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Unveiled feather microcosm: feather microbiota of passerine birds is closely associated with host species identity and bacteriocin-producing bacteria

The functional relevance of microbiota is a key aspect for understanding host–microbiota interactions. Mammalian skin harbours a complex consortium of beneficial microorganisms known to provide health and immune-boosting advantages. As yet, however, little is known about functional microbial communi...

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Autores principales: Javůrková, Veronika Gvoždíková, Kreisinger, Jakub, Procházka, Petr, Požgayová, Milica, Ševčíková, Kateřina, Brlík, Vojtěch, Adamík, Peter, Heneberg, Petr, Porkert, Jiří
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6775979/
https://www.ncbi.nlm.nih.gov/pubmed/31127178
http://dx.doi.org/10.1038/s41396-019-0438-4
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author Javůrková, Veronika Gvoždíková
Kreisinger, Jakub
Procházka, Petr
Požgayová, Milica
Ševčíková, Kateřina
Brlík, Vojtěch
Adamík, Peter
Heneberg, Petr
Porkert, Jiří
author_facet Javůrková, Veronika Gvoždíková
Kreisinger, Jakub
Procházka, Petr
Požgayová, Milica
Ševčíková, Kateřina
Brlík, Vojtěch
Adamík, Peter
Heneberg, Petr
Porkert, Jiří
author_sort Javůrková, Veronika Gvoždíková
collection PubMed
description The functional relevance of microbiota is a key aspect for understanding host–microbiota interactions. Mammalian skin harbours a complex consortium of beneficial microorganisms known to provide health and immune-boosting advantages. As yet, however, little is known about functional microbial communities on avian feathers, including their co-evolution with the host and factors determining feather microbiota (FM) diversity. Using 16S rRNA profiling, we investigated how host species identity, phylogeny and geographic origin determine FM in free-living passerine birds. Moreover, we estimated the relative abundance of bacteriocin-producing bacteria (BPB) and keratinolytic feather damaging bacteria (FDB) and evaluated the ability of BPB to affect FM diversity and relative abundance of FDB. Host species identity was associated with feather bacterial communities more strongly than host geographic origin. FM functional properties differed in terms of estimated BPB and FDB relative abundance, with both showing interspecific variation. FM diversity was negatively associated with BPB relative abundance across species, whereas BPB and FDB relative abundance was positively correlated. This study provides the first thorough evaluation of antimicrobial peptides-producing bacterial communities inhabiting the feather integument, including their likely potential to mediate niche-competition and to be associated with functional species-specific feather microbiota in avian hosts.
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spelling pubmed-67759792019-10-04 Unveiled feather microcosm: feather microbiota of passerine birds is closely associated with host species identity and bacteriocin-producing bacteria Javůrková, Veronika Gvoždíková Kreisinger, Jakub Procházka, Petr Požgayová, Milica Ševčíková, Kateřina Brlík, Vojtěch Adamík, Peter Heneberg, Petr Porkert, Jiří ISME J Article The functional relevance of microbiota is a key aspect for understanding host–microbiota interactions. Mammalian skin harbours a complex consortium of beneficial microorganisms known to provide health and immune-boosting advantages. As yet, however, little is known about functional microbial communities on avian feathers, including their co-evolution with the host and factors determining feather microbiota (FM) diversity. Using 16S rRNA profiling, we investigated how host species identity, phylogeny and geographic origin determine FM in free-living passerine birds. Moreover, we estimated the relative abundance of bacteriocin-producing bacteria (BPB) and keratinolytic feather damaging bacteria (FDB) and evaluated the ability of BPB to affect FM diversity and relative abundance of FDB. Host species identity was associated with feather bacterial communities more strongly than host geographic origin. FM functional properties differed in terms of estimated BPB and FDB relative abundance, with both showing interspecific variation. FM diversity was negatively associated with BPB relative abundance across species, whereas BPB and FDB relative abundance was positively correlated. This study provides the first thorough evaluation of antimicrobial peptides-producing bacterial communities inhabiting the feather integument, including their likely potential to mediate niche-competition and to be associated with functional species-specific feather microbiota in avian hosts. Nature Publishing Group UK 2019-05-24 2019-09 /pmc/articles/PMC6775979/ /pubmed/31127178 http://dx.doi.org/10.1038/s41396-019-0438-4 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Javůrková, Veronika Gvoždíková
Kreisinger, Jakub
Procházka, Petr
Požgayová, Milica
Ševčíková, Kateřina
Brlík, Vojtěch
Adamík, Peter
Heneberg, Petr
Porkert, Jiří
Unveiled feather microcosm: feather microbiota of passerine birds is closely associated with host species identity and bacteriocin-producing bacteria
title Unveiled feather microcosm: feather microbiota of passerine birds is closely associated with host species identity and bacteriocin-producing bacteria
title_full Unveiled feather microcosm: feather microbiota of passerine birds is closely associated with host species identity and bacteriocin-producing bacteria
title_fullStr Unveiled feather microcosm: feather microbiota of passerine birds is closely associated with host species identity and bacteriocin-producing bacteria
title_full_unstemmed Unveiled feather microcosm: feather microbiota of passerine birds is closely associated with host species identity and bacteriocin-producing bacteria
title_short Unveiled feather microcosm: feather microbiota of passerine birds is closely associated with host species identity and bacteriocin-producing bacteria
title_sort unveiled feather microcosm: feather microbiota of passerine birds is closely associated with host species identity and bacteriocin-producing bacteria
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6775979/
https://www.ncbi.nlm.nih.gov/pubmed/31127178
http://dx.doi.org/10.1038/s41396-019-0438-4
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