Cargando…
Phylogenomic analysis of 589 metagenome-assembled genomes encompassing all major prokaryotic lineages from the gut of higher termites
“Higher” termites have been able to colonize all tropical and subtropical regions because of their ability to digest lignocellulose with the aid of their prokaryotic gut microbiota. Over the last decade, numerous studies based on 16S rRNA gene amplicon libraries have largely described both the taxon...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PeerJ Inc.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7024585/ https://www.ncbi.nlm.nih.gov/pubmed/32095380 http://dx.doi.org/10.7717/peerj.8614 |
_version_ | 1783498432593264640 |
---|---|
author | Hervé, Vincent Liu, Pengfei Dietrich, Carsten Sillam-Dussès, David Stiblik, Petr Šobotník, Jan Brune, Andreas |
author_facet | Hervé, Vincent Liu, Pengfei Dietrich, Carsten Sillam-Dussès, David Stiblik, Petr Šobotník, Jan Brune, Andreas |
author_sort | Hervé, Vincent |
collection | PubMed |
description | “Higher” termites have been able to colonize all tropical and subtropical regions because of their ability to digest lignocellulose with the aid of their prokaryotic gut microbiota. Over the last decade, numerous studies based on 16S rRNA gene amplicon libraries have largely described both the taxonomy and structure of the prokaryotic communities associated with termite guts. Host diet and microenvironmental conditions have emerged as the main factors structuring the microbial assemblages in the different gut compartments. Additionally, these molecular inventories have revealed the existence of termite-specific clusters that indicate coevolutionary processes in numerous prokaryotic lineages. However, for lack of representative isolates, the functional role of most lineages remains unclear. We reconstructed 589 metagenome-assembled genomes (MAGs) from the different gut compartments of eight higher termite species that encompass 17 prokaryotic phyla. By iteratively building genome trees for each clade, we significantly improved the initial automated assignment, frequently up to the genus level. We recovered MAGs from most of the termite-specific clusters in the radiation of, for example, Planctomycetes, Fibrobacteres, Bacteroidetes, Euryarchaeota, Bathyarchaeota, Spirochaetes, Saccharibacteria, and Firmicutes, which to date contained only few or no representative genomes. Moreover, the MAGs included abundant members of the termite gut microbiota. This dataset represents the largest genomic resource for arthropod-associated microorganisms available to date and contributes substantially to populating the tree of life. More importantly, it provides a backbone for studying the metabolic potential of the termite gut microbiota, including the key members involved in carbon and nitrogen biogeochemical cycles, and important clues that may help cultivating representatives of these understudied clades. |
format | Online Article Text |
id | pubmed-7024585 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | PeerJ Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-70245852020-02-24 Phylogenomic analysis of 589 metagenome-assembled genomes encompassing all major prokaryotic lineages from the gut of higher termites Hervé, Vincent Liu, Pengfei Dietrich, Carsten Sillam-Dussès, David Stiblik, Petr Šobotník, Jan Brune, Andreas PeerJ Bioinformatics “Higher” termites have been able to colonize all tropical and subtropical regions because of their ability to digest lignocellulose with the aid of their prokaryotic gut microbiota. Over the last decade, numerous studies based on 16S rRNA gene amplicon libraries have largely described both the taxonomy and structure of the prokaryotic communities associated with termite guts. Host diet and microenvironmental conditions have emerged as the main factors structuring the microbial assemblages in the different gut compartments. Additionally, these molecular inventories have revealed the existence of termite-specific clusters that indicate coevolutionary processes in numerous prokaryotic lineages. However, for lack of representative isolates, the functional role of most lineages remains unclear. We reconstructed 589 metagenome-assembled genomes (MAGs) from the different gut compartments of eight higher termite species that encompass 17 prokaryotic phyla. By iteratively building genome trees for each clade, we significantly improved the initial automated assignment, frequently up to the genus level. We recovered MAGs from most of the termite-specific clusters in the radiation of, for example, Planctomycetes, Fibrobacteres, Bacteroidetes, Euryarchaeota, Bathyarchaeota, Spirochaetes, Saccharibacteria, and Firmicutes, which to date contained only few or no representative genomes. Moreover, the MAGs included abundant members of the termite gut microbiota. This dataset represents the largest genomic resource for arthropod-associated microorganisms available to date and contributes substantially to populating the tree of life. More importantly, it provides a backbone for studying the metabolic potential of the termite gut microbiota, including the key members involved in carbon and nitrogen biogeochemical cycles, and important clues that may help cultivating representatives of these understudied clades. PeerJ Inc. 2020-02-13 /pmc/articles/PMC7024585/ /pubmed/32095380 http://dx.doi.org/10.7717/peerj.8614 Text en © 2020 Hervé et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited. |
spellingShingle | Bioinformatics Hervé, Vincent Liu, Pengfei Dietrich, Carsten Sillam-Dussès, David Stiblik, Petr Šobotník, Jan Brune, Andreas Phylogenomic analysis of 589 metagenome-assembled genomes encompassing all major prokaryotic lineages from the gut of higher termites |
title | Phylogenomic analysis of 589 metagenome-assembled genomes encompassing all major prokaryotic lineages from the gut of higher termites |
title_full | Phylogenomic analysis of 589 metagenome-assembled genomes encompassing all major prokaryotic lineages from the gut of higher termites |
title_fullStr | Phylogenomic analysis of 589 metagenome-assembled genomes encompassing all major prokaryotic lineages from the gut of higher termites |
title_full_unstemmed | Phylogenomic analysis of 589 metagenome-assembled genomes encompassing all major prokaryotic lineages from the gut of higher termites |
title_short | Phylogenomic analysis of 589 metagenome-assembled genomes encompassing all major prokaryotic lineages from the gut of higher termites |
title_sort | phylogenomic analysis of 589 metagenome-assembled genomes encompassing all major prokaryotic lineages from the gut of higher termites |
topic | Bioinformatics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7024585/ https://www.ncbi.nlm.nih.gov/pubmed/32095380 http://dx.doi.org/10.7717/peerj.8614 |
work_keys_str_mv | AT hervevincent phylogenomicanalysisof589metagenomeassembledgenomesencompassingallmajorprokaryoticlineagesfromthegutofhighertermites AT liupengfei phylogenomicanalysisof589metagenomeassembledgenomesencompassingallmajorprokaryoticlineagesfromthegutofhighertermites AT dietrichcarsten phylogenomicanalysisof589metagenomeassembledgenomesencompassingallmajorprokaryoticlineagesfromthegutofhighertermites AT sillamdussesdavid phylogenomicanalysisof589metagenomeassembledgenomesencompassingallmajorprokaryoticlineagesfromthegutofhighertermites AT stiblikpetr phylogenomicanalysisof589metagenomeassembledgenomesencompassingallmajorprokaryoticlineagesfromthegutofhighertermites AT sobotnikjan phylogenomicanalysisof589metagenomeassembledgenomesencompassingallmajorprokaryoticlineagesfromthegutofhighertermites AT bruneandreas phylogenomicanalysisof589metagenomeassembledgenomesencompassingallmajorprokaryoticlineagesfromthegutofhighertermites |