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Different roles of host and habitat in determining the microbial communities of plant-feeding true bugs

BACKGROUND: The true bugs (Heteroptera) occupy nearly all of the known ecological niches of insects. Among them, as a group containing more than 30,000 species, the phytophagous true bugs are making increasing impacts on agricultural and forestry ecosystems. Previous studies proved that symbiotic ba...

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Autores principales: Yang, Zi-Wen, Luo, Jiu-Yang, Men, Yu, Liu, Zhi-Hui, Zheng, Zi-Kai, Wang, Yan-Hui, Xie, Qiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10629178/
https://www.ncbi.nlm.nih.gov/pubmed/37932839
http://dx.doi.org/10.1186/s40168-023-01702-y
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author Yang, Zi-Wen
Luo, Jiu-Yang
Men, Yu
Liu, Zhi-Hui
Zheng, Zi-Kai
Wang, Yan-Hui
Xie, Qiang
author_facet Yang, Zi-Wen
Luo, Jiu-Yang
Men, Yu
Liu, Zhi-Hui
Zheng, Zi-Kai
Wang, Yan-Hui
Xie, Qiang
author_sort Yang, Zi-Wen
collection PubMed
description BACKGROUND: The true bugs (Heteroptera) occupy nearly all of the known ecological niches of insects. Among them, as a group containing more than 30,000 species, the phytophagous true bugs are making increasing impacts on agricultural and forestry ecosystems. Previous studies proved that symbiotic bacteria play important roles in these insects in fitting various habitats. However, it is still obscure about the evolutionary and ecological patterns of the microorganisms of phytophagous true bugs as a whole with comprehensive taxon sampling. RESULTS: Here, in order to explore the symbiotic patterns between plant-feeding true bugs and their symbiotic microorganisms, 209 species belonging to 32 families of 9 superfamilies had been sampled, which covered all the major phytophagous families of true bugs. The symbiotic microbial communities were surveyed by full-length 16S rRNA gene and ITS amplicons respectively for bacteria and fungi using the PacBio platform. We revealed that hosts mainly affect the dominant bacteria of symbiotic microbial communities, while habitats generally influence the subordinate ones. Thereafter, we carried out the ancestral state reconstruction of the dominant bacteria and found that dramatic replacements of dominant bacteria occurred in the early Cretaceous and formed newly stable symbiotic relationships accompanying the radiation of insect families. In contrast, the symbiotic fungi were revealed to be horizontally transmitted, which makes fungal communities distinctive in different habitats but not significantly related to hosts. CONCLUSIONS: Host and habitat determine microbial communities of plant-feeding true bugs in different roles. The symbiotic bacterial communities are both shaped by host and habitat but in different ways. Nevertheless, the symbiotic fungal communities are mainly influenced by habitat but not host. These findings shed light on a general framework for future microbiome research of phytophagous insects. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-023-01702-y.
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spelling pubmed-106291782023-11-08 Different roles of host and habitat in determining the microbial communities of plant-feeding true bugs Yang, Zi-Wen Luo, Jiu-Yang Men, Yu Liu, Zhi-Hui Zheng, Zi-Kai Wang, Yan-Hui Xie, Qiang Microbiome Research BACKGROUND: The true bugs (Heteroptera) occupy nearly all of the known ecological niches of insects. Among them, as a group containing more than 30,000 species, the phytophagous true bugs are making increasing impacts on agricultural and forestry ecosystems. Previous studies proved that symbiotic bacteria play important roles in these insects in fitting various habitats. However, it is still obscure about the evolutionary and ecological patterns of the microorganisms of phytophagous true bugs as a whole with comprehensive taxon sampling. RESULTS: Here, in order to explore the symbiotic patterns between plant-feeding true bugs and their symbiotic microorganisms, 209 species belonging to 32 families of 9 superfamilies had been sampled, which covered all the major phytophagous families of true bugs. The symbiotic microbial communities were surveyed by full-length 16S rRNA gene and ITS amplicons respectively for bacteria and fungi using the PacBio platform. We revealed that hosts mainly affect the dominant bacteria of symbiotic microbial communities, while habitats generally influence the subordinate ones. Thereafter, we carried out the ancestral state reconstruction of the dominant bacteria and found that dramatic replacements of dominant bacteria occurred in the early Cretaceous and formed newly stable symbiotic relationships accompanying the radiation of insect families. In contrast, the symbiotic fungi were revealed to be horizontally transmitted, which makes fungal communities distinctive in different habitats but not significantly related to hosts. CONCLUSIONS: Host and habitat determine microbial communities of plant-feeding true bugs in different roles. The symbiotic bacterial communities are both shaped by host and habitat but in different ways. Nevertheless, the symbiotic fungal communities are mainly influenced by habitat but not host. These findings shed light on a general framework for future microbiome research of phytophagous insects. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-023-01702-y. BioMed Central 2023-11-07 /pmc/articles/PMC10629178/ /pubmed/37932839 http://dx.doi.org/10.1186/s40168-023-01702-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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
Yang, Zi-Wen
Luo, Jiu-Yang
Men, Yu
Liu, Zhi-Hui
Zheng, Zi-Kai
Wang, Yan-Hui
Xie, Qiang
Different roles of host and habitat in determining the microbial communities of plant-feeding true bugs
title Different roles of host and habitat in determining the microbial communities of plant-feeding true bugs
title_full Different roles of host and habitat in determining the microbial communities of plant-feeding true bugs
title_fullStr Different roles of host and habitat in determining the microbial communities of plant-feeding true bugs
title_full_unstemmed Different roles of host and habitat in determining the microbial communities of plant-feeding true bugs
title_short Different roles of host and habitat in determining the microbial communities of plant-feeding true bugs
title_sort different roles of host and habitat in determining the microbial communities of plant-feeding true bugs
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10629178/
https://www.ncbi.nlm.nih.gov/pubmed/37932839
http://dx.doi.org/10.1186/s40168-023-01702-y
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