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Comparative Analyses of the Digestive Tract Microbiota of New Guinean Passerine Birds

The digestive tract microbiota (DTM) plays a plethora of functions that enable hosts to exploit novel niches. However, our understanding of the DTM of birds, particularly passerines, and the turnover of microbial communities along the digestive tract are limited. To better understand how passerine D...

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Autores principales: Bodawatta, Kasun H., Sam, Katerina, Jønsson, Knud A., Poulsen, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6097311/
https://www.ncbi.nlm.nih.gov/pubmed/30147680
http://dx.doi.org/10.3389/fmicb.2018.01830
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author Bodawatta, Kasun H.
Sam, Katerina
Jønsson, Knud A.
Poulsen, Michael
author_facet Bodawatta, Kasun H.
Sam, Katerina
Jønsson, Knud A.
Poulsen, Michael
author_sort Bodawatta, Kasun H.
collection PubMed
description The digestive tract microbiota (DTM) plays a plethora of functions that enable hosts to exploit novel niches. However, our understanding of the DTM of birds, particularly passerines, and the turnover of microbial communities along the digestive tract are limited. To better understand how passerine DTMs are assembled, and how the composition changes along the digestive tract, we investigated the DTM of seven different compartments along the digestive tract of nine New Guinean passerine bird species using Illumina MiSeq sequencing of the V4 region of the 16S rRNA. Overall, passerine DTMs were dominated by the phyla Firmicutes and Proteobacteria. We found bird species-specific DTM assemblages and the DTM of different compartments from the same species tended to cluster together. We also found a notable relationship between gut community similarity and feeding guilds (insectivores vs. omnivores). The dominant bacterial genera tended to differ between insectivores and omnivores, with insectivores mainly having lactic acid bacteria that may contribute to the breakdown of carbohydrates. Omnivorous DTMs were more diverse than insectivores and dominated by the bacterial phyla Proteobacteria and Tenericutes. These bacteria may contribute to nitrogen metabolism, and the diverse omnivorous DTMs may allow for more flexibility with varying food availability as these species have wider feeding niches. In well-sampled omnivorous species, the dominant bacterial genera changed along the digestive tracts, which was less prominent for insectivores. In conclusion, the DTMs of New Guinean passerines seem to be species specific and, at least in part, be shaped by bird diet. The sampling of DTM along the digestive tract improved capturing of a more complete set of members, with implications for our understanding of the interactions between symbiont and gut compartment functions.
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spelling pubmed-60973112018-08-24 Comparative Analyses of the Digestive Tract Microbiota of New Guinean Passerine Birds Bodawatta, Kasun H. Sam, Katerina Jønsson, Knud A. Poulsen, Michael Front Microbiol Microbiology The digestive tract microbiota (DTM) plays a plethora of functions that enable hosts to exploit novel niches. However, our understanding of the DTM of birds, particularly passerines, and the turnover of microbial communities along the digestive tract are limited. To better understand how passerine DTMs are assembled, and how the composition changes along the digestive tract, we investigated the DTM of seven different compartments along the digestive tract of nine New Guinean passerine bird species using Illumina MiSeq sequencing of the V4 region of the 16S rRNA. Overall, passerine DTMs were dominated by the phyla Firmicutes and Proteobacteria. We found bird species-specific DTM assemblages and the DTM of different compartments from the same species tended to cluster together. We also found a notable relationship between gut community similarity and feeding guilds (insectivores vs. omnivores). The dominant bacterial genera tended to differ between insectivores and omnivores, with insectivores mainly having lactic acid bacteria that may contribute to the breakdown of carbohydrates. Omnivorous DTMs were more diverse than insectivores and dominated by the bacterial phyla Proteobacteria and Tenericutes. These bacteria may contribute to nitrogen metabolism, and the diverse omnivorous DTMs may allow for more flexibility with varying food availability as these species have wider feeding niches. In well-sampled omnivorous species, the dominant bacterial genera changed along the digestive tracts, which was less prominent for insectivores. In conclusion, the DTMs of New Guinean passerines seem to be species specific and, at least in part, be shaped by bird diet. The sampling of DTM along the digestive tract improved capturing of a more complete set of members, with implications for our understanding of the interactions between symbiont and gut compartment functions. Frontiers Media S.A. 2018-08-10 /pmc/articles/PMC6097311/ /pubmed/30147680 http://dx.doi.org/10.3389/fmicb.2018.01830 Text en Copyright © 2018 Bodawatta, Sam, Jønsson and Poulsen. http://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
Bodawatta, Kasun H.
Sam, Katerina
Jønsson, Knud A.
Poulsen, Michael
Comparative Analyses of the Digestive Tract Microbiota of New Guinean Passerine Birds
title Comparative Analyses of the Digestive Tract Microbiota of New Guinean Passerine Birds
title_full Comparative Analyses of the Digestive Tract Microbiota of New Guinean Passerine Birds
title_fullStr Comparative Analyses of the Digestive Tract Microbiota of New Guinean Passerine Birds
title_full_unstemmed Comparative Analyses of the Digestive Tract Microbiota of New Guinean Passerine Birds
title_short Comparative Analyses of the Digestive Tract Microbiota of New Guinean Passerine Birds
title_sort comparative analyses of the digestive tract microbiota of new guinean passerine birds
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6097311/
https://www.ncbi.nlm.nih.gov/pubmed/30147680
http://dx.doi.org/10.3389/fmicb.2018.01830
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