{"title":"Phylogenetic history of the acquisition of molluscan hosts in acotylean flatworms.","authors":"Osamu Kagawa, Hajime Itoh, Nobuyoshi Nakajima, Hiroaki Fukumori","doi":"10.1098/rsbl.2024.0721","DOIUrl":null,"url":null,"abstract":"<p><p>How symbionts acquired hosts and diversified phylogenetically during their evolutionary history is a focus of attention in many symbiotic taxa. Marine polyclad flatworms are usually free-living, but some are symbiotic, using animals as hosts. However, the history of their acquisition of symbiotic systems is not well understood. Therefore, we focused on mollusc symbiotic flatworms in the suborder Acotylea and investigated the host specificity and phylogenetic history of the acquisition of symbiosis. Field surveys revealed that symbiotic flatworms utilized certain molluscs as hosts. In particular, <i>Stylochoplana pusilla</i> and <i>Stylochoplana parasitica</i> utilized different molluscan species as hosts sympatrically. The phylogenetic analysis and the ancestral state reconstruction indicate that the mollusc symbiotic flatworms formed a monophyletic group and that their common ancestor shifted from free-living to mollusc symbiosis. These results suggest that each of the flatworms did not independently acquire a symbiotic system with molluscan hosts during its phylogenetic history, but that their common ancestor acquired a mollusc symbiotic system, which then underwent acquisition of host specificity and speciation. This study emphasizes that multiple host use can be a driving force for niche advancement and speciation in the symbionts.</p>","PeriodicalId":9005,"journal":{"name":"Biology Letters","volume":"21 4","pages":"20240721"},"PeriodicalIF":2.8000,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biology Letters","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1098/rsbl.2024.0721","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/4/9 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
How symbionts acquired hosts and diversified phylogenetically during their evolutionary history is a focus of attention in many symbiotic taxa. Marine polyclad flatworms are usually free-living, but some are symbiotic, using animals as hosts. However, the history of their acquisition of symbiotic systems is not well understood. Therefore, we focused on mollusc symbiotic flatworms in the suborder Acotylea and investigated the host specificity and phylogenetic history of the acquisition of symbiosis. Field surveys revealed that symbiotic flatworms utilized certain molluscs as hosts. In particular, Stylochoplana pusilla and Stylochoplana parasitica utilized different molluscan species as hosts sympatrically. The phylogenetic analysis and the ancestral state reconstruction indicate that the mollusc symbiotic flatworms formed a monophyletic group and that their common ancestor shifted from free-living to mollusc symbiosis. These results suggest that each of the flatworms did not independently acquire a symbiotic system with molluscan hosts during its phylogenetic history, but that their common ancestor acquired a mollusc symbiotic system, which then underwent acquisition of host specificity and speciation. This study emphasizes that multiple host use can be a driving force for niche advancement and speciation in the symbionts.
期刊介绍:
Previously a supplement to Proceedings B, and launched as an independent journal in 2005, Biology Letters is a primarily online, peer-reviewed journal that publishes short, high-quality articles, reviews and opinion pieces from across the biological sciences. The scope of Biology Letters is vast - publishing high-quality research in any area of the biological sciences. However, we have particular strengths in the biology, evolution and ecology of whole organisms. We also publish in other areas of biology, such as molecular ecology and evolution, environmental science, and phylogenetics.