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Gut Microbiota Mediate Insecticide Resistance in the Diamondback Moth, Plutella xylostella (L.)

The development of insecticide resistance in insect pests is a worldwide concern and elucidating the underlying mechanisms is critical for effective crop protection. Recent studies have indicated potential links between insect gut microbiota and insecticide resistance and these may apply to the diam...

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Autores principales: Xia, Xiaofeng, Sun, Botong, Gurr, Geoff M., Vasseur, Liette, Xue, Minqian, You, Minsheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5787075/
https://www.ncbi.nlm.nih.gov/pubmed/29410659
http://dx.doi.org/10.3389/fmicb.2018.00025
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author Xia, Xiaofeng
Sun, Botong
Gurr, Geoff M.
Vasseur, Liette
Xue, Minqian
You, Minsheng
author_facet Xia, Xiaofeng
Sun, Botong
Gurr, Geoff M.
Vasseur, Liette
Xue, Minqian
You, Minsheng
author_sort Xia, Xiaofeng
collection PubMed
description The development of insecticide resistance in insect pests is a worldwide concern and elucidating the underlying mechanisms is critical for effective crop protection. Recent studies have indicated potential links between insect gut microbiota and insecticide resistance and these may apply to the diamondback moth, Plutella xylostella (L.), a globally and economically important pest of cruciferous crops. We isolated Enterococcus sp. (Firmicutes), Enterobacter sp. (Proteobacteria), and Serratia sp. (Proteobacteria) from the guts of P. xylostella and analyzed the effects on, and underlying mechanisms of insecticide resistance. Enterococcus sp. enhanced resistance to the widely used insecticide, chlorpyrifos, in P. xylostella, while in contrast, Serratia sp. decreased resistance and Enterobacter sp. and all strains of heat-killed bacteria had no effect. Importantly, the direct degradation of chlorpyrifos in vitro was consistent among the three strains of bacteria. We found that Enterococcus sp., vitamin C, and acetylsalicylic acid enhanced insecticide resistance in P. xylostella and had similar effects on expression of P. xylostella antimicrobial peptides. Expression of cecropin was down-regulated by the two compounds, while gloverin was up-regulated. Bacteria that were not associated with insecticide resistance induced contrasting gene expression profiles to Enterococcus sp. and the compounds. Our studies confirmed that gut bacteria play an important role in P. xylostella insecticide resistance, but the main mechanism is not direct detoxification of insecticides by gut bacteria. We also suggest that the influence of gut bacteria on insecticide resistance may depend on effects on the immune system. Our work advances understanding of the evolution of insecticide resistance in this key pest and highlights directions for research into insecticide resistance in other insect pest species.
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spelling pubmed-57870752018-02-06 Gut Microbiota Mediate Insecticide Resistance in the Diamondback Moth, Plutella xylostella (L.) Xia, Xiaofeng Sun, Botong Gurr, Geoff M. Vasseur, Liette Xue, Minqian You, Minsheng Front Microbiol Microbiology The development of insecticide resistance in insect pests is a worldwide concern and elucidating the underlying mechanisms is critical for effective crop protection. Recent studies have indicated potential links between insect gut microbiota and insecticide resistance and these may apply to the diamondback moth, Plutella xylostella (L.), a globally and economically important pest of cruciferous crops. We isolated Enterococcus sp. (Firmicutes), Enterobacter sp. (Proteobacteria), and Serratia sp. (Proteobacteria) from the guts of P. xylostella and analyzed the effects on, and underlying mechanisms of insecticide resistance. Enterococcus sp. enhanced resistance to the widely used insecticide, chlorpyrifos, in P. xylostella, while in contrast, Serratia sp. decreased resistance and Enterobacter sp. and all strains of heat-killed bacteria had no effect. Importantly, the direct degradation of chlorpyrifos in vitro was consistent among the three strains of bacteria. We found that Enterococcus sp., vitamin C, and acetylsalicylic acid enhanced insecticide resistance in P. xylostella and had similar effects on expression of P. xylostella antimicrobial peptides. Expression of cecropin was down-regulated by the two compounds, while gloverin was up-regulated. Bacteria that were not associated with insecticide resistance induced contrasting gene expression profiles to Enterococcus sp. and the compounds. Our studies confirmed that gut bacteria play an important role in P. xylostella insecticide resistance, but the main mechanism is not direct detoxification of insecticides by gut bacteria. We also suggest that the influence of gut bacteria on insecticide resistance may depend on effects on the immune system. Our work advances understanding of the evolution of insecticide resistance in this key pest and highlights directions for research into insecticide resistance in other insect pest species. Frontiers Media S.A. 2018-01-23 /pmc/articles/PMC5787075/ /pubmed/29410659 http://dx.doi.org/10.3389/fmicb.2018.00025 Text en Copyright © 2018 Xia, Sun, Gurr, Vasseur, Xue and You. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Xia, Xiaofeng
Sun, Botong
Gurr, Geoff M.
Vasseur, Liette
Xue, Minqian
You, Minsheng
Gut Microbiota Mediate Insecticide Resistance in the Diamondback Moth, Plutella xylostella (L.)
title Gut Microbiota Mediate Insecticide Resistance in the Diamondback Moth, Plutella xylostella (L.)
title_full Gut Microbiota Mediate Insecticide Resistance in the Diamondback Moth, Plutella xylostella (L.)
title_fullStr Gut Microbiota Mediate Insecticide Resistance in the Diamondback Moth, Plutella xylostella (L.)
title_full_unstemmed Gut Microbiota Mediate Insecticide Resistance in the Diamondback Moth, Plutella xylostella (L.)
title_short Gut Microbiota Mediate Insecticide Resistance in the Diamondback Moth, Plutella xylostella (L.)
title_sort gut microbiota mediate insecticide resistance in the diamondback moth, plutella xylostella (l.)
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5787075/
https://www.ncbi.nlm.nih.gov/pubmed/29410659
http://dx.doi.org/10.3389/fmicb.2018.00025
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