{"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. 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":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Ecology and Evolution","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/ece3.71233","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ECOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
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.