ArticleGenome biology and evolution2017
Ancient Occasional Host Switching of Maternally Transmitted Bacterial Symbionts of Chemosynthetic Vesicomyid Clams.
Article in Genome biology and evolution, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.
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14 citing papers in PubMed.
- The Host-Symbiont-Pathogen Triad inMarine drugs · 2026Review
- A novel bioenergetic model outlines the metabolism of a deep-sea clam and that of its sulfur-oxidizing symbionts.Scientific reports · 2026Article
- Endosymbioses Have Shaped the Evolution of Biological Diversity and Complexity Time and Time Again.Genome biology and evolution · 2024Review
- Early genome erosion and internal phage-symbiont-host interaction in the endosymbionts of a cold-seep tubeworm.iScience · 2023Article
- Endosymbiont population genomics sheds light on transmission mode, partner specificity, and stability of the scaly-foot snail holobiont.The ISME journal · 2022Article
- Symbiont Community Composition inApplied and environmental microbiology · 2022Article
- Divergent paths in the evolutionary history of maternally transmitted clam symbionts.Proceedings. Biological sciences · 2022Article
- Host-Endosymbiont Genome Integration in a Deep-Sea Chemosymbiotic Clam.Molecular biology and evolution · 2021Article
- Horizontal transmission and recombination maintain forever young bacterial symbiont genomes.PLoS genetics · 2020Article
- Host hybridization as a potential mechanism of lateral symbiont transfer in deep-sea vesicomyid clams.Molecular ecology · 2019Article
- Match and mismatch between dietary switches and microbial partners in plant sap-feeding insects.Proceedings. Biological sciences · 2019Article
- Article
- Transmission strategies in a chemosynthetic symbiosis: detection and quantification of symbionts in host tissues and their environment.Proceedings. Biological sciences · 2018Article
- Comparative mitochondrial genomic analyses of three chemosynthetic vesicomyid clams from deep-sea habitats.Ecology and evolution · 2018Article
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9 authors.
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Abstract
Vesicomyid clams in deep-sea chemosynthetic ecosystems harbor sulfur-oxidizing bacteria in their gill epithelial cells. These symbionts, which are vertically transmitted, are species-specific and thought to have cospeciated with their hosts. However, recent studies indicate incongruent phylogenies between some vesicomyid clams and their symbionts, suggesting that symbionts are horizontally transmitted. To more precisely understand the evolution of vesicomyid clams and their symbionts, we compared the evolution of vesicomyid clams and their symbionts through phylogenetic analyses using multi-gene data sets. Many clades in the phylogenetic trees of 13 host species (Abyssogena mariana, Ab. phaseoliformis, Akebiconcha kawamurai, Calyptogena fausta, C. laubieri, C. magnifica, C. nautilei, C. pacifica, Isorropodon fossajaponicum, Phreagena kilmeri, Ph. okutanii, Ph. soyoae, and Pliocardia stearnsii) and their symbionts were well resolved. Six of the 13 host-symbiont pairs (C. fausta, C. magnifica, C. pacifica, Ph. kilmeri, Ph. okutanii, and Ph. soyoae, and their respective symbionts) showed topological congruence. However, the remaining seven pairs (Ak. kawamurai, Ab mariana, Ab. phaseoliformis, C. laubieri, C. nautilei, I. fossajaponicum, and Pl. stearnsii and their corresponding symbionts) showed incongruent topologies, which were supported by the approximately unbiased and Bayes factor tests. Coevolution analyses indicated that six pairs cospeciated, whereas host switching events occurred in the remaining seven pairs. Markedly, multiple host switching events may have occurred in the lineages from the common ancestral symbiont of C. pacifica and C. fausta. Our phylogenetic and coevolution analyses provide additional evidence for host switching during the evolution of vesicomyids.
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