing, People's Republic of China.
  • Dai PL; §Agroscope, Institute for Sustainability Sciences ISS, 8046 Zurich, Switzerland.
  • Peng YF; ∥Key Laboratory of Pollinating Insect Biology of Ministry of Agriculture, Institute of Apicultural Research, Chinese Academy of Agricultural Science, Beijing 100093, People's Republic of China.
J Agric Food Chem ; 63(27): 6126-32, 2015 Jul 15.
Article in En | MEDLINE | ID: mdl-26084400
The honey bee, Apis mellifera, is commonly used as a test species for the regulatory risk assessment of insect-resistant genetically engineered (IRGE) plants. In the current study, a dietary exposure assay was developed, validated, and used to assess the potential toxicity of Cry1C and Cry2A proteins from Bacillus thuringiensis (Bt) to A. mellifera larvae; Cry1C and Cry2A are produced by different IRGE crops. The assay, which uses the soybean trypsin inhibitor (SBTI) as a positive control and bovine serum albumin (BSA) as a negative control, was used to measure the responses of A. mellifera larvae to high concentrations of Cry1C and Cry2A. Survival was reduced and development was delayed when larvae were fed SBTI (1 mg/g diet) but were unaffected when larvae were fed BSA (400 µg/g), Cry1C (50 µg/g), or Cry2A (400 µg/g). The enzymatic activities of A. mellifera larvae were not altered and their midgut brush border membranes (BBMs) were not damaged after being fed with diets containing BSA, Cry1C, or Cry2A; however, enzymatic activities were increased and BBMs were damaged when diets contained SBTI. The study confirms that Cry1C and Cry2A have no acute toxicity to A. mellifera larvae at concentrations >10 times higher than those detected in pollen from Bt plants.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bacterial Proteins / Bees / Endotoxins / Hemolysin Proteins / Larva Type of study: Risk_factors_studies Limits: Animals Language: En Journal: J Agric Food Chem Year: 2015 Document type: Article Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bacterial Proteins / Bees / Endotoxins / Hemolysin Proteins / Larva Type of study: Risk_factors_studies Limits: Animals Language: En Journal: J Agric Food Chem Year: 2015 Document type: Article Country of publication: