Clifton D McKee, Alison J Peel, David T S Hayman, Richard Suu-Ire, Yaa Ntiamoa-Baidu, Andrew A Cunningham, James L N Wood, Colleen T Webb, Michael Y Kosoy
{"title":"外寄生虫和细菌的种群遗传学和群落结构显示了蝙蝠在岛链上的移动范围。","authors":"Clifton D McKee, Alison J Peel, David T S Hayman, Richard Suu-Ire, Yaa Ntiamoa-Baidu, Andrew A Cunningham, James L N Wood, Colleen T Webb, Michael Y Kosoy","doi":"10.1017/S0031182024000660","DOIUrl":null,"url":null,"abstract":"<p><p>Few studies have examined the genetic population structure of vector-borne microparasites in wildlife, making it unclear how much these systems can reveal about the movement of their associated hosts. This study examined the complex host–vector–microbe interactions in a system of bats, wingless ectoparasitic bat flies (Nycteribiidae), vector-borne microparasitic bacteria (<i>Bartonella</i>) and bacterial endosymbionts of flies (<i>Enterobacterales</i>) across an island chain in the Gulf of Guinea, West Africa. Limited population structure was found in bat flies and <i>Enterobacterales</i> symbionts compared to that of their hosts. Significant isolation by distance was observed in the dissimilarity of <i>Bartonella</i> communities detected in flies from sampled populations of <i>Eidolon helvum</i> bats. These patterns indicate that, while genetic dispersal of bats between islands is limited, some non-reproductive movements may lead to the dispersal of ectoparasites and associated microbes. This study deepens our knowledge of the phylogeography of African fruit bats, their ectoparasites and associated bacteria. The results presented could inform models of pathogen transmission in these bat populations and increase our theoretical understanding of community ecology in host–microbe systems.</p>","PeriodicalId":19967,"journal":{"name":"Parasitology","volume":" ","pages":"708-721"},"PeriodicalIF":2.1000,"publicationDate":"2024-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11474020/pdf/","citationCount":"0","resultStr":"{\"title\":\"Ectoparasite and bacterial population genetics and community structure indicate extent of bat movement across an island chain.\",\"authors\":\"Clifton D McKee, Alison J Peel, David T S Hayman, Richard Suu-Ire, Yaa Ntiamoa-Baidu, Andrew A Cunningham, James L N Wood, Colleen T Webb, Michael Y Kosoy\",\"doi\":\"10.1017/S0031182024000660\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Few studies have examined the genetic population structure of vector-borne microparasites in wildlife, making it unclear how much these systems can reveal about the movement of their associated hosts. This study examined the complex host–vector–microbe interactions in a system of bats, wingless ectoparasitic bat flies (Nycteribiidae), vector-borne microparasitic bacteria (<i>Bartonella</i>) and bacterial endosymbionts of flies (<i>Enterobacterales</i>) across an island chain in the Gulf of Guinea, West Africa. Limited population structure was found in bat flies and <i>Enterobacterales</i> symbionts compared to that of their hosts. Significant isolation by distance was observed in the dissimilarity of <i>Bartonella</i> communities detected in flies from sampled populations of <i>Eidolon helvum</i> bats. These patterns indicate that, while genetic dispersal of bats between islands is limited, some non-reproductive movements may lead to the dispersal of ectoparasites and associated microbes. This study deepens our knowledge of the phylogeography of African fruit bats, their ectoparasites and associated bacteria. The results presented could inform models of pathogen transmission in these bat populations and increase our theoretical understanding of community ecology in host–microbe systems.</p>\",\"PeriodicalId\":19967,\"journal\":{\"name\":\"Parasitology\",\"volume\":\" \",\"pages\":\"708-721\"},\"PeriodicalIF\":2.1000,\"publicationDate\":\"2024-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11474020/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Parasitology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1017/S0031182024000660\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/5/24 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"PARASITOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Parasitology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1017/S0031182024000660","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/5/24 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"PARASITOLOGY","Score":null,"Total":0}
Ectoparasite and bacterial population genetics and community structure indicate extent of bat movement across an island chain.
Few studies have examined the genetic population structure of vector-borne microparasites in wildlife, making it unclear how much these systems can reveal about the movement of their associated hosts. This study examined the complex host–vector–microbe interactions in a system of bats, wingless ectoparasitic bat flies (Nycteribiidae), vector-borne microparasitic bacteria (Bartonella) and bacterial endosymbionts of flies (Enterobacterales) across an island chain in the Gulf of Guinea, West Africa. Limited population structure was found in bat flies and Enterobacterales symbionts compared to that of their hosts. Significant isolation by distance was observed in the dissimilarity of Bartonella communities detected in flies from sampled populations of Eidolon helvum bats. These patterns indicate that, while genetic dispersal of bats between islands is limited, some non-reproductive movements may lead to the dispersal of ectoparasites and associated microbes. This study deepens our knowledge of the phylogeography of African fruit bats, their ectoparasites and associated bacteria. The results presented could inform models of pathogen transmission in these bat populations and increase our theoretical understanding of community ecology in host–microbe systems.
期刊介绍:
Parasitology is an important specialist journal covering the latest advances in the subject. It publishes original research and review papers on all aspects of parasitology and host-parasite relationships, including the latest discoveries in parasite biochemistry, molecular biology and genetics, ecology and epidemiology in the context of the biological, medical and veterinary sciences. Included in the subscription price are two special issues which contain reviews of current hot topics, one of which is the proceedings of the annual Symposia of the British Society for Parasitology, while the second, covering areas of significant topical interest, is commissioned by the editors and the editorial board.