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Family matters: skin microbiome reflects the social group and spatial proximity in wild zebra finches

BACKGROUND: So far, large numbers of studies investigating the microbiome have focused on gut microbiota and less have addressed the microbiome of the skin. Especially in avian taxa our understanding of the ecology and function of these bacteria remains incomplete. The involvement of skin bacteria i...

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Autores principales: Engel, Kathrin, Pankoke, Helga, Jünemann, Sebastian, Brandl, Hanja B., Sauer, Jan, Griffith, Simon C., Kalinowski, Jörn, Caspers, Barbara A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7664024/
https://www.ncbi.nlm.nih.gov/pubmed/33187490
http://dx.doi.org/10.1186/s12898-020-00326-2
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author Engel, Kathrin
Pankoke, Helga
Jünemann, Sebastian
Brandl, Hanja B.
Sauer, Jan
Griffith, Simon C.
Kalinowski, Jörn
Caspers, Barbara A.
author_facet Engel, Kathrin
Pankoke, Helga
Jünemann, Sebastian
Brandl, Hanja B.
Sauer, Jan
Griffith, Simon C.
Kalinowski, Jörn
Caspers, Barbara A.
author_sort Engel, Kathrin
collection PubMed
description BACKGROUND: So far, large numbers of studies investigating the microbiome have focused on gut microbiota and less have addressed the microbiome of the skin. Especially in avian taxa our understanding of the ecology and function of these bacteria remains incomplete. The involvement of skin bacteria in intra-specific communication has recently received attention, and has highlighted the need to understand what information is potentially being encoded in bacterial communities. Using next generation sequencing techniques, we characterised the skin microbiome of wild zebra finches, aiming to understand the impact of sex, age and group composition on skin bacteria communities. For this purpose, we sampled skin swabs from both sexes and two age classes (adults and nestlings) of 12 different zebra finch families and analysed the bacterial communities. RESULTS: Using 16S rRNA sequencing we found no effect of age, sex and family on bacterial diversity (alpha diversity). However, when comparing the composition (beta diversity), we found that animals of social groups (families) harbour highly similar bacterial communities on their skin with respect to community composition. Within families, closely related individuals shared significantly more bacterial taxa than non-related animals. In addition, we found that age (adults vs. nestlings) affected bacterial composition. Finally, we found that spatial proximity of nest sites, and therefore individuals, correlated with the skin microbiota similarity. CONCLUSIONS: Birds harbour very diverse and complex bacterial assemblages on their skin. These bacterial communities are distinguishable and characteristic for intraspecific social groups. Our findings are indicative for a family-specific skin microbiome in wild zebra finches. Genetics and the (social) environment seem to be the influential factors shaping the complex bacterial communities. Bacterial communities associated with the skin have a potential to emit volatiles and therefore these communities may play a role in intraspecific social communication, e.g. via signalling social group membership.
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spelling pubmed-76640242020-11-13 Family matters: skin microbiome reflects the social group and spatial proximity in wild zebra finches Engel, Kathrin Pankoke, Helga Jünemann, Sebastian Brandl, Hanja B. Sauer, Jan Griffith, Simon C. Kalinowski, Jörn Caspers, Barbara A. BMC Ecol Research Article BACKGROUND: So far, large numbers of studies investigating the microbiome have focused on gut microbiota and less have addressed the microbiome of the skin. Especially in avian taxa our understanding of the ecology and function of these bacteria remains incomplete. The involvement of skin bacteria in intra-specific communication has recently received attention, and has highlighted the need to understand what information is potentially being encoded in bacterial communities. Using next generation sequencing techniques, we characterised the skin microbiome of wild zebra finches, aiming to understand the impact of sex, age and group composition on skin bacteria communities. For this purpose, we sampled skin swabs from both sexes and two age classes (adults and nestlings) of 12 different zebra finch families and analysed the bacterial communities. RESULTS: Using 16S rRNA sequencing we found no effect of age, sex and family on bacterial diversity (alpha diversity). However, when comparing the composition (beta diversity), we found that animals of social groups (families) harbour highly similar bacterial communities on their skin with respect to community composition. Within families, closely related individuals shared significantly more bacterial taxa than non-related animals. In addition, we found that age (adults vs. nestlings) affected bacterial composition. Finally, we found that spatial proximity of nest sites, and therefore individuals, correlated with the skin microbiota similarity. CONCLUSIONS: Birds harbour very diverse and complex bacterial assemblages on their skin. These bacterial communities are distinguishable and characteristic for intraspecific social groups. Our findings are indicative for a family-specific skin microbiome in wild zebra finches. Genetics and the (social) environment seem to be the influential factors shaping the complex bacterial communities. Bacterial communities associated with the skin have a potential to emit volatiles and therefore these communities may play a role in intraspecific social communication, e.g. via signalling social group membership. BioMed Central 2020-11-13 /pmc/articles/PMC7664024/ /pubmed/33187490 http://dx.doi.org/10.1186/s12898-020-00326-2 Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Engel, Kathrin
Pankoke, Helga
Jünemann, Sebastian
Brandl, Hanja B.
Sauer, Jan
Griffith, Simon C.
Kalinowski, Jörn
Caspers, Barbara A.
Family matters: skin microbiome reflects the social group and spatial proximity in wild zebra finches
title Family matters: skin microbiome reflects the social group and spatial proximity in wild zebra finches
title_full Family matters: skin microbiome reflects the social group and spatial proximity in wild zebra finches
title_fullStr Family matters: skin microbiome reflects the social group and spatial proximity in wild zebra finches
title_full_unstemmed Family matters: skin microbiome reflects the social group and spatial proximity in wild zebra finches
title_short Family matters: skin microbiome reflects the social group and spatial proximity in wild zebra finches
title_sort family matters: skin microbiome reflects the social group and spatial proximity in wild zebra finches
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7664024/
https://www.ncbi.nlm.nih.gov/pubmed/33187490
http://dx.doi.org/10.1186/s12898-020-00326-2
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