Chiara Pedrazzini, Stephen A. Rehner, Hermann Strasser, Niklaus Zemp, Rolf Holderegger, Franco Widmer, Jürg Enkerli
{"title":"Beauveria brongniartii 和 Beauveria pseudobassiana 的克隆基因组种群结构:欧洲普通鸡毛虫(Melolontha melolontha L.)的病原体","authors":"Chiara Pedrazzini, Stephen A. Rehner, Hermann Strasser, Niklaus Zemp, Rolf Holderegger, Franco Widmer, Jürg Enkerli","doi":"10.1111/1462-2920.16612","DOIUrl":null,"url":null,"abstract":"<p><i>Beauveria brongniartii</i> is a fungal pathogen that infects the beetle <i>Melolontha melolontha</i>, a significant agricultural pest in Europe. While research has primarily focused on the use of <i>B. brongniartii</i> for controlling <i>M. melolontha</i>, the genomic structure of the <i>B. brongniartii</i> population remains unknown. This includes whether its structure is influenced by its interaction with <i>M. melolontha</i>, the timing of beetle-swarming flights, geographical factors, or reproductive mode. To address this, we analysed genome-wide SNPs to infer the population genomics of <i>Beauveria</i> spp., which were isolated from infected <i>M. melolontha</i> adults in an Alpine region. Surprisingly, only one-third of the isolates were identified as <i>B. brongniartii</i>, while two-thirds were distributed among cryptic taxa within <i>B. pseudobassiana</i>, a fungal species not previously recognized as a pathogen of <i>M. melolontha</i>. Given the prevalence of <i>B. pseudobassiana</i>, we conducted analyses on both species. We found no spatial or temporal genomic patterns within either species and no correlation with the population structure of <i>M. melolontha</i>, suggesting that the dispersal of the fungi is independent of the beetle. Both species exhibited clonal population structures, with <i>B. brongniartii</i> fixed for one mating type and <i>B. pseudobassiana</i> displaying both mating types. This implies that factors other than mating compatibility limit sexual reproduction. We conclude that the population genomic structure of <i>Beauveria</i> spp. is primarily influenced by predominant asexual reproduction and dispersal.</p>","PeriodicalId":11898,"journal":{"name":"Environmental microbiology","volume":"26 4","pages":""},"PeriodicalIF":4.3000,"publicationDate":"2024-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/1462-2920.16612","citationCount":"0","resultStr":"{\"title\":\"Clonal genomic population structure of Beauveria brongniartii and Beauveria pseudobassiana: Pathogens of the common European cockchafer (Melolontha melolontha L.)\",\"authors\":\"Chiara Pedrazzini, Stephen A. Rehner, Hermann Strasser, Niklaus Zemp, Rolf Holderegger, Franco Widmer, Jürg Enkerli\",\"doi\":\"10.1111/1462-2920.16612\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><i>Beauveria brongniartii</i> is a fungal pathogen that infects the beetle <i>Melolontha melolontha</i>, a significant agricultural pest in Europe. While research has primarily focused on the use of <i>B. brongniartii</i> for controlling <i>M. melolontha</i>, the genomic structure of the <i>B. brongniartii</i> population remains unknown. This includes whether its structure is influenced by its interaction with <i>M. melolontha</i>, the timing of beetle-swarming flights, geographical factors, or reproductive mode. To address this, we analysed genome-wide SNPs to infer the population genomics of <i>Beauveria</i> spp., which were isolated from infected <i>M. melolontha</i> adults in an Alpine region. Surprisingly, only one-third of the isolates were identified as <i>B. brongniartii</i>, while two-thirds were distributed among cryptic taxa within <i>B. pseudobassiana</i>, a fungal species not previously recognized as a pathogen of <i>M. melolontha</i>. Given the prevalence of <i>B. pseudobassiana</i>, we conducted analyses on both species. We found no spatial or temporal genomic patterns within either species and no correlation with the population structure of <i>M. melolontha</i>, suggesting that the dispersal of the fungi is independent of the beetle. Both species exhibited clonal population structures, with <i>B. brongniartii</i> fixed for one mating type and <i>B. pseudobassiana</i> displaying both mating types. This implies that factors other than mating compatibility limit sexual reproduction. We conclude that the population genomic structure of <i>Beauveria</i> spp. is primarily influenced by predominant asexual reproduction and dispersal.</p>\",\"PeriodicalId\":11898,\"journal\":{\"name\":\"Environmental microbiology\",\"volume\":\"26 4\",\"pages\":\"\"},\"PeriodicalIF\":4.3000,\"publicationDate\":\"2024-04-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1111/1462-2920.16612\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Environmental microbiology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1111/1462-2920.16612\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Environmental microbiology","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/1462-2920.16612","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
Clonal genomic population structure of Beauveria brongniartii and Beauveria pseudobassiana: Pathogens of the common European cockchafer (Melolontha melolontha L.)
Beauveria brongniartii is a fungal pathogen that infects the beetle Melolontha melolontha, a significant agricultural pest in Europe. While research has primarily focused on the use of B. brongniartii for controlling M. melolontha, the genomic structure of the B. brongniartii population remains unknown. This includes whether its structure is influenced by its interaction with M. melolontha, the timing of beetle-swarming flights, geographical factors, or reproductive mode. To address this, we analysed genome-wide SNPs to infer the population genomics of Beauveria spp., which were isolated from infected M. melolontha adults in an Alpine region. Surprisingly, only one-third of the isolates were identified as B. brongniartii, while two-thirds were distributed among cryptic taxa within B. pseudobassiana, a fungal species not previously recognized as a pathogen of M. melolontha. Given the prevalence of B. pseudobassiana, we conducted analyses on both species. We found no spatial or temporal genomic patterns within either species and no correlation with the population structure of M. melolontha, suggesting that the dispersal of the fungi is independent of the beetle. Both species exhibited clonal population structures, with B. brongniartii fixed for one mating type and B. pseudobassiana displaying both mating types. This implies that factors other than mating compatibility limit sexual reproduction. We conclude that the population genomic structure of Beauveria spp. is primarily influenced by predominant asexual reproduction and dispersal.
期刊介绍:
Environmental Microbiology provides a high profile vehicle for publication of the most innovative, original and rigorous research in the field. The scope of the Journal encompasses the diversity of current research on microbial processes in the environment, microbial communities, interactions and evolution and includes, but is not limited to, the following:
the structure, activities and communal behaviour of microbial communities
microbial community genetics and evolutionary processes
microbial symbioses, microbial interactions and interactions with plants, animals and abiotic factors
microbes in the tree of life, microbial diversification and evolution
population biology and clonal structure
microbial metabolic and structural diversity
microbial physiology, growth and survival
microbes and surfaces, adhesion and biofouling
responses to environmental signals and stress factors
modelling and theory development
pollution microbiology
extremophiles and life in extreme and unusual little-explored habitats
element cycles and biogeochemical processes, primary and secondary production
microbes in a changing world, microbially-influenced global changes
evolution and diversity of archaeal and bacterial viruses
new technological developments in microbial ecology and evolution, in particular for the study of activities of microbial communities, non-culturable microorganisms and emerging pathogens