Cargando…

Geographical structure of endosymbiotic bacteria hosted by Bathymodiolus mussels at eastern Pacific hydrothermal vents

BACKGROUND: Chemolithoautotrophic primary production sustains dense invertebrate communities at deep-sea hydrothermal vents and hydrocarbon seeps. Symbiotic bacteria that oxidize dissolved sulfur, methane, and hydrogen gases nourish bathymodiolin mussels that thrive in these environments worldwide....

Descripción completa

Detalles Bibliográficos
Autores principales: Ho, Phuong-Thao, Park, Eunji, Hong, Soon Gyu, Kim, Eun-Hye, Kim, Kangchon, Jang, Sook-Jin, Vrijenhoek, Robert C., Won, Yong-Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5450337/
https://www.ncbi.nlm.nih.gov/pubmed/28558648
http://dx.doi.org/10.1186/s12862-017-0966-3
_version_ 1783239948149719040
author Ho, Phuong-Thao
Park, Eunji
Hong, Soon Gyu
Kim, Eun-Hye
Kim, Kangchon
Jang, Sook-Jin
Vrijenhoek, Robert C.
Won, Yong-Jin
author_facet Ho, Phuong-Thao
Park, Eunji
Hong, Soon Gyu
Kim, Eun-Hye
Kim, Kangchon
Jang, Sook-Jin
Vrijenhoek, Robert C.
Won, Yong-Jin
author_sort Ho, Phuong-Thao
collection PubMed
description BACKGROUND: Chemolithoautotrophic primary production sustains dense invertebrate communities at deep-sea hydrothermal vents and hydrocarbon seeps. Symbiotic bacteria that oxidize dissolved sulfur, methane, and hydrogen gases nourish bathymodiolin mussels that thrive in these environments worldwide. The mussel symbionts are newly acquired in each generation via infection by free-living forms. This study examined geographical subdivision of the thiotrophic endosymbionts hosted by Bathymodiolus mussels living along the eastern Pacific hydrothermal vents. High-throughput sequencing data of 16S ribosomal RNA encoding gene and fragments of six protein-coding genes of symbionts were examined in the samples collected from nine vent localities at the East Pacific Rise, Galápagos Rift, and Pacific-Antarctic Ridge. RESULTS: Both of the parapatric sister-species, B. thermophilus and B. antarcticus, hosted the same numerically dominant phylotype of thiotrophic Gammaproteobacteria. However, sequences from six protein-coding genes revealed highly divergent symbiont lineages living north and south of the Easter Microplate and hosted by these two Bathymodiolus mussel species. High heterogeneity of symbiont haplotypes among host individuals sampled from the same location suggested that stochasticity associated with initial infections was amplified as symbionts proliferated within the host individuals. The mussel species presently contact one another and hybridize along the Easter Microplate, but the northern and southern symbionts appear to be completely isolated. Vicariance associated with orogeny of the Easter Microplate region, 2.5–5.3 million years ago, may have initiated isolation of the symbiont and host populations. Estimates of synonymous substitution rates for the protein-coding bacterial genes examined in this study were 0.77–1.62%/nucleotide/million years. CONCLUSIONS: Our present study reports the most comprehensive population genetic analyses of the chemosynthetic endosymbiotic bacteria based on high-throughput genetic data and extensive geographical sampling to date, and demonstrates the role of the geographical features, the Easter Microplate and geographical distance, in the intraspecific divergence of this bacterial species along the mid-ocean ridge axes in the eastern Pacific. Altogether, our results provide insights into extrinsic and intrinsic factors affecting the dispersal and evolution of chemosynthetic symbiotic partners in the hydrothermal vents along the eastern Pacific Ocean. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12862-017-0966-3) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-5450337
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-54503372017-06-01 Geographical structure of endosymbiotic bacteria hosted by Bathymodiolus mussels at eastern Pacific hydrothermal vents Ho, Phuong-Thao Park, Eunji Hong, Soon Gyu Kim, Eun-Hye Kim, Kangchon Jang, Sook-Jin Vrijenhoek, Robert C. Won, Yong-Jin BMC Evol Biol Research Article BACKGROUND: Chemolithoautotrophic primary production sustains dense invertebrate communities at deep-sea hydrothermal vents and hydrocarbon seeps. Symbiotic bacteria that oxidize dissolved sulfur, methane, and hydrogen gases nourish bathymodiolin mussels that thrive in these environments worldwide. The mussel symbionts are newly acquired in each generation via infection by free-living forms. This study examined geographical subdivision of the thiotrophic endosymbionts hosted by Bathymodiolus mussels living along the eastern Pacific hydrothermal vents. High-throughput sequencing data of 16S ribosomal RNA encoding gene and fragments of six protein-coding genes of symbionts were examined in the samples collected from nine vent localities at the East Pacific Rise, Galápagos Rift, and Pacific-Antarctic Ridge. RESULTS: Both of the parapatric sister-species, B. thermophilus and B. antarcticus, hosted the same numerically dominant phylotype of thiotrophic Gammaproteobacteria. However, sequences from six protein-coding genes revealed highly divergent symbiont lineages living north and south of the Easter Microplate and hosted by these two Bathymodiolus mussel species. High heterogeneity of symbiont haplotypes among host individuals sampled from the same location suggested that stochasticity associated with initial infections was amplified as symbionts proliferated within the host individuals. The mussel species presently contact one another and hybridize along the Easter Microplate, but the northern and southern symbionts appear to be completely isolated. Vicariance associated with orogeny of the Easter Microplate region, 2.5–5.3 million years ago, may have initiated isolation of the symbiont and host populations. Estimates of synonymous substitution rates for the protein-coding bacterial genes examined in this study were 0.77–1.62%/nucleotide/million years. CONCLUSIONS: Our present study reports the most comprehensive population genetic analyses of the chemosynthetic endosymbiotic bacteria based on high-throughput genetic data and extensive geographical sampling to date, and demonstrates the role of the geographical features, the Easter Microplate and geographical distance, in the intraspecific divergence of this bacterial species along the mid-ocean ridge axes in the eastern Pacific. Altogether, our results provide insights into extrinsic and intrinsic factors affecting the dispersal and evolution of chemosynthetic symbiotic partners in the hydrothermal vents along the eastern Pacific Ocean. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12862-017-0966-3) contains supplementary material, which is available to authorized users. BioMed Central 2017-05-30 /pmc/articles/PMC5450337/ /pubmed/28558648 http://dx.doi.org/10.1186/s12862-017-0966-3 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Ho, Phuong-Thao
Park, Eunji
Hong, Soon Gyu
Kim, Eun-Hye
Kim, Kangchon
Jang, Sook-Jin
Vrijenhoek, Robert C.
Won, Yong-Jin
Geographical structure of endosymbiotic bacteria hosted by Bathymodiolus mussels at eastern Pacific hydrothermal vents
title Geographical structure of endosymbiotic bacteria hosted by Bathymodiolus mussels at eastern Pacific hydrothermal vents
title_full Geographical structure of endosymbiotic bacteria hosted by Bathymodiolus mussels at eastern Pacific hydrothermal vents
title_fullStr Geographical structure of endosymbiotic bacteria hosted by Bathymodiolus mussels at eastern Pacific hydrothermal vents
title_full_unstemmed Geographical structure of endosymbiotic bacteria hosted by Bathymodiolus mussels at eastern Pacific hydrothermal vents
title_short Geographical structure of endosymbiotic bacteria hosted by Bathymodiolus mussels at eastern Pacific hydrothermal vents
title_sort geographical structure of endosymbiotic bacteria hosted by bathymodiolus mussels at eastern pacific hydrothermal vents
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5450337/
https://www.ncbi.nlm.nih.gov/pubmed/28558648
http://dx.doi.org/10.1186/s12862-017-0966-3
work_keys_str_mv AT hophuongthao geographicalstructureofendosymbioticbacteriahostedbybathymodiolusmusselsateasternpacifichydrothermalvents
AT parkeunji geographicalstructureofendosymbioticbacteriahostedbybathymodiolusmusselsateasternpacifichydrothermalvents
AT hongsoongyu geographicalstructureofendosymbioticbacteriahostedbybathymodiolusmusselsateasternpacifichydrothermalvents
AT kimeunhye geographicalstructureofendosymbioticbacteriahostedbybathymodiolusmusselsateasternpacifichydrothermalvents
AT kimkangchon geographicalstructureofendosymbioticbacteriahostedbybathymodiolusmusselsateasternpacifichydrothermalvents
AT jangsookjin geographicalstructureofendosymbioticbacteriahostedbybathymodiolusmusselsateasternpacifichydrothermalvents
AT vrijenhoekrobertc geographicalstructureofendosymbioticbacteriahostedbybathymodiolusmusselsateasternpacifichydrothermalvents
AT wonyongjin geographicalstructureofendosymbioticbacteriahostedbybathymodiolusmusselsateasternpacifichydrothermalvents