{"title":"How Population Structure and Nest Membership Shape Pathogen Patterns in Bumble Bees.","authors":"Jana Dobelmann, Lena Wilfert","doi":"10.1111/mec.70146","DOIUrl":null,"url":null,"abstract":"<p><p>Host density, genetic diversity and social groups are key factors influencing pathogen transmission in wildlife populations, but their interactions remain poorly understood in insects. Islands can provide natural laboratories with distinct populations that vary in density and genetic diversity, whereby dense, genetically homogeneous populations are expected to facilitate pathogen transmission. We used bumble bees to test these predictions, assessing the population structure of the two common species Bombus pascuorum and B. terrestris across island and mainland sites in the British Isles and France and testing bees for five micro-parasitic and four viral pathogens. B. pascuorum formed distinct genetic clusters on islands, with varying levels of heterozygosity and only the Isle of Arran clustered with mainland populations. B. terrestris populations were less structured, but populations on the Isle of Man and the Scilly Isles were genetically separated from other island and mainland populations while showing low heterozygosity. Colony density was similar between species and not linked to genetic diversity but had a positive effect on the prevalence of some pathogens. Contrary to expectations, there was no protective effect of high genetic diversity, suggesting that generalist bumble bee pathogens could be more affected by host species diversity and density. Yet, within B. terrestris populations, we found that nestmates showed more similar pathogen profiles than unrelated individuals, suggesting that genetic similarity and high contact rates within nests affect pathogen prevalence in wild bees.</p>","PeriodicalId":210,"journal":{"name":"Molecular Ecology","volume":" ","pages":"e70146"},"PeriodicalIF":3.9000,"publicationDate":"2025-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Ecology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1111/mec.70146","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Host density, genetic diversity and social groups are key factors influencing pathogen transmission in wildlife populations, but their interactions remain poorly understood in insects. Islands can provide natural laboratories with distinct populations that vary in density and genetic diversity, whereby dense, genetically homogeneous populations are expected to facilitate pathogen transmission. We used bumble bees to test these predictions, assessing the population structure of the two common species Bombus pascuorum and B. terrestris across island and mainland sites in the British Isles and France and testing bees for five micro-parasitic and four viral pathogens. B. pascuorum formed distinct genetic clusters on islands, with varying levels of heterozygosity and only the Isle of Arran clustered with mainland populations. B. terrestris populations were less structured, but populations on the Isle of Man and the Scilly Isles were genetically separated from other island and mainland populations while showing low heterozygosity. Colony density was similar between species and not linked to genetic diversity but had a positive effect on the prevalence of some pathogens. Contrary to expectations, there was no protective effect of high genetic diversity, suggesting that generalist bumble bee pathogens could be more affected by host species diversity and density. Yet, within B. terrestris populations, we found that nestmates showed more similar pathogen profiles than unrelated individuals, suggesting that genetic similarity and high contact rates within nests affect pathogen prevalence in wild bees.
期刊介绍:
Molecular Ecology publishes papers that utilize molecular genetic techniques to address consequential questions in ecology, evolution, behaviour and conservation. Studies may employ neutral markers for inference about ecological and evolutionary processes or examine ecologically important genes and their products directly. We discourage papers that are primarily descriptive and are relevant only to the taxon being studied. Papers reporting on molecular marker development, molecular diagnostics, barcoding, or DNA taxonomy, or technical methods should be re-directed to our sister journal, Molecular Ecology Resources. Likewise, papers with a strongly applied focus should be submitted to Evolutionary Applications. Research areas of interest to Molecular Ecology include:
* population structure and phylogeography
* reproductive strategies
* relatedness and kin selection
* sex allocation
* population genetic theory
* analytical methods development
* conservation genetics
* speciation genetics
* microbial biodiversity
* evolutionary dynamics of QTLs
* ecological interactions
* molecular adaptation and environmental genomics
* impact of genetically modified organisms