{"title":"宿主-寄生虫关联动态影响小褐肌虫(Myotis lucifugus, Le Conte 1831)外寄生虫的传播和群体遗传","authors":"Alexandra H. Sauk, Hugh G. Broders","doi":"10.1002/ece3.71233","DOIUrl":null,"url":null,"abstract":"<p>Host–parasite relationships can affect the dispersal and transmission of parasites. <i>Myodopsylla insignis</i> (Rothchild, 1903), a bat flea, and <i>Spinturnix americanus</i> (Banks, 1902), a bat wing mite, are two common ectoparasites of the little brown myotis (<i>Myotis lucifugus,</i> Le Conte 1831) that differ in life cycles and time spent on the host. Our goal was to compare how life history traits and host–parasite relationships influence the genetic structure and biogeography of co-infecting ectoparasites using <i>S. americanus</i> mites and <i>M. insignis</i> fleas that feed on <i>Myotis lucifugus</i> bats. Ectoparasites were collected from bats captured at maternity roosts between 2010 and 2017 in Atlantic Canada and sequenced for the cytochrome oxidase c subunit 1 gene. We barcoded 223 <i>S. americanus</i> and 87 <i>M. insignis</i> specimens and examined their genetic diversity, genetic structure, and biogeography. We found evidence of a weak association between geographic distance and sequence divergence between Labrador and Nova Scotia for <i>M. insignis</i> and evidence of regional differentiation between the island of Newfoundland and the mainland for <i>S. americanus</i>, similar to previous findings for <i>M. lucifugus</i>. In terms of biogeography, <i>M. insignis</i> likely underwent historical population expansion, particularly in Labrador, whereas <i>S. americanus</i> may have undergone historical population expansion or selection. Our study highlights how host–parasite relationships are influenced at multiple scales by both host and parasite biology and how an understanding of both host and parasite informs predictions on how these dynamics will be affected by disturbances.</p>","PeriodicalId":11467,"journal":{"name":"Ecology and Evolution","volume":"15 4","pages":""},"PeriodicalIF":2.3000,"publicationDate":"2025-04-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/ece3.71233","citationCount":"0","resultStr":"{\"title\":\"Host–Parasite Association Dynamics Influence Dispersal and Population Genetics of Little Brown Myotis (Myotis lucifugus, Le Conte 1831) Ectoparasites\",\"authors\":\"Alexandra H. Sauk, Hugh G. Broders\",\"doi\":\"10.1002/ece3.71233\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Host–parasite relationships can affect the dispersal and transmission of parasites. <i>Myodopsylla insignis</i> (Rothchild, 1903), a bat flea, and <i>Spinturnix americanus</i> (Banks, 1902), a bat wing mite, are two common ectoparasites of the little brown myotis (<i>Myotis lucifugus,</i> Le Conte 1831) that differ in life cycles and time spent on the host. Our goal was to compare how life history traits and host–parasite relationships influence the genetic structure and biogeography of co-infecting ectoparasites using <i>S. americanus</i> mites and <i>M. insignis</i> fleas that feed on <i>Myotis lucifugus</i> bats. Ectoparasites were collected from bats captured at maternity roosts between 2010 and 2017 in Atlantic Canada and sequenced for the cytochrome oxidase c subunit 1 gene. We barcoded 223 <i>S. americanus</i> and 87 <i>M. insignis</i> specimens and examined their genetic diversity, genetic structure, and biogeography. We found evidence of a weak association between geographic distance and sequence divergence between Labrador and Nova Scotia for <i>M. insignis</i> and evidence of regional differentiation between the island of Newfoundland and the mainland for <i>S. americanus</i>, similar to previous findings for <i>M. lucifugus</i>. In terms of biogeography, <i>M. insignis</i> likely underwent historical population expansion, particularly in Labrador, whereas <i>S. americanus</i> may have undergone historical population expansion or selection. 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引用次数: 0
摘要
宿主-寄生虫关系可影响寄生虫的传播和传播。蝙蝠蚤Myodopsylla insignis (Rothchild, 1903)和蝙蝠翅螨Spinturnix americanus (Banks, 1902)是小褐蝇(myotis lucifugus, Le Conte 1831)的两种常见体外寄生虫,它们的生命周期和在宿主上停留的时间不同。我们的目的是比较生活史特征和寄主-寄生虫关系如何影响共同感染的外寄生虫的遗传结构和生物地理,研究对象是以lucifugus Myotis为食的美洲螨和insignis蚤。研究人员从2010年至2017年在加拿大大西洋地区的母性栖息地捕获的蝙蝠身上收集了体外寄生虫,并对细胞色素氧化酶c亚基1基因进行了测序。我们条形码223 S。美国和87年。研究了其遗传多样性、遗传结构和生物地理特征。我们发现在拉布拉多和新斯科舍省之间的地理距离和序列差异之间存在弱关联的证据,以及在纽芬兰岛和美洲大陆之间存在区域差异的证据,类似于之前在lucifugus上的发现。从生物地理学的角度来看,美洲藜可能经历了历史上的种群扩张,特别是在拉布拉多,而美洲藜可能经历了历史上的种群扩张或选择。我们的研究强调了宿主-寄生虫关系如何在多个尺度上受到宿主和寄生虫生物学的影响,以及对宿主和寄生虫的理解如何为预测这些动态将如何受到干扰的影响提供信息。
Host–Parasite Association Dynamics Influence Dispersal and Population Genetics of Little Brown Myotis (Myotis lucifugus, Le Conte 1831) Ectoparasites
Host–parasite relationships can affect the dispersal and transmission of parasites. Myodopsylla insignis (Rothchild, 1903), a bat flea, and Spinturnix americanus (Banks, 1902), a bat wing mite, are two common ectoparasites of the little brown myotis (Myotis lucifugus, Le Conte 1831) that differ in life cycles and time spent on the host. Our goal was to compare how life history traits and host–parasite relationships influence the genetic structure and biogeography of co-infecting ectoparasites using S. americanus mites and M. insignis fleas that feed on Myotis lucifugus bats. Ectoparasites were collected from bats captured at maternity roosts between 2010 and 2017 in Atlantic Canada and sequenced for the cytochrome oxidase c subunit 1 gene. We barcoded 223 S. americanus and 87 M. insignis specimens and examined their genetic diversity, genetic structure, and biogeography. We found evidence of a weak association between geographic distance and sequence divergence between Labrador and Nova Scotia for M. insignis and evidence of regional differentiation between the island of Newfoundland and the mainland for S. americanus, similar to previous findings for M. lucifugus. In terms of biogeography, M. insignis likely underwent historical population expansion, particularly in Labrador, whereas S. americanus may have undergone historical population expansion or selection. Our study highlights how host–parasite relationships are influenced at multiple scales by both host and parasite biology and how an understanding of both host and parasite informs predictions on how these dynamics will be affected by disturbances.
期刊介绍:
Ecology and Evolution is the peer reviewed journal for rapid dissemination of research in all areas of ecology, evolution and conservation science. The journal gives priority to quality research reports, theoretical or empirical, that develop our understanding of organisms and their diversity, interactions between them, and the natural environment.
Ecology and Evolution gives prompt and equal consideration to papers reporting theoretical, experimental, applied and descriptive work in terrestrial and aquatic environments. The journal will consider submissions across taxa in areas including but not limited to micro and macro ecological and evolutionary processes, characteristics of and interactions between individuals, populations, communities and the environment, physiological responses to environmental change, population genetics and phylogenetics, relatedness and kin selection, life histories, systematics and taxonomy, conservation genetics, extinction, speciation, adaption, behaviour, biodiversity, species abundance, macroecology, population and ecosystem dynamics, and conservation policy.