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Soil-derived bacteria endow Camellia weevil with more ability to resist plant chemical defense
BACKGROUND: Herbivorous insects acquire their gut microbiota from diverse sources, and these microorganisms play significant roles in insect hosts’ tolerance to plant secondary defensive compounds. Camellia weevil (Curculio chinensis) (CW) is an obligate seed parasite of Camellia oleifera plants. Ou...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9233397/ https://www.ncbi.nlm.nih.gov/pubmed/35752840 http://dx.doi.org/10.1186/s40168-022-01290-3 |
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author | Zhang, Shouke Li, Zikun Shu, Jinping Xue, Huaijun Guo, Kai Zhou, Xudong |
author_facet | Zhang, Shouke Li, Zikun Shu, Jinping Xue, Huaijun Guo, Kai Zhou, Xudong |
author_sort | Zhang, Shouke |
collection | PubMed |
description | BACKGROUND: Herbivorous insects acquire their gut microbiota from diverse sources, and these microorganisms play significant roles in insect hosts’ tolerance to plant secondary defensive compounds. Camellia weevil (Curculio chinensis) (CW) is an obligate seed parasite of Camellia oleifera plants. Our previous study linked the CW’s gut microbiome to the tolerance of the tea saponin (TS) in C. oleifera seeds. However, the source of these gut microbiomes, the key bacteria involved in TS tolerance, and the degradation functions of these bacteria remain unresolved. RESULTS: Our study indicated that CW gut microbiome was more affected by the microbiome from soil than that from fruits. The soil-derived Acinetobacter served as the core bacterial genus, and Acinetobacter sp. was putatively regarded responsible for the saponin-degradation in CW guts. Subsequent experiments using fluorescently labeled cultures verified that the isolate Acinetobacter sp. AS23 can migrate into CW larval guts, and ultimately endow its host with the ability to degrade saponin, thereby allowing CW to subsist as a pest within plant fruits resisting to higher concentration of defensive chemical. CONCLUSIONS: The systematic studies of the sources of gut microorganisms, the screening of taxa involved in plant secondary metabolite degradation, and the investigation of bacteria responsible for CW toxicity mitigation provide clarified evidence that the intestinal microorganisms can mediate the tolerance of herbivorous insects against plant toxins. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-022-01290-3. |
format | Online Article Text |
id | pubmed-9233397 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-92333972022-06-26 Soil-derived bacteria endow Camellia weevil with more ability to resist plant chemical defense Zhang, Shouke Li, Zikun Shu, Jinping Xue, Huaijun Guo, Kai Zhou, Xudong Microbiome Research BACKGROUND: Herbivorous insects acquire their gut microbiota from diverse sources, and these microorganisms play significant roles in insect hosts’ tolerance to plant secondary defensive compounds. Camellia weevil (Curculio chinensis) (CW) is an obligate seed parasite of Camellia oleifera plants. Our previous study linked the CW’s gut microbiome to the tolerance of the tea saponin (TS) in C. oleifera seeds. However, the source of these gut microbiomes, the key bacteria involved in TS tolerance, and the degradation functions of these bacteria remain unresolved. RESULTS: Our study indicated that CW gut microbiome was more affected by the microbiome from soil than that from fruits. The soil-derived Acinetobacter served as the core bacterial genus, and Acinetobacter sp. was putatively regarded responsible for the saponin-degradation in CW guts. Subsequent experiments using fluorescently labeled cultures verified that the isolate Acinetobacter sp. AS23 can migrate into CW larval guts, and ultimately endow its host with the ability to degrade saponin, thereby allowing CW to subsist as a pest within plant fruits resisting to higher concentration of defensive chemical. CONCLUSIONS: The systematic studies of the sources of gut microorganisms, the screening of taxa involved in plant secondary metabolite degradation, and the investigation of bacteria responsible for CW toxicity mitigation provide clarified evidence that the intestinal microorganisms can mediate the tolerance of herbivorous insects against plant toxins. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-022-01290-3. BioMed Central 2022-06-25 /pmc/articles/PMC9233397/ /pubmed/35752840 http://dx.doi.org/10.1186/s40168-022-01290-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Zhang, Shouke Li, Zikun Shu, Jinping Xue, Huaijun Guo, Kai Zhou, Xudong Soil-derived bacteria endow Camellia weevil with more ability to resist plant chemical defense |
title | Soil-derived bacteria endow Camellia weevil with more ability to resist plant chemical defense |
title_full | Soil-derived bacteria endow Camellia weevil with more ability to resist plant chemical defense |
title_fullStr | Soil-derived bacteria endow Camellia weevil with more ability to resist plant chemical defense |
title_full_unstemmed | Soil-derived bacteria endow Camellia weevil with more ability to resist plant chemical defense |
title_short | Soil-derived bacteria endow Camellia weevil with more ability to resist plant chemical defense |
title_sort | soil-derived bacteria endow camellia weevil with more ability to resist plant chemical defense |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9233397/ https://www.ncbi.nlm.nih.gov/pubmed/35752840 http://dx.doi.org/10.1186/s40168-022-01290-3 |
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