Cargando…

Cloacal Microbiome Structure in a Long-Distance Migratory Bird Assessed Using Deep 16sRNA Pyrosequencing

Effects of vertebrate-associated microbiota on physiology and health are of significant interest in current biological research. Most previous studies have focused on host-microbiota interactions in captive-bred mammalian models. These interactions and their outcomes are still relatively understudie...

Descripción completa

Detalles Bibliográficos
Autores principales: Kreisinger, Jakub, Čížková, Dagmar, Kropáčková, Lucie, Albrecht, Tomáš
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4567286/
https://www.ncbi.nlm.nih.gov/pubmed/26360776
http://dx.doi.org/10.1371/journal.pone.0137401
_version_ 1782389799713243136
author Kreisinger, Jakub
Čížková, Dagmar
Kropáčková, Lucie
Albrecht, Tomáš
author_facet Kreisinger, Jakub
Čížková, Dagmar
Kropáčková, Lucie
Albrecht, Tomáš
author_sort Kreisinger, Jakub
collection PubMed
description Effects of vertebrate-associated microbiota on physiology and health are of significant interest in current biological research. Most previous studies have focused on host-microbiota interactions in captive-bred mammalian models. These interactions and their outcomes are still relatively understudied, however, in wild populations and non-mammalian taxa. Using deep pyrosequencing, we described the cloacal microbiome (CM) composition in free living barn swallows Hirundo rustica, a long-distance migratory passerine bird. Barn swallow CM was dominated by bacteria of the Actinobacteria, Proteobacteria and Firmicutes phyla. Bacteroidetes, which represent an important proportion of the digestive tract microbiome in many vertebrate species, was relatively rare in barn swallow CM (< 5%). CM composition did not differ between males and females. A significant correlation of CM within breeding pair members is consistent with the hypothesis that cloacal contact during within-pair copulation may promote transfer of bacterial assemblages. This effect on CM composition had a relatively low effect size, however, possibly due to the species’ high level of sexual promiscuity.
format Online
Article
Text
id pubmed-4567286
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-45672862015-09-18 Cloacal Microbiome Structure in a Long-Distance Migratory Bird Assessed Using Deep 16sRNA Pyrosequencing Kreisinger, Jakub Čížková, Dagmar Kropáčková, Lucie Albrecht, Tomáš PLoS One Research Article Effects of vertebrate-associated microbiota on physiology and health are of significant interest in current biological research. Most previous studies have focused on host-microbiota interactions in captive-bred mammalian models. These interactions and their outcomes are still relatively understudied, however, in wild populations and non-mammalian taxa. Using deep pyrosequencing, we described the cloacal microbiome (CM) composition in free living barn swallows Hirundo rustica, a long-distance migratory passerine bird. Barn swallow CM was dominated by bacteria of the Actinobacteria, Proteobacteria and Firmicutes phyla. Bacteroidetes, which represent an important proportion of the digestive tract microbiome in many vertebrate species, was relatively rare in barn swallow CM (< 5%). CM composition did not differ between males and females. A significant correlation of CM within breeding pair members is consistent with the hypothesis that cloacal contact during within-pair copulation may promote transfer of bacterial assemblages. This effect on CM composition had a relatively low effect size, however, possibly due to the species’ high level of sexual promiscuity. Public Library of Science 2015-09-11 /pmc/articles/PMC4567286/ /pubmed/26360776 http://dx.doi.org/10.1371/journal.pone.0137401 Text en © 2015 Kreisinger et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Kreisinger, Jakub
Čížková, Dagmar
Kropáčková, Lucie
Albrecht, Tomáš
Cloacal Microbiome Structure in a Long-Distance Migratory Bird Assessed Using Deep 16sRNA Pyrosequencing
title Cloacal Microbiome Structure in a Long-Distance Migratory Bird Assessed Using Deep 16sRNA Pyrosequencing
title_full Cloacal Microbiome Structure in a Long-Distance Migratory Bird Assessed Using Deep 16sRNA Pyrosequencing
title_fullStr Cloacal Microbiome Structure in a Long-Distance Migratory Bird Assessed Using Deep 16sRNA Pyrosequencing
title_full_unstemmed Cloacal Microbiome Structure in a Long-Distance Migratory Bird Assessed Using Deep 16sRNA Pyrosequencing
title_short Cloacal Microbiome Structure in a Long-Distance Migratory Bird Assessed Using Deep 16sRNA Pyrosequencing
title_sort cloacal microbiome structure in a long-distance migratory bird assessed using deep 16srna pyrosequencing
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4567286/
https://www.ncbi.nlm.nih.gov/pubmed/26360776
http://dx.doi.org/10.1371/journal.pone.0137401
work_keys_str_mv AT kreisingerjakub cloacalmicrobiomestructureinalongdistancemigratorybirdassessedusingdeep16srnapyrosequencing
AT cizkovadagmar cloacalmicrobiomestructureinalongdistancemigratorybirdassessedusingdeep16srnapyrosequencing
AT kropackovalucie cloacalmicrobiomestructureinalongdistancemigratorybirdassessedusingdeep16srnapyrosequencing
AT albrechttomas cloacalmicrobiomestructureinalongdistancemigratorybirdassessedusingdeep16srnapyrosequencing