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Stacked Bt maize and arthropod predators: exposure to insecticidal Cry proteins and potential hazards
Z. Svobodová, Y. Shu, O. Skoková Habuštová, J. Romeis, M. Meissle,
Language English Country Great Britain
Document type Journal Article
NLK
Free Medical Journals
from 1997 to 1 year ago
Freely Accessible Science Journals
from 2004 to 1 year ago
PubMed Central
from 1997 to 1 year ago
Europe PubMed Central
from 1997 to 1 year ago
Open Access Digital Library
from 1905-04-22
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from 1997-01-01
- MeSH
- Bacillus thuringiensis MeSH
- Bacterial Proteins genetics MeSH
- Arthropods * MeSH
- Endotoxins genetics MeSH
- Plants, Genetically Modified genetics MeSH
- Hemolysin Proteins genetics MeSH
- Zea mays genetics MeSH
- Larva MeSH
- Food Chain * MeSH
- Animals MeSH
- Check Tag
- Animals MeSH
- Publication type
- Journal Article MeSH
Genetically engineered (GE) crops with stacked insecticidal traits expose arthropods to multiple Cry proteins fromBacillus thuringiensis(Bt). One concern is that the different Cry proteins may interact and lead to unexpected adverse effects on non-target species. Bi- and tri-trophic experiments with SmartStax maize, herbivorous spider mites (Tetranychus urticae), aphids (Rhopalosiphum padi), predatory spiders (Phylloneta impressa), ladybeetles (Harmonia axyridis) and lacewings (Chrysoperla carnea) were conducted. Cry1A.105, Cry1F, Cry3Bb1 and Cry34Ab1 moved in a similar pattern through the arthropod food chain. By contrast, Cry2Ab2 had highest concentrations in maize leaves, but lowest in pollen, and lowest acquisition rates by herbivores and predators. While spider mites contained Cry protein concentrations exceeding the values in leaves (except Cry2Ab2), aphids contained only traces of some Cry protein. Predators contained lower concentrations than their food. Among the different predators, ladybeetle larvae showed higher concentrations than lacewing larvae and juvenile spiders. Acute effects of SmartStax maize on predator survival, development and weight were not observed. The study thus provides evidence that the different Cry proteins do not interact in a way that poses a risk to the investigated non-target species under controlled laboratory conditions.
References provided by Crossref.org
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- $a Svobodová, Zdeňka $u Agroscope, Research Division Agroecology and Environment, Reckenholzstrasse 191, Zurich 8046, Switzerland. Institute of Ecology and Evolution, University of Bern, Baltzerstrasse 6, Bern 3012, Switzerland. Institute of Entomology, Biology Centre CAS, Branišovská 31, České Budějovice 37005, Czech Republic. Faculty of Science, University of South Bohemia, Branišovská 31, České Budějovice 37005, Czech Republic.
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- $a Stacked Bt maize and arthropod predators: exposure to insecticidal Cry proteins and potential hazards / $c Z. Svobodová, Y. Shu, O. Skoková Habuštová, J. Romeis, M. Meissle,
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- $a Genetically engineered (GE) crops with stacked insecticidal traits expose arthropods to multiple Cry proteins fromBacillus thuringiensis(Bt). One concern is that the different Cry proteins may interact and lead to unexpected adverse effects on non-target species. Bi- and tri-trophic experiments with SmartStax maize, herbivorous spider mites (Tetranychus urticae), aphids (Rhopalosiphum padi), predatory spiders (Phylloneta impressa), ladybeetles (Harmonia axyridis) and lacewings (Chrysoperla carnea) were conducted. Cry1A.105, Cry1F, Cry3Bb1 and Cry34Ab1 moved in a similar pattern through the arthropod food chain. By contrast, Cry2Ab2 had highest concentrations in maize leaves, but lowest in pollen, and lowest acquisition rates by herbivores and predators. While spider mites contained Cry protein concentrations exceeding the values in leaves (except Cry2Ab2), aphids contained only traces of some Cry protein. Predators contained lower concentrations than their food. Among the different predators, ladybeetle larvae showed higher concentrations than lacewing larvae and juvenile spiders. Acute effects of SmartStax maize on predator survival, development and weight were not observed. The study thus provides evidence that the different Cry proteins do not interact in a way that poses a risk to the investigated non-target species under controlled laboratory conditions.
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