Cargando…

Cryptic diversity and spatial genetic variation in the coral Acropora tenuis and its endosymbionts across the Great Barrier Reef

Genomic studies are uncovering extensive cryptic diversity within reef‐building corals, suggesting that evolutionarily and ecologically relevant diversity is highly underestimated in the very organisms that structure coral reefs. Furthermore, endosymbiotic algae within coral host species can confer...

Descripción completa

Detalles Bibliográficos
Autores principales: Matias, Ambrocio Melvin A., Popovic, Iva, Thia, Joshua A., Cooke, Ira R., Torda, Gergely, Lukoschek, Vimoksalehi, Bay, Line K., Kim, Sun W., Riginos, Cynthia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9923489/
https://www.ncbi.nlm.nih.gov/pubmed/36793689
http://dx.doi.org/10.1111/eva.13435
_version_ 1784887752110637056
author Matias, Ambrocio Melvin A.
Popovic, Iva
Thia, Joshua A.
Cooke, Ira R.
Torda, Gergely
Lukoschek, Vimoksalehi
Bay, Line K.
Kim, Sun W.
Riginos, Cynthia
author_facet Matias, Ambrocio Melvin A.
Popovic, Iva
Thia, Joshua A.
Cooke, Ira R.
Torda, Gergely
Lukoschek, Vimoksalehi
Bay, Line K.
Kim, Sun W.
Riginos, Cynthia
author_sort Matias, Ambrocio Melvin A.
collection PubMed
description Genomic studies are uncovering extensive cryptic diversity within reef‐building corals, suggesting that evolutionarily and ecologically relevant diversity is highly underestimated in the very organisms that structure coral reefs. Furthermore, endosymbiotic algae within coral host species can confer adaptive responses to environmental stress and may represent additional axes of coral genetic variation that are not constrained by taxonomic divergence of the cnidarian host. Here, we examine genetic variation in a common and widespread, reef‐building coral, Acropora tenuis, and its associated endosymbiotic algae along the entire expanse of the Great Barrier Reef (GBR). We use SNPs derived from genome‐wide sequencing to characterize the cnidarian coral host and organelles from zooxanthellate endosymbionts (genus Cladocopium). We discover three distinct and sympatric genetic clusters of coral hosts, whose distributions appear associated with latitude and inshore–offshore reef position. Demographic modelling suggests that the divergence history of the three distinct host taxa ranges from 0.5 to 1.5 million years ago, preceding the GBR's formation, and has been characterized by low‐to‐moderate ongoing inter‐taxon gene flow, consistent with occasional hybridization and introgression typifying coral evolution. Despite this differentiation in the cnidarian host, A. tenuis taxa share a common symbiont pool, dominated by the genus Cladocopium (Clade C). Cladocopium plastid diversity is not strongly associated with host identity but varies with reef location relative to shore: inshore colonies contain lower symbiont diversity on average but have greater differences between colonies as compared with symbiont communities from offshore colonies. Spatial genetic patterns of symbiont communities could reflect local selective pressures maintaining coral holobiont differentiation across an inshore–offshore environmental gradient. The strong influence of environment (but not host identity) on symbiont community composition supports the notion that symbiont community composition responds to habitat and may assist in the adaptation of corals to future environmental change.
format Online
Article
Text
id pubmed-9923489
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-99234892023-02-14 Cryptic diversity and spatial genetic variation in the coral Acropora tenuis and its endosymbionts across the Great Barrier Reef Matias, Ambrocio Melvin A. Popovic, Iva Thia, Joshua A. Cooke, Ira R. Torda, Gergely Lukoschek, Vimoksalehi Bay, Line K. Kim, Sun W. Riginos, Cynthia Evol Appl Special Issue Articles Genomic studies are uncovering extensive cryptic diversity within reef‐building corals, suggesting that evolutionarily and ecologically relevant diversity is highly underestimated in the very organisms that structure coral reefs. Furthermore, endosymbiotic algae within coral host species can confer adaptive responses to environmental stress and may represent additional axes of coral genetic variation that are not constrained by taxonomic divergence of the cnidarian host. Here, we examine genetic variation in a common and widespread, reef‐building coral, Acropora tenuis, and its associated endosymbiotic algae along the entire expanse of the Great Barrier Reef (GBR). We use SNPs derived from genome‐wide sequencing to characterize the cnidarian coral host and organelles from zooxanthellate endosymbionts (genus Cladocopium). We discover three distinct and sympatric genetic clusters of coral hosts, whose distributions appear associated with latitude and inshore–offshore reef position. Demographic modelling suggests that the divergence history of the three distinct host taxa ranges from 0.5 to 1.5 million years ago, preceding the GBR's formation, and has been characterized by low‐to‐moderate ongoing inter‐taxon gene flow, consistent with occasional hybridization and introgression typifying coral evolution. Despite this differentiation in the cnidarian host, A. tenuis taxa share a common symbiont pool, dominated by the genus Cladocopium (Clade C). Cladocopium plastid diversity is not strongly associated with host identity but varies with reef location relative to shore: inshore colonies contain lower symbiont diversity on average but have greater differences between colonies as compared with symbiont communities from offshore colonies. Spatial genetic patterns of symbiont communities could reflect local selective pressures maintaining coral holobiont differentiation across an inshore–offshore environmental gradient. The strong influence of environment (but not host identity) on symbiont community composition supports the notion that symbiont community composition responds to habitat and may assist in the adaptation of corals to future environmental change. John Wiley and Sons Inc. 2022-07-07 /pmc/articles/PMC9923489/ /pubmed/36793689 http://dx.doi.org/10.1111/eva.13435 Text en © 2022 The Authors. Evolutionary Applications published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Special Issue Articles
Matias, Ambrocio Melvin A.
Popovic, Iva
Thia, Joshua A.
Cooke, Ira R.
Torda, Gergely
Lukoschek, Vimoksalehi
Bay, Line K.
Kim, Sun W.
Riginos, Cynthia
Cryptic diversity and spatial genetic variation in the coral Acropora tenuis and its endosymbionts across the Great Barrier Reef
title Cryptic diversity and spatial genetic variation in the coral Acropora tenuis and its endosymbionts across the Great Barrier Reef
title_full Cryptic diversity and spatial genetic variation in the coral Acropora tenuis and its endosymbionts across the Great Barrier Reef
title_fullStr Cryptic diversity and spatial genetic variation in the coral Acropora tenuis and its endosymbionts across the Great Barrier Reef
title_full_unstemmed Cryptic diversity and spatial genetic variation in the coral Acropora tenuis and its endosymbionts across the Great Barrier Reef
title_short Cryptic diversity and spatial genetic variation in the coral Acropora tenuis and its endosymbionts across the Great Barrier Reef
title_sort cryptic diversity and spatial genetic variation in the coral acropora tenuis and its endosymbionts across the great barrier reef
topic Special Issue Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9923489/
https://www.ncbi.nlm.nih.gov/pubmed/36793689
http://dx.doi.org/10.1111/eva.13435
work_keys_str_mv AT matiasambrociomelvina crypticdiversityandspatialgeneticvariationinthecoralacroporatenuisanditsendosymbiontsacrossthegreatbarrierreef
AT popoviciva crypticdiversityandspatialgeneticvariationinthecoralacroporatenuisanditsendosymbiontsacrossthegreatbarrierreef
AT thiajoshuaa crypticdiversityandspatialgeneticvariationinthecoralacroporatenuisanditsendosymbiontsacrossthegreatbarrierreef
AT cookeirar crypticdiversityandspatialgeneticvariationinthecoralacroporatenuisanditsendosymbiontsacrossthegreatbarrierreef
AT tordagergely crypticdiversityandspatialgeneticvariationinthecoralacroporatenuisanditsendosymbiontsacrossthegreatbarrierreef
AT lukoschekvimoksalehi crypticdiversityandspatialgeneticvariationinthecoralacroporatenuisanditsendosymbiontsacrossthegreatbarrierreef
AT baylinek crypticdiversityandspatialgeneticvariationinthecoralacroporatenuisanditsendosymbiontsacrossthegreatbarrierreef
AT kimsunw crypticdiversityandspatialgeneticvariationinthecoralacroporatenuisanditsendosymbiontsacrossthegreatbarrierreef
AT riginoscynthia crypticdiversityandspatialgeneticvariationinthecoralacroporatenuisanditsendosymbiontsacrossthegreatbarrierreef