Enhanced capacity of a leaf beetle to combat dual stress from entomopathogens and herbicides mediated by associated microbiota
Herbicides have demonstrated their impact on insect fitness by affecting their associated microbiota or altering the virulence of entomopathogenic fungi toward insects. However, limited research has explored the implications of herbicide stress on the intricate tripartite interaction among insects,...
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Veröffentlicht in: | Integrative zoology 2024-11, Vol.19 (6), p.1092-1104 |
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description | Herbicides have demonstrated their impact on insect fitness by affecting their associated microbiota or altering the virulence of entomopathogenic fungi toward insects. However, limited research has explored the implications of herbicide stress on the intricate tripartite interaction among insects, associated bacterial communities, and entomopathogens. In this study, we initially demonstrated that associated bacteria confer a leaf beetle, Plagiodera versicolora, with the capability to resist the entomopathogenic fungus Aspergillus nomius infection, a capability sustained even under herbicide glyphosate stress. Further analysis of the associated microbiota revealed a significant alteration in abundance and composition due to glyphosate treatment. The dominant bacterium, post A. nomius infection or following a combination of glyphosate treatments, exhibited strong suppressive effects on fungal growth. Additionally, glyphosate markedly inhibited the pathogenic associated bacterium Pseudomonas though it inhibited P. versicolora’s immunity, ultimately enhancing the beetle's tolerance to A. nomius. In summary, our findings suggest that the leaf beetle's associated microbiota bestow an augmented resilience against the dual stressors of both the entomopathogen and glyphosate. These results provide insight into the effects of herbicide residues on interactions among insects, associated bacteria, and entomopathogenic fungi, holding significant implications for pest control and ecosystem assessment.
This study primarily showcases the protective role of associated bacteria in the leaf beetle Plagiodera versicolora against Aspergillus nomius infections. Further analysis of the associated microbiota revealed significant alteration in abundance and composition due to glyphosate treatment. The dominant bacterium, post A. nomius infection or following a combination of glyphosate treatment, exhibited strong suppressive effects on fungal growth. Additionally, glyphosate markedly inhibited the pathogenic associated bacterium Pseudomonas though it inhibited P. versicolora’s immunity, ultimately enhancing the beetle's tolerance to A. nomius. |
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This study primarily showcases the protective role of associated bacteria in the leaf beetle Plagiodera versicolora against Aspergillus nomius infections. Further analysis of the associated microbiota revealed significant alteration in abundance and composition due to glyphosate treatment. The dominant bacterium, post A. nomius infection or following a combination of glyphosate treatment, exhibited strong suppressive effects on fungal growth. Additionally, glyphosate markedly inhibited the pathogenic associated bacterium Pseudomonas though it inhibited P. versicolora’s immunity, ultimately enhancing the beetle's tolerance to A. nomius.</description><identifier>ISSN: 1749-4877</identifier><identifier>ISSN: 1749-4869</identifier><identifier>EISSN: 1749-4877</identifier><identifier>DOI: 10.1111/1749-4877.12812</identifier><identifier>PMID: 38379126</identifier><language>eng</language><publisher>Australia: Wiley Subscription Services, Inc</publisher><subject>Animals ; Aspergillus - drug effects ; associated microbiota ; Bacteria ; Bacteria - drug effects ; Chemical pest control ; Coleoptera - drug effects ; Coleoptera - microbiology ; Ecosystem assessment ; Entomopathogenic fungi ; Fungi ; Glycine - analogs & derivatives ; Glycine - pharmacology ; Glyphosate ; Herbicide residues ; Herbicides ; Herbicides - pharmacology ; Herbicides - toxicity ; Insects ; leaf beetle ; Leaves ; Microbial flora ; Microbiota ; Microbiota - drug effects ; Pathogens ; Pest control ; Pseudomonas - drug effects ; Stress, Physiological ; Virulence</subject><ispartof>Integrative zoology, 2024-11, Vol.19 (6), p.1092-1104</ispartof><rights>2024 International Society of Zoological Sciences, Institute of Zoology/Chinese Academy of Sciences and John Wiley & Sons Australia, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3722-632aa2982ad3bf12aae9d34210f40e4f0083628e5e05476bcf22cd8b7041ad753</citedby><cites>FETCH-LOGICAL-c3722-632aa2982ad3bf12aae9d34210f40e4f0083628e5e05476bcf22cd8b7041ad753</cites><orcidid>0000-0002-3270-0365</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2F1749-4877.12812$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2F1749-4877.12812$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1412,27905,27906,45555,45556</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38379126$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>ZHANG, Yuxin</creatorcontrib><creatorcontrib>XU, Handan</creatorcontrib><creatorcontrib>TU, Chengjie</creatorcontrib><creatorcontrib>HAN, Runhua</creatorcontrib><creatorcontrib>LUO, Jing</creatorcontrib><creatorcontrib>XU, Letian</creatorcontrib><title>Enhanced capacity of a leaf beetle to combat dual stress from entomopathogens and herbicides mediated by associated microbiota</title><title>Integrative zoology</title><addtitle>Integr Zool</addtitle><description>Herbicides have demonstrated their impact on insect fitness by affecting their associated microbiota or altering the virulence of entomopathogenic fungi toward insects. However, limited research has explored the implications of herbicide stress on the intricate tripartite interaction among insects, associated bacterial communities, and entomopathogens. In this study, we initially demonstrated that associated bacteria confer a leaf beetle, Plagiodera versicolora, with the capability to resist the entomopathogenic fungus Aspergillus nomius infection, a capability sustained even under herbicide glyphosate stress. Further analysis of the associated microbiota revealed a significant alteration in abundance and composition due to glyphosate treatment. The dominant bacterium, post A. nomius infection or following a combination of glyphosate treatments, exhibited strong suppressive effects on fungal growth. Additionally, glyphosate markedly inhibited the pathogenic associated bacterium Pseudomonas though it inhibited P. versicolora’s immunity, ultimately enhancing the beetle's tolerance to A. nomius. In summary, our findings suggest that the leaf beetle's associated microbiota bestow an augmented resilience against the dual stressors of both the entomopathogen and glyphosate. These results provide insight into the effects of herbicide residues on interactions among insects, associated bacteria, and entomopathogenic fungi, holding significant implications for pest control and ecosystem assessment.
This study primarily showcases the protective role of associated bacteria in the leaf beetle Plagiodera versicolora against Aspergillus nomius infections. Further analysis of the associated microbiota revealed significant alteration in abundance and composition due to glyphosate treatment. The dominant bacterium, post A. nomius infection or following a combination of glyphosate treatment, exhibited strong suppressive effects on fungal growth. Additionally, glyphosate markedly inhibited the pathogenic associated bacterium Pseudomonas though it inhibited P. versicolora’s immunity, ultimately enhancing the beetle's tolerance to A. nomius.</description><subject>Animals</subject><subject>Aspergillus - drug effects</subject><subject>associated microbiota</subject><subject>Bacteria</subject><subject>Bacteria - drug effects</subject><subject>Chemical pest control</subject><subject>Coleoptera - drug effects</subject><subject>Coleoptera - microbiology</subject><subject>Ecosystem assessment</subject><subject>Entomopathogenic fungi</subject><subject>Fungi</subject><subject>Glycine - analogs & derivatives</subject><subject>Glycine - pharmacology</subject><subject>Glyphosate</subject><subject>Herbicide residues</subject><subject>Herbicides</subject><subject>Herbicides - pharmacology</subject><subject>Herbicides - toxicity</subject><subject>Insects</subject><subject>leaf beetle</subject><subject>Leaves</subject><subject>Microbial flora</subject><subject>Microbiota</subject><subject>Microbiota - drug effects</subject><subject>Pathogens</subject><subject>Pest control</subject><subject>Pseudomonas - drug effects</subject><subject>Stress, Physiological</subject><subject>Virulence</subject><issn>1749-4877</issn><issn>1749-4869</issn><issn>1749-4877</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkb1vFDEQxS0EIiFQ0yFLNGku8ceud12iKCSRImhIk8Ya22Nuo931YXuFruFvx5cNEaLBjT2jn59m3iPkPWdnvJ5z3jV60_Rdd8ZFz8ULcvzcefnX-4i8yfmBMcVa1b4mR7KXneZCHZNfl_MWZoeeOtiBG8qexkCBjgiBWsQyIi2RujhZKNQvMNJcEuZMQ4oTxbnEKe6gbON3nDOF2dMtJju4wWOmE_oBShW3ewo5R7dW0-BStEMs8Ja8CjBmfPd0n5C7z5ffLq43t1-vbi4-3W6c7ITYKCkAhO4FeGkDrwVqLxvBWWgYNoGxXirRY4usbTplXRDC-d52rOHgu1aekNNVd5fijwVzMdOQHY4jzBiXbIQWupV9p3RFP_6DPsQlzXU6I7mQmmnFDtT5StVNck4YzC4NE6S94cwcojEH883BfPMYTf3x4Ul3sdWXZ_5PFhVQK_BzGHH_Pz1z8-VerMq_AVpCmUw</recordid><startdate>202411</startdate><enddate>202411</enddate><creator>ZHANG, Yuxin</creator><creator>XU, Handan</creator><creator>TU, Chengjie</creator><creator>HAN, Runhua</creator><creator>LUO, Jing</creator><creator>XU, Letian</creator><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SS</scope><scope>7TN</scope><scope>8FD</scope><scope>F1W</scope><scope>FR3</scope><scope>H95</scope><scope>H99</scope><scope>L.F</scope><scope>L.G</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-3270-0365</orcidid></search><sort><creationdate>202411</creationdate><title>Enhanced capacity of a leaf beetle to combat dual stress from entomopathogens and herbicides mediated by associated microbiota</title><author>ZHANG, Yuxin ; 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However, limited research has explored the implications of herbicide stress on the intricate tripartite interaction among insects, associated bacterial communities, and entomopathogens. In this study, we initially demonstrated that associated bacteria confer a leaf beetle, Plagiodera versicolora, with the capability to resist the entomopathogenic fungus Aspergillus nomius infection, a capability sustained even under herbicide glyphosate stress. Further analysis of the associated microbiota revealed a significant alteration in abundance and composition due to glyphosate treatment. The dominant bacterium, post A. nomius infection or following a combination of glyphosate treatments, exhibited strong suppressive effects on fungal growth. Additionally, glyphosate markedly inhibited the pathogenic associated bacterium Pseudomonas though it inhibited P. versicolora’s immunity, ultimately enhancing the beetle's tolerance to A. nomius. In summary, our findings suggest that the leaf beetle's associated microbiota bestow an augmented resilience against the dual stressors of both the entomopathogen and glyphosate. These results provide insight into the effects of herbicide residues on interactions among insects, associated bacteria, and entomopathogenic fungi, holding significant implications for pest control and ecosystem assessment.
This study primarily showcases the protective role of associated bacteria in the leaf beetle Plagiodera versicolora against Aspergillus nomius infections. Further analysis of the associated microbiota revealed significant alteration in abundance and composition due to glyphosate treatment. The dominant bacterium, post A. nomius infection or following a combination of glyphosate treatment, exhibited strong suppressive effects on fungal growth. Additionally, glyphosate markedly inhibited the pathogenic associated bacterium Pseudomonas though it inhibited P. versicolora’s immunity, ultimately enhancing the beetle's tolerance to A. nomius.</abstract><cop>Australia</cop><pub>Wiley Subscription Services, Inc</pub><pmid>38379126</pmid><doi>10.1111/1749-4877.12812</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0002-3270-0365</orcidid></addata></record> |
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subjects | Animals Aspergillus - drug effects associated microbiota Bacteria Bacteria - drug effects Chemical pest control Coleoptera - drug effects Coleoptera - microbiology Ecosystem assessment Entomopathogenic fungi Fungi Glycine - analogs & derivatives Glycine - pharmacology Glyphosate Herbicide residues Herbicides Herbicides - pharmacology Herbicides - toxicity Insects leaf beetle Leaves Microbial flora Microbiota Microbiota - drug effects Pathogens Pest control Pseudomonas - drug effects Stress, Physiological Virulence |
title | Enhanced capacity of a leaf beetle to combat dual stress from entomopathogens and herbicides mediated by associated microbiota |
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