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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,
Jazyk angličtina Země Velká Británie
Typ dokumentu časopisecké články
NLK
Free Medical Journals
od 1997 do Před 1 rokem
Freely Accessible Science Journals
od 2004 do Před 1 rokem
PubMed Central
od 1997 do Před 1 rokem
Europe PubMed Central
od 1997 do Před 1 rokem
Open Access Digital Library
od 1905-04-22
Open Access Digital Library
od 1997-01-01
PubMed
28724730
DOI
10.1098/rspb.2017.0440
Knihovny.cz E-zdroje
- MeSH
- Bacillus thuringiensis MeSH
- bakteriální proteiny genetika MeSH
- členovci * MeSH
- endotoxiny genetika MeSH
- geneticky modifikované rostliny genetika MeSH
- hemolyziny genetika MeSH
- kukuřice setá genetika MeSH
- larva MeSH
- potravní řetězec * MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
- Publikační typ
- časopisecké články 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.
Citace poskytuje 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 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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