Juliana Soto-Patiño, Kimberly K O Walden, Jorge Doña, Lorenzo Mario D'Alessio, Sarah E Bush, Dale H Clayton, Colin Dale, Kevin P Johnson
{"title":"独立和反复获取的Sodalis内共生细菌跨越羽毛虱的多样化。","authors":"Juliana Soto-Patiño, Kimberly K O Walden, Jorge Doña, Lorenzo Mario D'Alessio, Sarah E Bush, Dale H Clayton, Colin Dale, Kevin P Johnson","doi":"10.1098/rsos.251220","DOIUrl":null,"url":null,"abstract":"<p><p>Many parasitic insects, including lice, form close relationships with endosymbiotic bacteria that are crucial for their survival. In this study, we used genomic sequencing to investigate the distribution and evolutionary history of the bacterial genus <i>Sodalis</i> across a broad range of feather louse species spanning 140 genera. Phylogenomic analysis revealed significant diversity among <i>Sodalis</i> lineages in feather lice and robust evidence for their independent and repeated acquisition by different louse clades throughout their radiation. Among the 1020 louse genomes analysed, at least 22% contained <i>Sodalis</i>, distributed across 57 louse genera. Cophylogenetic analyses between the <i>Sodalis</i> and feather louse phylogenies indicated considerable mismatch. This phylogenetic incongruence between lice and <i>Sodalis</i>, along with the presence of distantly related <i>Sodalis</i> lineages in otherwise closely related louse species, strongly indicates repeated independent acquisition of this endosymbiont. Additionally, evidence of cospeciation among a few closely related louse species, coupled with frequent acquisition of these endosymbionts from free-living bacteria, further highlights the diverse evolutionary processes shaping <i>Sodalis</i> endosymbiosis in feather lice.</p>","PeriodicalId":21525,"journal":{"name":"Royal Society Open Science","volume":"12 9","pages":"251220"},"PeriodicalIF":2.9000,"publicationDate":"2025-09-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12441319/pdf/","citationCount":"0","resultStr":"{\"title\":\"Independent and repeated acquisition of <i>Sodalis</i> endosymbiotic bacteria across the diversification of feather lice.\",\"authors\":\"Juliana Soto-Patiño, Kimberly K O Walden, Jorge Doña, Lorenzo Mario D'Alessio, Sarah E Bush, Dale H Clayton, Colin Dale, Kevin P Johnson\",\"doi\":\"10.1098/rsos.251220\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Many parasitic insects, including lice, form close relationships with endosymbiotic bacteria that are crucial for their survival. In this study, we used genomic sequencing to investigate the distribution and evolutionary history of the bacterial genus <i>Sodalis</i> across a broad range of feather louse species spanning 140 genera. Phylogenomic analysis revealed significant diversity among <i>Sodalis</i> lineages in feather lice and robust evidence for their independent and repeated acquisition by different louse clades throughout their radiation. Among the 1020 louse genomes analysed, at least 22% contained <i>Sodalis</i>, distributed across 57 louse genera. Cophylogenetic analyses between the <i>Sodalis</i> and feather louse phylogenies indicated considerable mismatch. This phylogenetic incongruence between lice and <i>Sodalis</i>, along with the presence of distantly related <i>Sodalis</i> lineages in otherwise closely related louse species, strongly indicates repeated independent acquisition of this endosymbiont. Additionally, evidence of cospeciation among a few closely related louse species, coupled with frequent acquisition of these endosymbionts from free-living bacteria, further highlights the diverse evolutionary processes shaping <i>Sodalis</i> endosymbiosis in feather lice.</p>\",\"PeriodicalId\":21525,\"journal\":{\"name\":\"Royal Society Open Science\",\"volume\":\"12 9\",\"pages\":\"251220\"},\"PeriodicalIF\":2.9000,\"publicationDate\":\"2025-09-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12441319/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Royal Society Open Science\",\"FirstCategoryId\":\"103\",\"ListUrlMain\":\"https://doi.org/10.1098/rsos.251220\",\"RegionNum\":3,\"RegionCategory\":\"综合性期刊\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/9/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q1\",\"JCRName\":\"MULTIDISCIPLINARY SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Royal Society Open Science","FirstCategoryId":"103","ListUrlMain":"https://doi.org/10.1098/rsos.251220","RegionNum":3,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/9/1 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
Independent and repeated acquisition of Sodalis endosymbiotic bacteria across the diversification of feather lice.
Many parasitic insects, including lice, form close relationships with endosymbiotic bacteria that are crucial for their survival. In this study, we used genomic sequencing to investigate the distribution and evolutionary history of the bacterial genus Sodalis across a broad range of feather louse species spanning 140 genera. Phylogenomic analysis revealed significant diversity among Sodalis lineages in feather lice and robust evidence for their independent and repeated acquisition by different louse clades throughout their radiation. Among the 1020 louse genomes analysed, at least 22% contained Sodalis, distributed across 57 louse genera. Cophylogenetic analyses between the Sodalis and feather louse phylogenies indicated considerable mismatch. This phylogenetic incongruence between lice and Sodalis, along with the presence of distantly related Sodalis lineages in otherwise closely related louse species, strongly indicates repeated independent acquisition of this endosymbiont. Additionally, evidence of cospeciation among a few closely related louse species, coupled with frequent acquisition of these endosymbionts from free-living bacteria, further highlights the diverse evolutionary processes shaping Sodalis endosymbiosis in feather lice.
期刊介绍:
Royal Society Open Science is a new open journal publishing high-quality original research across the entire range of science on the basis of objective peer-review.
The journal covers the entire range of science and mathematics and will allow the Society to publish all the high-quality work it receives without the usual restrictions on scope, length or impact.