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Diversity and Function of Wolf Spider Gut Microbiota Revealed by Shotgun Metagenomics

Wolf spiders (Lycosidae) are crucial component of integrated pest management programs and the characteristics of their gut microbiota are known to play important roles in improving fitness and survival of the host. However, there are only few studies of the gut microbiota among closely related speci...

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Autores principales: Wu, Runbiao, Wang, Luyu, Xie, Jianping, Zhang, Zhisheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8718803/
https://www.ncbi.nlm.nih.gov/pubmed/34975785
http://dx.doi.org/10.3389/fmicb.2021.758794
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author Wu, Runbiao
Wang, Luyu
Xie, Jianping
Zhang, Zhisheng
author_facet Wu, Runbiao
Wang, Luyu
Xie, Jianping
Zhang, Zhisheng
author_sort Wu, Runbiao
collection PubMed
description Wolf spiders (Lycosidae) are crucial component of integrated pest management programs and the characteristics of their gut microbiota are known to play important roles in improving fitness and survival of the host. However, there are only few studies of the gut microbiota among closely related species of wolf spider. Whether wolf spiders gut microbiota vary with habitats remains unknown. Here, we used shotgun metagenomic sequencing to compare the gut microbiota of two wolf spider species, Pardosa agraria and P. laura from farmland and woodland ecosystems, respectively. The results show that the gut microbiota of Pardosa spiders is similar in richness and abundance. Approximately 27.3% of the gut microbiota of P. agraria comprises Proteobacteria, and approximately 34.4% of the gut microbiota of P. laura comprises Firmicutes. We assembled microbial genomes and found that the gut microbiota of P. laura are enriched in genes for carbohydrate metabolism. In contrast, those of P. agraria showed a higher proportion of genes encoding acetyltransferase, an enzyme involved in resistance to antibiotics. We reconstructed three high-quality and species-level microbial genomes: Vulcaniibacterium thermophilum, Anoxybacillus flavithermus and an unknown bacterium belonging to the family Simkaniaceae. Our results contribute to an understanding of the diversity and function of gut microbiota in closely related spiders.
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spelling pubmed-87188032022-01-01 Diversity and Function of Wolf Spider Gut Microbiota Revealed by Shotgun Metagenomics Wu, Runbiao Wang, Luyu Xie, Jianping Zhang, Zhisheng Front Microbiol Microbiology Wolf spiders (Lycosidae) are crucial component of integrated pest management programs and the characteristics of their gut microbiota are known to play important roles in improving fitness and survival of the host. However, there are only few studies of the gut microbiota among closely related species of wolf spider. Whether wolf spiders gut microbiota vary with habitats remains unknown. Here, we used shotgun metagenomic sequencing to compare the gut microbiota of two wolf spider species, Pardosa agraria and P. laura from farmland and woodland ecosystems, respectively. The results show that the gut microbiota of Pardosa spiders is similar in richness and abundance. Approximately 27.3% of the gut microbiota of P. agraria comprises Proteobacteria, and approximately 34.4% of the gut microbiota of P. laura comprises Firmicutes. We assembled microbial genomes and found that the gut microbiota of P. laura are enriched in genes for carbohydrate metabolism. In contrast, those of P. agraria showed a higher proportion of genes encoding acetyltransferase, an enzyme involved in resistance to antibiotics. We reconstructed three high-quality and species-level microbial genomes: Vulcaniibacterium thermophilum, Anoxybacillus flavithermus and an unknown bacterium belonging to the family Simkaniaceae. Our results contribute to an understanding of the diversity and function of gut microbiota in closely related spiders. Frontiers Media S.A. 2021-12-17 /pmc/articles/PMC8718803/ /pubmed/34975785 http://dx.doi.org/10.3389/fmicb.2021.758794 Text en Copyright © 2021 Wu, Wang, Xie and Zhang. https://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) and the copyright owner(s) 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
Wu, Runbiao
Wang, Luyu
Xie, Jianping
Zhang, Zhisheng
Diversity and Function of Wolf Spider Gut Microbiota Revealed by Shotgun Metagenomics
title Diversity and Function of Wolf Spider Gut Microbiota Revealed by Shotgun Metagenomics
title_full Diversity and Function of Wolf Spider Gut Microbiota Revealed by Shotgun Metagenomics
title_fullStr Diversity and Function of Wolf Spider Gut Microbiota Revealed by Shotgun Metagenomics
title_full_unstemmed Diversity and Function of Wolf Spider Gut Microbiota Revealed by Shotgun Metagenomics
title_short Diversity and Function of Wolf Spider Gut Microbiota Revealed by Shotgun Metagenomics
title_sort diversity and function of wolf spider gut microbiota revealed by shotgun metagenomics
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8718803/
https://www.ncbi.nlm.nih.gov/pubmed/34975785
http://dx.doi.org/10.3389/fmicb.2021.758794
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