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Social networks strongly predict the gut microbiota of wild mice
The mammalian gut teems with microbes, yet how hosts acquire these symbionts remains poorly understood. Research in primates suggests that microbes can be picked up via social contact, but the role of social interactions in non-group-living species remains underexplored. Here, we use a passive track...
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Published in: | The ISME Journal 2021-09, Vol.15 (9), p.2601-2613 |
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description | The mammalian gut teems with microbes, yet how hosts acquire these symbionts remains poorly understood. Research in primates suggests that microbes can be picked up via social contact, but the role of social interactions in non-group-living species remains underexplored. Here, we use a passive tracking system to collect high resolution spatiotemporal activity data from wild mice (
Apodemus sylvaticus
). Social network analysis revealed social association strength to be the strongest predictor of microbiota similarity among individuals, controlling for factors including spatial proximity and kinship, which had far smaller or nonsignificant effects. This social effect was limited to interactions involving males (male-male and male-female), implicating sex-dependent behaviours as driving processes. Social network position also predicted microbiota richness, with well-connected individuals having the most diverse microbiotas. Overall, these findings suggest social contact provides a key transmission pathway for gut symbionts even in relatively asocial mammals, that strongly shapes the adult gut microbiota. This work underlines the potential for individuals to pick up beneficial symbionts as well as pathogens from social interactions. |
doi_str_mv | 10.1038/s41396-021-00949-3 |
format | article |
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Apodemus sylvaticus
). Social network analysis revealed social association strength to be the strongest predictor of microbiota similarity among individuals, controlling for factors including spatial proximity and kinship, which had far smaller or nonsignificant effects. This social effect was limited to interactions involving males (male-male and male-female), implicating sex-dependent behaviours as driving processes. Social network position also predicted microbiota richness, with well-connected individuals having the most diverse microbiotas. Overall, these findings suggest social contact provides a key transmission pathway for gut symbionts even in relatively asocial mammals, that strongly shapes the adult gut microbiota. This work underlines the potential for individuals to pick up beneficial symbionts as well as pathogens from social interactions.</description><identifier>ISSN: 1751-7362</identifier><identifier>ISSN: 1751-7370</identifier><identifier>EISSN: 1751-7370</identifier><identifier>DOI: 10.1038/s41396-021-00949-3</identifier><identifier>PMID: 33731838</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>45 ; 45/22 ; 45/23 ; 45/77 ; 45/91 ; 631/158/853 ; 631/158/855 ; 631/601 ; Biomedical and Life Sciences ; Ecology ; Evolutionary Biology ; Intestinal microflora ; Life Sciences ; Males ; Mammals ; Microbial Ecology ; Microbial Genetics and Genomics ; Microbiology ; Microbiota ; Microorganisms ; Network analysis ; Sexual behavior ; Social behavior ; Social factors ; Social interactions ; Social networks ; Social organization ; Symbionts ; Tracking systems</subject><ispartof>The ISME Journal, 2021-09, Vol.15 (9), p.2601-2613</ispartof><rights>The Author(s) 2021</rights><rights>The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c577t-c056f8a26cb61a21dc1f0bdf35d2d4b2735c501c2831e19bff0326467f35ca2a3</citedby><cites>FETCH-LOGICAL-c577t-c056f8a26cb61a21dc1f0bdf35d2d4b2735c501c2831e19bff0326467f35ca2a3</cites><orcidid>0000-0001-8394-6229 ; 0000-0003-4860-7840 ; 0000-0002-2368-4623</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8397773/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8397773/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33731838$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-469034$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Raulo, Aura</creatorcontrib><creatorcontrib>Allen, Bryony E.</creatorcontrib><creatorcontrib>Troitsky, Tanya</creatorcontrib><creatorcontrib>Husby, Arild</creatorcontrib><creatorcontrib>Firth, Josh A.</creatorcontrib><creatorcontrib>Coulson, Tim</creatorcontrib><creatorcontrib>Knowles, Sarah C. L.</creatorcontrib><title>Social networks strongly predict the gut microbiota of wild mice</title><title>The ISME Journal</title><addtitle>ISME J</addtitle><addtitle>ISME J</addtitle><description>The mammalian gut teems with microbes, yet how hosts acquire these symbionts remains poorly understood. Research in primates suggests that microbes can be picked up via social contact, but the role of social interactions in non-group-living species remains underexplored. Here, we use a passive tracking system to collect high resolution spatiotemporal activity data from wild mice (
Apodemus sylvaticus
). Social network analysis revealed social association strength to be the strongest predictor of microbiota similarity among individuals, controlling for factors including spatial proximity and kinship, which had far smaller or nonsignificant effects. This social effect was limited to interactions involving males (male-male and male-female), implicating sex-dependent behaviours as driving processes. Social network position also predicted microbiota richness, with well-connected individuals having the most diverse microbiotas. Overall, these findings suggest social contact provides a key transmission pathway for gut symbionts even in relatively asocial mammals, that strongly shapes the adult gut microbiota. 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L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Social networks strongly predict the gut microbiota of wild mice</atitle><jtitle>The ISME Journal</jtitle><stitle>ISME J</stitle><addtitle>ISME J</addtitle><date>2021-09-01</date><risdate>2021</risdate><volume>15</volume><issue>9</issue><spage>2601</spage><epage>2613</epage><pages>2601-2613</pages><issn>1751-7362</issn><issn>1751-7370</issn><eissn>1751-7370</eissn><abstract>The mammalian gut teems with microbes, yet how hosts acquire these symbionts remains poorly understood. Research in primates suggests that microbes can be picked up via social contact, but the role of social interactions in non-group-living species remains underexplored. Here, we use a passive tracking system to collect high resolution spatiotemporal activity data from wild mice (
Apodemus sylvaticus
). Social network analysis revealed social association strength to be the strongest predictor of microbiota similarity among individuals, controlling for factors including spatial proximity and kinship, which had far smaller or nonsignificant effects. This social effect was limited to interactions involving males (male-male and male-female), implicating sex-dependent behaviours as driving processes. Social network position also predicted microbiota richness, with well-connected individuals having the most diverse microbiotas. Overall, these findings suggest social contact provides a key transmission pathway for gut symbionts even in relatively asocial mammals, that strongly shapes the adult gut microbiota. This work underlines the potential for individuals to pick up beneficial symbionts as well as pathogens from social interactions.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>33731838</pmid><doi>10.1038/s41396-021-00949-3</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0001-8394-6229</orcidid><orcidid>https://orcid.org/0000-0003-4860-7840</orcidid><orcidid>https://orcid.org/0000-0002-2368-4623</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 45 45/22 45/23 45/77 45/91 631/158/853 631/158/855 631/601 Biomedical and Life Sciences Ecology Evolutionary Biology Intestinal microflora Life Sciences Males Mammals Microbial Ecology Microbial Genetics and Genomics Microbiology Microbiota Microorganisms Network analysis Sexual behavior Social behavior Social factors Social interactions Social networks Social organization Symbionts Tracking systems |
title | Social networks strongly predict the gut microbiota of wild mice |
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