» Articles » PMID: 23091033

Evidence for the Role of Endosymbionts in Regional-scale Habitat Partitioning by Hydrothermal Vent Symbioses

Overview
Specialty Science
Date 2012 Oct 24
PMID 23091033
Citations 37
Authors
Affiliations
Soon will be listed here.
Abstract

Deep-sea hydrothermal vents are populated by dense communities of animals that form symbiotic associations with chemolithoautotrophic bacteria. To date, our understanding of which factors govern the distribution of host/symbiont associations (or holobionts) in nature is limited, although host physiology often is invoked. In general, the role that symbionts play in habitat utilization by vent holobionts has not been thoroughly addressed. Here we present evidence for symbiont-influenced, regional-scale niche partitioning among symbiotic gastropods (genus Alviniconcha) in the Lau Basin. We extensively surveyed Alviniconcha holobionts from four vent fields using quantitative molecular approaches, coupled to characterization of high-temperature and diffuse vent-fluid composition using gastight samplers and in situ electrochemical analyses, respectively. Phylogenetic analyses exposed cryptic host and symbiont diversity, revealing three distinct host types and three different symbiont phylotypes (one ε-proteobacteria and two γ-proteobacteria) that formed specific associations with one another. Strikingly, we observed that holobionts with ε-proteobacterial symbionts were dominant at the northern fields, whereas holobionts with γ-proteobacterial symbionts were dominant in the southern fields. This pattern of distribution corresponds to differences in the vent geochemistry that result from deep subsurface geological and geothermal processes. We posit that the symbionts, likely through differences in chemolithoautotrophic metabolism, influence niche utilization among these holobionts. The data presented here represent evidence linking symbiont type to habitat partitioning among the chemosynthetic symbioses at hydrothermal vents and illustrate the coupling between subsurface geothermal processes and niche availability.

Citing Articles

Stochasticity, determinism, and contingency shape genome evolution of endosymbiotic bacteria.

Boyd B, James I, Johnson K, Weiss R, Bush S, Clayton D Nat Commun. 2024; 15(1):4571.

PMID: 38811551 PMC: 11137140. DOI: 10.1038/s41467-024-48784-2.


Mosaic environment-driven evolution of the deep-sea mussel Gigantidas platifrons bacterial endosymbiont.

Sun Y, Wang M, Cao L, Seim I, Zhou L, Chen J Microbiome. 2023; 11(1):253.

PMID: 37974296 PMC: 10652631. DOI: 10.1186/s40168-023-01695-8.


Symbioses of alvinocaridid shrimps from the South West Pacific: No chemosymbiotic diets but conserved gut microbiomes.

Methou P, Cueff-Gauchard V, Michel L, Gayet N, Pradillon F, Cambon-Bonavita M Environ Microbiol Rep. 2023; 15(6):614-630.

PMID: 37752716 PMC: 10667644. DOI: 10.1111/1758-2229.13201.


Ecological differences among hydrothermal vent symbioses may drive contrasting patterns of symbiont population differentiation.

Breusing C, Xiao Y, Russell S, Corbett-Detig R, Li S, Sun J mSystems. 2023; 8(4):e0028423.

PMID: 37493648 PMC: 10469979. DOI: 10.1128/msystems.00284-23.


Geography, not lifestyle, explains the population structure of free-living and host-associated deep-sea hydrothermal vent snail symbionts.

Hauer M, Breusing C, Trembath-Reichert E, Huber J, Beinart R Microbiome. 2023; 11(1):106.

PMID: 37189129 PMC: 10186799. DOI: 10.1186/s40168-023-01493-2.


References
1.
Hsu-Kim H, Mullaugh K, Tsang J, Yucel M, Luther 3rd G . Formation of Zn- and Fe-sulfides near hydrothermal vents at the Eastern Lau Spreading Center: implications for sulfide bioavailability to chemoautotrophs. Geochem Trans. 2008; 9:6. PMC: 2396607. DOI: 10.1186/1467-4866-9-6. View

2.
Finney J, Pettay D, Sampayo E, Warner M, Oxenford H, LaJeunesse T . The relative significance of host-habitat, depth, and geography on the ecology, endemism, and speciation of coral endosymbionts in the genus Symbiodinium. Microb Ecol. 2010; 60(1):250-63. DOI: 10.1007/s00248-010-9681-y. View

3.
Drummond A, Rambaut A . BEAST: Bayesian evolutionary analysis by sampling trees. BMC Evol Biol. 2007; 7:214. PMC: 2247476. DOI: 10.1186/1471-2148-7-214. View

4.
Felbeck H . Chemoautotrophic Potential of the Hydrothermal Vent Tube Worm, Riftia pachyptila Jones (Vestimentifera). Science. 1981; 213(4505):336-8. DOI: 10.1126/science.213.4505.336. View

5.
Leibold M, McPeek M . Coexistence of the niche and neutral perspectives in community ecology. Ecology. 2006; 87(6):1399-410. DOI: 10.1890/0012-9658(2006)87[1399:cotnan]2.0.co;2. View