The Gut Microbiota in Camellia Weevils Are Influenced by Plant Secondary Metabolites and Contribute to Saponin Degradation

ABSTRACT The camellia weevil (CW [Curculio chinensis]) is a notorious host-specific predator of the seeds of Camellia species in China, causing seed losses of up to 60%. The weevil is capable of overcoming host tree chemical defenses, while the mechanisms of how these beetles contend with the toxic...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Shouke Zhang, Jinping Shu, Huaijun Xue, Wei Zhang, Yabo Zhang, Yaning Liu, Linxin Fang, Yangdong Wang, Haojie Wang
Formato: article
Lenguaje:EN
Publicado: American Society for Microbiology 2020
Materias:
Acceso en línea:https://doaj.org/article/30b61ce98f2a4b7f85f9c2b99f0fd852
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:30b61ce98f2a4b7f85f9c2b99f0fd852
record_format dspace
spelling oai:doaj.org-article:30b61ce98f2a4b7f85f9c2b99f0fd8522021-12-02T18:15:46ZThe Gut Microbiota in Camellia Weevils Are Influenced by Plant Secondary Metabolites and Contribute to Saponin Degradation10.1128/mSystems.00692-192379-5077https://doaj.org/article/30b61ce98f2a4b7f85f9c2b99f0fd8522020-04-01T00:00:00Zhttps://journals.asm.org/doi/10.1128/mSystems.00692-19https://doaj.org/toc/2379-5077ABSTRACT The camellia weevil (CW [Curculio chinensis]) is a notorious host-specific predator of the seeds of Camellia species in China, causing seed losses of up to 60%. The weevil is capable of overcoming host tree chemical defenses, while the mechanisms of how these beetles contend with the toxic compounds are still unknown. Here, we examined the interaction between the gut microbes of CW and camellia seed chemistry and found that beetle-associated bacterial symbionts mediate tea saponin degradation. We demonstrate that the gut microbial community profile of CW was significantly plant associated, and the gut bacterial community associated with CW feeding on Camellia oleifera seeds is enriched with genes involved in tea saponin degradation compared with those feeding on Camellia sinensis and Camellia reticulata seeds. Twenty-seven bacteria from the genera Enterobacter, Serratia, Acinetobacter, and Micrococcus subsisted on tea saponin as a sole source of carbon and nitrogen, and Acinetobacter species are identified as being involved in the degradation of tea saponin. Our results provide the first metagenome of gut bacterial communities associated with a specialist insect pest of Camellia trees, and the results are consistent with a potential microbial contribution to the detoxification of tree-defensive chemicals. IMPORTANCE The gut microbiome may play an important role in insect-plant interactions mediated by plant secondary metabolites, but the microbial communities and functions of toxic plant feeders are still poorly characterized. In the present study, we provide the first metagenome of gut bacterial communities associated with a specialist weevil feeding on saponin-rich and saponin-low camellia seeds, and the results reveal the correlation between bacterial diversity and plant allelochemicals. We also used cultured microbes to establish their saponin-degradative capacity outside the insect. Our results provide new experimental context to better understand how gut microbial communities are influenced by plant secondary metabolites and how the resistance mechanisms involving microbes have evolved to deal with the chemical defenses of plants.Shouke ZhangJinping ShuHuaijun XueWei ZhangYabo ZhangYaning LiuLinxin FangYangdong WangHaojie WangAmerican Society for MicrobiologyarticleCamellia weevildegradationdiversitygut microbiomephytophagous insectplant secondary metabolitesMicrobiologyQR1-502ENmSystems, Vol 5, Iss 2 (2020)
institution DOAJ
collection DOAJ
language EN
topic Camellia weevil
degradation
diversity
gut microbiome
phytophagous insect
plant secondary metabolites
Microbiology
QR1-502
spellingShingle Camellia weevil
degradation
diversity
gut microbiome
phytophagous insect
plant secondary metabolites
Microbiology
QR1-502
Shouke Zhang
Jinping Shu
Huaijun Xue
Wei Zhang
Yabo Zhang
Yaning Liu
Linxin Fang
Yangdong Wang
Haojie Wang
The Gut Microbiota in Camellia Weevils Are Influenced by Plant Secondary Metabolites and Contribute to Saponin Degradation
description ABSTRACT The camellia weevil (CW [Curculio chinensis]) is a notorious host-specific predator of the seeds of Camellia species in China, causing seed losses of up to 60%. The weevil is capable of overcoming host tree chemical defenses, while the mechanisms of how these beetles contend with the toxic compounds are still unknown. Here, we examined the interaction between the gut microbes of CW and camellia seed chemistry and found that beetle-associated bacterial symbionts mediate tea saponin degradation. We demonstrate that the gut microbial community profile of CW was significantly plant associated, and the gut bacterial community associated with CW feeding on Camellia oleifera seeds is enriched with genes involved in tea saponin degradation compared with those feeding on Camellia sinensis and Camellia reticulata seeds. Twenty-seven bacteria from the genera Enterobacter, Serratia, Acinetobacter, and Micrococcus subsisted on tea saponin as a sole source of carbon and nitrogen, and Acinetobacter species are identified as being involved in the degradation of tea saponin. Our results provide the first metagenome of gut bacterial communities associated with a specialist insect pest of Camellia trees, and the results are consistent with a potential microbial contribution to the detoxification of tree-defensive chemicals. IMPORTANCE The gut microbiome may play an important role in insect-plant interactions mediated by plant secondary metabolites, but the microbial communities and functions of toxic plant feeders are still poorly characterized. In the present study, we provide the first metagenome of gut bacterial communities associated with a specialist weevil feeding on saponin-rich and saponin-low camellia seeds, and the results reveal the correlation between bacterial diversity and plant allelochemicals. We also used cultured microbes to establish their saponin-degradative capacity outside the insect. Our results provide new experimental context to better understand how gut microbial communities are influenced by plant secondary metabolites and how the resistance mechanisms involving microbes have evolved to deal with the chemical defenses of plants.
format article
author Shouke Zhang
Jinping Shu
Huaijun Xue
Wei Zhang
Yabo Zhang
Yaning Liu
Linxin Fang
Yangdong Wang
Haojie Wang
author_facet Shouke Zhang
Jinping Shu
Huaijun Xue
Wei Zhang
Yabo Zhang
Yaning Liu
Linxin Fang
Yangdong Wang
Haojie Wang
author_sort Shouke Zhang
title The Gut Microbiota in Camellia Weevils Are Influenced by Plant Secondary Metabolites and Contribute to Saponin Degradation
title_short The Gut Microbiota in Camellia Weevils Are Influenced by Plant Secondary Metabolites and Contribute to Saponin Degradation
title_full The Gut Microbiota in Camellia Weevils Are Influenced by Plant Secondary Metabolites and Contribute to Saponin Degradation
title_fullStr The Gut Microbiota in Camellia Weevils Are Influenced by Plant Secondary Metabolites and Contribute to Saponin Degradation
title_full_unstemmed The Gut Microbiota in Camellia Weevils Are Influenced by Plant Secondary Metabolites and Contribute to Saponin Degradation
title_sort gut microbiota in camellia weevils are influenced by plant secondary metabolites and contribute to saponin degradation
publisher American Society for Microbiology
publishDate 2020
url https://doaj.org/article/30b61ce98f2a4b7f85f9c2b99f0fd852
work_keys_str_mv AT shoukezhang thegutmicrobiotaincamelliaweevilsareinfluencedbyplantsecondarymetabolitesandcontributetosaponindegradation
AT jinpingshu thegutmicrobiotaincamelliaweevilsareinfluencedbyplantsecondarymetabolitesandcontributetosaponindegradation
AT huaijunxue thegutmicrobiotaincamelliaweevilsareinfluencedbyplantsecondarymetabolitesandcontributetosaponindegradation
AT weizhang thegutmicrobiotaincamelliaweevilsareinfluencedbyplantsecondarymetabolitesandcontributetosaponindegradation
AT yabozhang thegutmicrobiotaincamelliaweevilsareinfluencedbyplantsecondarymetabolitesandcontributetosaponindegradation
AT yaningliu thegutmicrobiotaincamelliaweevilsareinfluencedbyplantsecondarymetabolitesandcontributetosaponindegradation
AT linxinfang thegutmicrobiotaincamelliaweevilsareinfluencedbyplantsecondarymetabolitesandcontributetosaponindegradation
AT yangdongwang thegutmicrobiotaincamelliaweevilsareinfluencedbyplantsecondarymetabolitesandcontributetosaponindegradation
AT haojiewang thegutmicrobiotaincamelliaweevilsareinfluencedbyplantsecondarymetabolitesandcontributetosaponindegradation
AT shoukezhang gutmicrobiotaincamelliaweevilsareinfluencedbyplantsecondarymetabolitesandcontributetosaponindegradation
AT jinpingshu gutmicrobiotaincamelliaweevilsareinfluencedbyplantsecondarymetabolitesandcontributetosaponindegradation
AT huaijunxue gutmicrobiotaincamelliaweevilsareinfluencedbyplantsecondarymetabolitesandcontributetosaponindegradation
AT weizhang gutmicrobiotaincamelliaweevilsareinfluencedbyplantsecondarymetabolitesandcontributetosaponindegradation
AT yabozhang gutmicrobiotaincamelliaweevilsareinfluencedbyplantsecondarymetabolitesandcontributetosaponindegradation
AT yaningliu gutmicrobiotaincamelliaweevilsareinfluencedbyplantsecondarymetabolitesandcontributetosaponindegradation
AT linxinfang gutmicrobiotaincamelliaweevilsareinfluencedbyplantsecondarymetabolitesandcontributetosaponindegradation
AT yangdongwang gutmicrobiotaincamelliaweevilsareinfluencedbyplantsecondarymetabolitesandcontributetosaponindegradation
AT haojiewang gutmicrobiotaincamelliaweevilsareinfluencedbyplantsecondarymetabolitesandcontributetosaponindegradation
_version_ 1718378325314895872