dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-27T11:28:18Z
dc.date.accessioned2022-10-05T18:43:02Z
dc.date.available2014-05-27T11:28:18Z
dc.date.available2022-10-05T18:43:02Z
dc.date.created2014-05-27T11:28:18Z
dc.date.issued2013-02-01
dc.identifierJournal of Invertebrate Pathology, v. 112, n. 2, p. 152-158, 2013.
dc.identifier0022-2011
dc.identifier1096-0805
dc.identifierhttp://hdl.handle.net/11449/74473
dc.identifier10.1016/j.jip.2012.11.011
dc.identifierWOS:000314381000009
dc.identifier2-s2.0-84871595010
dc.identifier2-s2.0-84871595010.pdf
dc.identifier1458288287757880
dc.identifier1295051340591836
dc.identifier7179273060624761
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3923429
dc.description.abstractThe polyphagous pests belonging to the genus Spodoptera are considered to be among the most important causes of damage and are widely distributed throughout the Americas'. Due to the extensive use of genetically modified plants containing Bacillus thuringiensis genes that code for insecticidal proteins, resistant insects may arise. To prevent the development of resistance, pyramided plants, which express multiple insecticidal proteins that act through distinct mode of actions, can be used. This study analyzed the mechanisms of action for the proteins Cry1Ia10 and Vip3Aa on neonatal Spodoptera frugiperda, Spodoptera albula, Spodoptera eridania and Spodoptera cosmioides larvae. The interactions of these toxins with receptors on the intestinal epithelial membrane were also analyzed by binding biotinylated toxins to brush border membrane vesicles (BBMVs) from the intestines of these insects. A putative receptor of approximately 65. kDa was found by ligand blotting in all of these species. In vitro competition assays using biotinylated proteins have indicated that Vip3Aa and Cry1Ia10 do not compete for the same receptor for S. frugiperda, S. albula and S. cosmioides and that Vip3Aa was more efficient than Cry1Ia10 when tested individually, by bioassays. A synergistic effect of the toxins in S. frugiperda, S. albula and S. cosmioides was observed when they were combined. However, in S. eridania, Cry1Ia10 and Vip3Aa might compete for the same receptor and through bioassays Cry1Ia10 was more efficient than Vip3Aa and showed an antagonistic effect when the proteins were combined. These results suggest that using these genes to develop pyramided plants may not prove effective in preventing the development of resistance in S. eridiana. © 2012 Elsevier Inc.
dc.languageeng
dc.relationJournal of Invertebrate Pathology
dc.relation2.511
dc.relation0,929
dc.relation0,929
dc.rightsAcesso aberto
dc.sourceScopus
dc.subjectIn vitro competition assays
dc.subjectReceptor binding
dc.subjectSpodoptera albula
dc.subjectSpodoptera cosmioides
dc.subjectSpodoptera eridania
dc.subjectSpodoptera frugiperda
dc.subjectBacillus thuringiensis
dc.subjectHexapoda
dc.subjectLepidoptera
dc.subjectSpodoptera
dc.titleBacillus thuringiensis Cry1Ia10 and Vip3Aa protein interactions and their toxicity in Spodoptera spp. (Lepidoptera)
dc.typeArtigo


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