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Geography, seasonality, and host‐associated population structure influence the fecal microbiome of a genetically depauparate Arctic mammal

The Canadian Arctic is an extreme environment with low floral and faunal diversity characterized by major seasonal shifts in temperature, moisture, and daylight. Muskoxen (Ovibos moschatus) are one of few large herbivores able to survive this harsh environment. Microbiome research of the gastrointes...

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Autores principales: Bird, Samantha, Prewer, Erin, Kutz, Susan, Leclerc, Lisa‐Marie, Vilaça, Sibelle T., Kyle, Christopher J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6912892/
https://www.ncbi.nlm.nih.gov/pubmed/31871639
http://dx.doi.org/10.1002/ece3.5768
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author Bird, Samantha
Prewer, Erin
Kutz, Susan
Leclerc, Lisa‐Marie
Vilaça, Sibelle T.
Kyle, Christopher J.
author_facet Bird, Samantha
Prewer, Erin
Kutz, Susan
Leclerc, Lisa‐Marie
Vilaça, Sibelle T.
Kyle, Christopher J.
author_sort Bird, Samantha
collection PubMed
description The Canadian Arctic is an extreme environment with low floral and faunal diversity characterized by major seasonal shifts in temperature, moisture, and daylight. Muskoxen (Ovibos moschatus) are one of few large herbivores able to survive this harsh environment. Microbiome research of the gastrointestinal tract may hold clues as to how muskoxen exist in the Arctic, but also how this species may respond to rapid environmental changes. In this study, we investigated the effects of season (spring/summer/winter), year (2007–2016), and host genetic structure on population‐level microbiome variation in muskoxen from the Canadian Arctic. We utilized 16S rRNA gene sequencing to characterize the fecal microbial communities of 78 male muskoxen encompassing two population genetic clusters. These clusters are defined by Arctic Mainland and Island populations, including the following: (a) two mainland sampling locations of the Northwest Territories and Nunavut and (b) four locations of Victoria Island. Between these geographic populations, we found that differences in the microbiome reflected host‐associated genetic cluster with evidence of migration. Within populations, seasonality influenced bacterial diversity with no significant differences between years of sampling. We found evidence of pathogenic bacteria, with significantly higher presence in mainland samples. Our findings demonstrate the effects of seasonality and the role of host population‐level structure in driving fecal microbiome differences in a large Arctic mammal.
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spelling pubmed-69128922019-12-23 Geography, seasonality, and host‐associated population structure influence the fecal microbiome of a genetically depauparate Arctic mammal Bird, Samantha Prewer, Erin Kutz, Susan Leclerc, Lisa‐Marie Vilaça, Sibelle T. Kyle, Christopher J. Ecol Evol Original Research The Canadian Arctic is an extreme environment with low floral and faunal diversity characterized by major seasonal shifts in temperature, moisture, and daylight. Muskoxen (Ovibos moschatus) are one of few large herbivores able to survive this harsh environment. Microbiome research of the gastrointestinal tract may hold clues as to how muskoxen exist in the Arctic, but also how this species may respond to rapid environmental changes. In this study, we investigated the effects of season (spring/summer/winter), year (2007–2016), and host genetic structure on population‐level microbiome variation in muskoxen from the Canadian Arctic. We utilized 16S rRNA gene sequencing to characterize the fecal microbial communities of 78 male muskoxen encompassing two population genetic clusters. These clusters are defined by Arctic Mainland and Island populations, including the following: (a) two mainland sampling locations of the Northwest Territories and Nunavut and (b) four locations of Victoria Island. Between these geographic populations, we found that differences in the microbiome reflected host‐associated genetic cluster with evidence of migration. Within populations, seasonality influenced bacterial diversity with no significant differences between years of sampling. We found evidence of pathogenic bacteria, with significantly higher presence in mainland samples. Our findings demonstrate the effects of seasonality and the role of host population‐level structure in driving fecal microbiome differences in a large Arctic mammal. John Wiley and Sons Inc. 2019-11-12 /pmc/articles/PMC6912892/ /pubmed/31871639 http://dx.doi.org/10.1002/ece3.5768 Text en © 2019 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Bird, Samantha
Prewer, Erin
Kutz, Susan
Leclerc, Lisa‐Marie
Vilaça, Sibelle T.
Kyle, Christopher J.
Geography, seasonality, and host‐associated population structure influence the fecal microbiome of a genetically depauparate Arctic mammal
title Geography, seasonality, and host‐associated population structure influence the fecal microbiome of a genetically depauparate Arctic mammal
title_full Geography, seasonality, and host‐associated population structure influence the fecal microbiome of a genetically depauparate Arctic mammal
title_fullStr Geography, seasonality, and host‐associated population structure influence the fecal microbiome of a genetically depauparate Arctic mammal
title_full_unstemmed Geography, seasonality, and host‐associated population structure influence the fecal microbiome of a genetically depauparate Arctic mammal
title_short Geography, seasonality, and host‐associated population structure influence the fecal microbiome of a genetically depauparate Arctic mammal
title_sort geography, seasonality, and host‐associated population structure influence the fecal microbiome of a genetically depauparate arctic mammal
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6912892/
https://www.ncbi.nlm.nih.gov/pubmed/31871639
http://dx.doi.org/10.1002/ece3.5768
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