Heterologous expression and biochemical characterisation of fourteen esterases from Helicoverpa armigera.

Esterases have recurrently been implicated in insecticide resistance in Helicoverpa armigera but little is known about the underlying molecular mechanisms. We used a baculovirus system to express 14 of 30 full-length esterase genes so far identified from midgut cDNA libraries of this species. All 14...

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Main Authors: Mark G Teese, Claire A Farnsworth, Yongqiang Li, Chris W Coppin, Alan L Devonshire, Colin Scott, Peter East, Robyn J Russell, John G Oakeshott
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3684599?pdf=render
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author Mark G Teese
Claire A Farnsworth
Yongqiang Li
Chris W Coppin
Alan L Devonshire
Colin Scott
Peter East
Robyn J Russell
John G Oakeshott
author_facet Mark G Teese
Claire A Farnsworth
Yongqiang Li
Chris W Coppin
Alan L Devonshire
Colin Scott
Peter East
Robyn J Russell
John G Oakeshott
author_sort Mark G Teese
collection DOAJ
description Esterases have recurrently been implicated in insecticide resistance in Helicoverpa armigera but little is known about the underlying molecular mechanisms. We used a baculovirus system to express 14 of 30 full-length esterase genes so far identified from midgut cDNA libraries of this species. All 14 produced esterase isozymes after native PAGE and the isozymes for seven of them migrated to two regions of the gel previously associated with both organophosphate and pyrethroid resistance in various strains. Thirteen of the enzymes obtained in sufficient yield for further analysis all showed tight binding to organophosphates and low but measurable organophosphate hydrolase activity. However there was no clear difference in activity between the isozymes from regions associated with resistance and those from elsewhere in the zymogram, or between eight of the isozymes from a phylogenetic clade previously associated with resistance in proteomic and quantitative rtPCR experiments and five others not so associated. By contrast, the enzymes differed markedly in their activities against nine pyrethroid isomers and the enzymes with highest activity for the most insecticidal isomers were from regions of the gel and, in some cases, the phylogeny that had previously been associated with pyrethroid resistance. Phospholipase treatment confirmed predictions from sequence analysis that three of the isozymes were GPI anchored. This unusual feature among carboxylesterases has previously been suggested to underpin an association that some authors have noted between esterases and resistance to the Cry1Ac toxin from Bacillus thuringiensis. However these three isozymes did not migrate to the zymogram region previously associated with Cry1Ac resistance.
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spelling doaj.art-c5ffe208d1d9451d8174eccb1e9372ee2022-12-21T21:09:36ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0186e6595110.1371/journal.pone.0065951Heterologous expression and biochemical characterisation of fourteen esterases from Helicoverpa armigera.Mark G TeeseClaire A FarnsworthYongqiang LiChris W CoppinAlan L DevonshireColin ScottPeter EastRobyn J RussellJohn G OakeshottEsterases have recurrently been implicated in insecticide resistance in Helicoverpa armigera but little is known about the underlying molecular mechanisms. We used a baculovirus system to express 14 of 30 full-length esterase genes so far identified from midgut cDNA libraries of this species. All 14 produced esterase isozymes after native PAGE and the isozymes for seven of them migrated to two regions of the gel previously associated with both organophosphate and pyrethroid resistance in various strains. Thirteen of the enzymes obtained in sufficient yield for further analysis all showed tight binding to organophosphates and low but measurable organophosphate hydrolase activity. However there was no clear difference in activity between the isozymes from regions associated with resistance and those from elsewhere in the zymogram, or between eight of the isozymes from a phylogenetic clade previously associated with resistance in proteomic and quantitative rtPCR experiments and five others not so associated. By contrast, the enzymes differed markedly in their activities against nine pyrethroid isomers and the enzymes with highest activity for the most insecticidal isomers were from regions of the gel and, in some cases, the phylogeny that had previously been associated with pyrethroid resistance. Phospholipase treatment confirmed predictions from sequence analysis that three of the isozymes were GPI anchored. This unusual feature among carboxylesterases has previously been suggested to underpin an association that some authors have noted between esterases and resistance to the Cry1Ac toxin from Bacillus thuringiensis. However these three isozymes did not migrate to the zymogram region previously associated with Cry1Ac resistance.http://europepmc.org/articles/PMC3684599?pdf=render
spellingShingle Mark G Teese
Claire A Farnsworth
Yongqiang Li
Chris W Coppin
Alan L Devonshire
Colin Scott
Peter East
Robyn J Russell
John G Oakeshott
Heterologous expression and biochemical characterisation of fourteen esterases from Helicoverpa armigera.
PLoS ONE
title Heterologous expression and biochemical characterisation of fourteen esterases from Helicoverpa armigera.
title_full Heterologous expression and biochemical characterisation of fourteen esterases from Helicoverpa armigera.
title_fullStr Heterologous expression and biochemical characterisation of fourteen esterases from Helicoverpa armigera.
title_full_unstemmed Heterologous expression and biochemical characterisation of fourteen esterases from Helicoverpa armigera.
title_short Heterologous expression and biochemical characterisation of fourteen esterases from Helicoverpa armigera.
title_sort heterologous expression and biochemical characterisation of fourteen esterases from helicoverpa armigera
url http://europepmc.org/articles/PMC3684599?pdf=render
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