Cargando…

Within‐community variation of interspecific divergence patterns in passerine gut microbiota

Gut microbiota (GM) often exhibit variation between different host species and co‐divergence with hosts' phylogeny. Identifying these patterns is a key for understanding the mechanisms that shaped symbiosis between GM and its hosts. Therefore, both GM‐host species specificity and GM‐host co‐div...

Descripción completa

Detalles Bibliográficos
Autores principales: Kubovčiak, Jan, Schmiedová, Lucie, Albrecht, Tomáš, Těšický, Martin, Tomášek, Oldřich, Kauzálová, Tereza, Kreisinger, Jakub
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9251858/
https://www.ncbi.nlm.nih.gov/pubmed/35813907
http://dx.doi.org/10.1002/ece3.9071
_version_ 1784740124504883200
author Kubovčiak, Jan
Schmiedová, Lucie
Albrecht, Tomáš
Těšický, Martin
Tomášek, Oldřich
Kauzálová, Tereza
Kreisinger, Jakub
author_facet Kubovčiak, Jan
Schmiedová, Lucie
Albrecht, Tomáš
Těšický, Martin
Tomášek, Oldřich
Kauzálová, Tereza
Kreisinger, Jakub
author_sort Kubovčiak, Jan
collection PubMed
description Gut microbiota (GM) often exhibit variation between different host species and co‐divergence with hosts' phylogeny. Identifying these patterns is a key for understanding the mechanisms that shaped symbiosis between GM and its hosts. Therefore, both GM‐host species specificity and GM‐host co‐divergence have been investigated by numerous studies. However, most of them neglected a possibility that different groups of bacteria within GM can vary in the tightness of their association with the host. Consequently, unlike most of these studies, we aimed to directly address how the strength of GM‐host species specificity and GM‐host co‐divergence vary across different GM clades. We decomposed GM communities of 52 passerine species (394 individuals), characterized by 16S rRNA amplicon sequence variant (ASV) profiles, into monophyletic Binned Taxonomic units (BTUs). Subsequently, we analyzed strength of host species specificity and correlation with host phylogeny separately for resulting BTUs. We found that most BTUs exhibited significant host‐species specificity in their composition. Notably, BTUs exhibiting high host‐species specificity comprised bacterial taxa known to impact host's physiology and immune system. However, BTUs rarely displayed significant co‐divergence with host phylogeny, suggesting that passerine GM evolution is not shaped primarily through a shared evolutionary history between the host and its gut microbes.
format Online
Article
Text
id pubmed-9251858
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-92518582022-07-08 Within‐community variation of interspecific divergence patterns in passerine gut microbiota Kubovčiak, Jan Schmiedová, Lucie Albrecht, Tomáš Těšický, Martin Tomášek, Oldřich Kauzálová, Tereza Kreisinger, Jakub Ecol Evol Research Articles Gut microbiota (GM) often exhibit variation between different host species and co‐divergence with hosts' phylogeny. Identifying these patterns is a key for understanding the mechanisms that shaped symbiosis between GM and its hosts. Therefore, both GM‐host species specificity and GM‐host co‐divergence have been investigated by numerous studies. However, most of them neglected a possibility that different groups of bacteria within GM can vary in the tightness of their association with the host. Consequently, unlike most of these studies, we aimed to directly address how the strength of GM‐host species specificity and GM‐host co‐divergence vary across different GM clades. We decomposed GM communities of 52 passerine species (394 individuals), characterized by 16S rRNA amplicon sequence variant (ASV) profiles, into monophyletic Binned Taxonomic units (BTUs). Subsequently, we analyzed strength of host species specificity and correlation with host phylogeny separately for resulting BTUs. We found that most BTUs exhibited significant host‐species specificity in their composition. Notably, BTUs exhibiting high host‐species specificity comprised bacterial taxa known to impact host's physiology and immune system. However, BTUs rarely displayed significant co‐divergence with host phylogeny, suggesting that passerine GM evolution is not shaped primarily through a shared evolutionary history between the host and its gut microbes. John Wiley and Sons Inc. 2022-07-04 /pmc/articles/PMC9251858/ /pubmed/35813907 http://dx.doi.org/10.1002/ece3.9071 Text en © 2022 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Kubovčiak, Jan
Schmiedová, Lucie
Albrecht, Tomáš
Těšický, Martin
Tomášek, Oldřich
Kauzálová, Tereza
Kreisinger, Jakub
Within‐community variation of interspecific divergence patterns in passerine gut microbiota
title Within‐community variation of interspecific divergence patterns in passerine gut microbiota
title_full Within‐community variation of interspecific divergence patterns in passerine gut microbiota
title_fullStr Within‐community variation of interspecific divergence patterns in passerine gut microbiota
title_full_unstemmed Within‐community variation of interspecific divergence patterns in passerine gut microbiota
title_short Within‐community variation of interspecific divergence patterns in passerine gut microbiota
title_sort within‐community variation of interspecific divergence patterns in passerine gut microbiota
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9251858/
https://www.ncbi.nlm.nih.gov/pubmed/35813907
http://dx.doi.org/10.1002/ece3.9071
work_keys_str_mv AT kubovciakjan withincommunityvariationofinterspecificdivergencepatternsinpasserinegutmicrobiota
AT schmiedovalucie withincommunityvariationofinterspecificdivergencepatternsinpasserinegutmicrobiota
AT albrechttomas withincommunityvariationofinterspecificdivergencepatternsinpasserinegutmicrobiota
AT tesickymartin withincommunityvariationofinterspecificdivergencepatternsinpasserinegutmicrobiota
AT tomasekoldrich withincommunityvariationofinterspecificdivergencepatternsinpasserinegutmicrobiota
AT kauzalovatereza withincommunityvariationofinterspecificdivergencepatternsinpasserinegutmicrobiota
AT kreisingerjakub withincommunityvariationofinterspecificdivergencepatternsinpasserinegutmicrobiota