How being synanthropic affects the gut bacteriome and mycobiome: comparison of two mouse species with contrasting ecologies

Abstract Background The vertebrate gastrointestinal tract is colonised by microbiota that have a major effect on the host’s health, physiology and phenotype. Once introduced into captivity, however, the gut microbial composition of free-living individuals can change dramatically. At present, little...

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Main Authors: Barbora Bendová, Jaroslav Piálek, Ľudovít Ďureje, Lucie Schmiedová, Dagmar Čížková, Jean-Francois Martin, Jakub Kreisinger
Format: Article
Language:English
Published: BMC 2020-07-01
Series:BMC Microbiology
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12866-020-01859-8
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spelling doaj-b3c32881683f4d40b194c1a5e7e409a62020-11-25T04:04:36ZengBMCBMC Microbiology1471-21802020-07-0120111310.1186/s12866-020-01859-8How being synanthropic affects the gut bacteriome and mycobiome: comparison of two mouse species with contrasting ecologiesBarbora Bendová0Jaroslav Piálek1Ľudovít Ďureje2Lucie Schmiedová3Dagmar Čížková4Jean-Francois Martin5Jakub Kreisinger6Department of Zoology, Faculty of Science, Charles UniversityStudenec Research Facility, Institute of Vertebrate Biology, Czech Academy of SciencesStudenec Research Facility, Institute of Vertebrate Biology, Czech Academy of SciencesDepartment of Zoology, Faculty of Science, Charles UniversityStudenec Research Facility, Institute of Vertebrate Biology, Czech Academy of SciencesCBGP, Montpellier SupAgro, INRA, CIRAD, IRD, Univ MontpellierDepartment of Zoology, Faculty of Science, Charles UniversityAbstract Background The vertebrate gastrointestinal tract is colonised by microbiota that have a major effect on the host’s health, physiology and phenotype. Once introduced into captivity, however, the gut microbial composition of free-living individuals can change dramatically. At present, little is known about gut microbial changes associated with adaptation to a synanthropic lifestyle in commensal species, compared with their non-commensal counterparts. Here, we compare the taxonomic composition and diversity of bacterial and fungal communities across three gut sections in synanthropic house mouse (Mus musculus) and a closely related non-synanthropic mound-building mouse (Mus spicilegus). Results Using Illumina sequencing of bacterial 16S rRNA amplicons, we found higher bacterial diversity in M. spicilegus and detected 11 bacterial operational taxonomic units with significantly different proportions. Notably, abundance of Oscillospira, which is typically higher in lean or outdoor pasturing animals, was more abundant in non-commensal M. spicilegus. ITS2-based barcoding revealed low diversity and high uniformity of gut fungi in both species, with the genus Kazachstania clearly dominant. Conclusions Though differences in gut bacteria observed in the two species can be associated with their close association with humans, changes due to a move from commensalism to captivity would appear to have caused larger shifts in microbiota.http://link.springer.com/article/10.1186/s12866-020-01859-8MicrobiomeMetabarcodingSteppe mouseMuridaeSymbiosisEvolution
collection DOAJ
language English
format Article
sources DOAJ
author Barbora Bendová
Jaroslav Piálek
Ľudovít Ďureje
Lucie Schmiedová
Dagmar Čížková
Jean-Francois Martin
Jakub Kreisinger
spellingShingle Barbora Bendová
Jaroslav Piálek
Ľudovít Ďureje
Lucie Schmiedová
Dagmar Čížková
Jean-Francois Martin
Jakub Kreisinger
How being synanthropic affects the gut bacteriome and mycobiome: comparison of two mouse species with contrasting ecologies
BMC Microbiology
Microbiome
Metabarcoding
Steppe mouse
Muridae
Symbiosis
Evolution
author_facet Barbora Bendová
Jaroslav Piálek
Ľudovít Ďureje
Lucie Schmiedová
Dagmar Čížková
Jean-Francois Martin
Jakub Kreisinger
author_sort Barbora Bendová
title How being synanthropic affects the gut bacteriome and mycobiome: comparison of two mouse species with contrasting ecologies
title_short How being synanthropic affects the gut bacteriome and mycobiome: comparison of two mouse species with contrasting ecologies
title_full How being synanthropic affects the gut bacteriome and mycobiome: comparison of two mouse species with contrasting ecologies
title_fullStr How being synanthropic affects the gut bacteriome and mycobiome: comparison of two mouse species with contrasting ecologies
title_full_unstemmed How being synanthropic affects the gut bacteriome and mycobiome: comparison of two mouse species with contrasting ecologies
title_sort how being synanthropic affects the gut bacteriome and mycobiome: comparison of two mouse species with contrasting ecologies
publisher BMC
series BMC Microbiology
issn 1471-2180
publishDate 2020-07-01
description Abstract Background The vertebrate gastrointestinal tract is colonised by microbiota that have a major effect on the host’s health, physiology and phenotype. Once introduced into captivity, however, the gut microbial composition of free-living individuals can change dramatically. At present, little is known about gut microbial changes associated with adaptation to a synanthropic lifestyle in commensal species, compared with their non-commensal counterparts. Here, we compare the taxonomic composition and diversity of bacterial and fungal communities across three gut sections in synanthropic house mouse (Mus musculus) and a closely related non-synanthropic mound-building mouse (Mus spicilegus). Results Using Illumina sequencing of bacterial 16S rRNA amplicons, we found higher bacterial diversity in M. spicilegus and detected 11 bacterial operational taxonomic units with significantly different proportions. Notably, abundance of Oscillospira, which is typically higher in lean or outdoor pasturing animals, was more abundant in non-commensal M. spicilegus. ITS2-based barcoding revealed low diversity and high uniformity of gut fungi in both species, with the genus Kazachstania clearly dominant. Conclusions Though differences in gut bacteria observed in the two species can be associated with their close association with humans, changes due to a move from commensalism to captivity would appear to have caused larger shifts in microbiota.
topic Microbiome
Metabarcoding
Steppe mouse
Muridae
Symbiosis
Evolution
url http://link.springer.com/article/10.1186/s12866-020-01859-8
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