Federico Musciotto, Begoña Dobon, Michael Greenacre, Alex Mira, Nikhil Chaudhary, Gul Deniz Salali, Pascale Gerbault, Rodolph Schlaepfer, Leonora H Astete, Marilyn Ngales, Jesus Gomez-Gardenes, Vito Latora, Federico Battiston, Jaume Bertranpetit, Lucio Vinicius, Andrea Bamberg Migliano
{"title":"Agta狩猎采集者的口腔微生物群是由接触网络结构形成的。","authors":"Federico Musciotto, Begoña Dobon, Michael Greenacre, Alex Mira, Nikhil Chaudhary, Gul Deniz Salali, Pascale Gerbault, Rodolph Schlaepfer, Leonora H Astete, Marilyn Ngales, Jesus Gomez-Gardenes, Vito Latora, Federico Battiston, Jaume Bertranpetit, Lucio Vinicius, Andrea Bamberg Migliano","doi":"10.1017/ehs.2023.4","DOIUrl":null,"url":null,"abstract":"<p><p>Here we investigate the effects of extensive sociality and mobility on the oral microbiome of 138 Agta hunter-gatherers from the Philippines. Our comparisons of microbiome composition showed that the Agta are more similar to Central African BaYaka hunter-gatherers than to neighbouring farmers. We also defined the Agta social microbiome as a set of 137 oral bacteria (only 7% of 1980 amplicon sequence variants) significantly influenced by social contact (quantified through wireless sensors of short-range interactions). We show that large interaction networks including strong links between close kin, spouses and even unrelated friends can significantly predict bacterial transmission networks across Agta camps. Finally, we show that more central individuals to social networks are also bacterial supersharers. We conclude that hunter-gatherer social microbiomes are predominantly pathogenic and were shaped by evolutionary tradeoffs between extensive sociality and disease spread.</p>","PeriodicalId":36414,"journal":{"name":"Evolutionary Human Sciences","volume":"5 ","pages":"e9"},"PeriodicalIF":2.2000,"publicationDate":"2023-02-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/3e/e0/S2513843X2300004Xa.PMC10426009.pdf","citationCount":"0","resultStr":"{\"title\":\"Agta hunter-gatherer oral microbiomes are shaped by contact network structure.\",\"authors\":\"Federico Musciotto, Begoña Dobon, Michael Greenacre, Alex Mira, Nikhil Chaudhary, Gul Deniz Salali, Pascale Gerbault, Rodolph Schlaepfer, Leonora H Astete, Marilyn Ngales, Jesus Gomez-Gardenes, Vito Latora, Federico Battiston, Jaume Bertranpetit, Lucio Vinicius, Andrea Bamberg Migliano\",\"doi\":\"10.1017/ehs.2023.4\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Here we investigate the effects of extensive sociality and mobility on the oral microbiome of 138 Agta hunter-gatherers from the Philippines. Our comparisons of microbiome composition showed that the Agta are more similar to Central African BaYaka hunter-gatherers than to neighbouring farmers. We also defined the Agta social microbiome as a set of 137 oral bacteria (only 7% of 1980 amplicon sequence variants) significantly influenced by social contact (quantified through wireless sensors of short-range interactions). We show that large interaction networks including strong links between close kin, spouses and even unrelated friends can significantly predict bacterial transmission networks across Agta camps. Finally, we show that more central individuals to social networks are also bacterial supersharers. We conclude that hunter-gatherer social microbiomes are predominantly pathogenic and were shaped by evolutionary tradeoffs between extensive sociality and disease spread.</p>\",\"PeriodicalId\":36414,\"journal\":{\"name\":\"Evolutionary Human Sciences\",\"volume\":\"5 \",\"pages\":\"e9\"},\"PeriodicalIF\":2.2000,\"publicationDate\":\"2023-02-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/3e/e0/S2513843X2300004Xa.PMC10426009.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Evolutionary Human Sciences\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1017/ehs.2023.4\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2023/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q1\",\"JCRName\":\"ANTHROPOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Evolutionary Human Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1017/ehs.2023.4","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/1/1 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"ANTHROPOLOGY","Score":null,"Total":0}
Agta hunter-gatherer oral microbiomes are shaped by contact network structure.
Here we investigate the effects of extensive sociality and mobility on the oral microbiome of 138 Agta hunter-gatherers from the Philippines. Our comparisons of microbiome composition showed that the Agta are more similar to Central African BaYaka hunter-gatherers than to neighbouring farmers. We also defined the Agta social microbiome as a set of 137 oral bacteria (only 7% of 1980 amplicon sequence variants) significantly influenced by social contact (quantified through wireless sensors of short-range interactions). We show that large interaction networks including strong links between close kin, spouses and even unrelated friends can significantly predict bacterial transmission networks across Agta camps. Finally, we show that more central individuals to social networks are also bacterial supersharers. We conclude that hunter-gatherer social microbiomes are predominantly pathogenic and were shaped by evolutionary tradeoffs between extensive sociality and disease spread.