Untangling the molecular basis of coral response to sedimentation

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Untangling the molecular basis of coral response to sedimentation. / Bollati, Elena; Rosenberg, Yaeli; Simon-Blecher, Noa; Tamir, Raz; Levy, Oren; Huang, Danwei.

In: Molecular Ecology, Vol. 31, No. 3, 2022, p. 884-901.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Bollati, E, Rosenberg, Y, Simon-Blecher, N, Tamir, R, Levy, O & Huang, D 2022, 'Untangling the molecular basis of coral response to sedimentation', Molecular Ecology, vol. 31, no. 3, pp. 884-901. https://doi.org/10.1111/mec.16263

APA

Bollati, E., Rosenberg, Y., Simon-Blecher, N., Tamir, R., Levy, O., & Huang, D. (2022). Untangling the molecular basis of coral response to sedimentation. Molecular Ecology, 31(3), 884-901. https://doi.org/10.1111/mec.16263

Vancouver

Bollati E, Rosenberg Y, Simon-Blecher N, Tamir R, Levy O, Huang D. Untangling the molecular basis of coral response to sedimentation. Molecular Ecology. 2022;31(3):884-901. https://doi.org/10.1111/mec.16263

Author

Bollati, Elena ; Rosenberg, Yaeli ; Simon-Blecher, Noa ; Tamir, Raz ; Levy, Oren ; Huang, Danwei. / Untangling the molecular basis of coral response to sedimentation. In: Molecular Ecology. 2022 ; Vol. 31, No. 3. pp. 884-901.

Bibtex

@article{48bfb04f1d724726bc3ab6f75b187350,
title = "Untangling the molecular basis of coral response to sedimentation",
abstract = "Urbanized coral reefs are often chronically affected by sedimentation and reduced light levels, yet many species of corals appear to be able to thrive under these highly disturbed conditions. Recently, these marginal ecosystems have gained attention as potential climate change refugia due to the shading effect of suspended sediment, as well as potential reservoirs for stress-tolerant species. However, little research exists on the impact of sedimentation on coral physiology, particularly at the molecular level. Here, we investigated the transcriptomic response to sediment stress in corals of the family Merulinidae from a chronically turbid reef (one genet each of Goniastrea pectinata and Mycedium elephantotus from Singapore) and a clear-water reef (multiple genets of G. pectinata from the Gulf of Aqaba/Eilat). In two ex-situ experiments, we exposed corals to either natural sediment or artificial sediment enriched with organic matter and used whole-transcriptome sequencing (RNA sequencing) to quantify gene expression. Analysis revealed a shared basis for the coral transcriptomic response to sediment stress, which involves the expression of genes broadly related to energy metabolism and immune response. In particular, sediment exposure induced upregulation of anaerobic glycolysis and glyoxylate bypass enzymes, as well as genes involved in hydrogen sulphide metabolism and in pathogen pattern recognition. Our results point towards hypoxia as a probable driver of this transcriptomic response, providing a molecular basis to previous work that identified hypoxia as a primary cause of tissue necrosis in sediment-stressed corals. Potential metabolic and immunity trade-offs of corals living under chronic sedimentation should be considered in future studies on the ecology and conservation of turbid reefs.",
keywords = "Indo-Pacific, marginal reefs, Scleractinia, transcriptomics, turbid reefs, urbanization",
author = "Elena Bollati and Yaeli Rosenberg and Noa Simon-Blecher and Raz Tamir and Oren Levy and Danwei Huang",
note = "Publisher Copyright: {\textcopyright} 2021 John Wiley & Sons Ltd",
year = "2022",
doi = "10.1111/mec.16263",
language = "English",
volume = "31",
pages = "884--901",
journal = "Molecular Ecology",
issn = "0962-1083",
publisher = "Wiley-Blackwell",
number = "3",

}

RIS

TY - JOUR

T1 - Untangling the molecular basis of coral response to sedimentation

AU - Bollati, Elena

AU - Rosenberg, Yaeli

AU - Simon-Blecher, Noa

AU - Tamir, Raz

AU - Levy, Oren

AU - Huang, Danwei

N1 - Publisher Copyright: © 2021 John Wiley & Sons Ltd

PY - 2022

Y1 - 2022

N2 - Urbanized coral reefs are often chronically affected by sedimentation and reduced light levels, yet many species of corals appear to be able to thrive under these highly disturbed conditions. Recently, these marginal ecosystems have gained attention as potential climate change refugia due to the shading effect of suspended sediment, as well as potential reservoirs for stress-tolerant species. However, little research exists on the impact of sedimentation on coral physiology, particularly at the molecular level. Here, we investigated the transcriptomic response to sediment stress in corals of the family Merulinidae from a chronically turbid reef (one genet each of Goniastrea pectinata and Mycedium elephantotus from Singapore) and a clear-water reef (multiple genets of G. pectinata from the Gulf of Aqaba/Eilat). In two ex-situ experiments, we exposed corals to either natural sediment or artificial sediment enriched with organic matter and used whole-transcriptome sequencing (RNA sequencing) to quantify gene expression. Analysis revealed a shared basis for the coral transcriptomic response to sediment stress, which involves the expression of genes broadly related to energy metabolism and immune response. In particular, sediment exposure induced upregulation of anaerobic glycolysis and glyoxylate bypass enzymes, as well as genes involved in hydrogen sulphide metabolism and in pathogen pattern recognition. Our results point towards hypoxia as a probable driver of this transcriptomic response, providing a molecular basis to previous work that identified hypoxia as a primary cause of tissue necrosis in sediment-stressed corals. Potential metabolic and immunity trade-offs of corals living under chronic sedimentation should be considered in future studies on the ecology and conservation of turbid reefs.

AB - Urbanized coral reefs are often chronically affected by sedimentation and reduced light levels, yet many species of corals appear to be able to thrive under these highly disturbed conditions. Recently, these marginal ecosystems have gained attention as potential climate change refugia due to the shading effect of suspended sediment, as well as potential reservoirs for stress-tolerant species. However, little research exists on the impact of sedimentation on coral physiology, particularly at the molecular level. Here, we investigated the transcriptomic response to sediment stress in corals of the family Merulinidae from a chronically turbid reef (one genet each of Goniastrea pectinata and Mycedium elephantotus from Singapore) and a clear-water reef (multiple genets of G. pectinata from the Gulf of Aqaba/Eilat). In two ex-situ experiments, we exposed corals to either natural sediment or artificial sediment enriched with organic matter and used whole-transcriptome sequencing (RNA sequencing) to quantify gene expression. Analysis revealed a shared basis for the coral transcriptomic response to sediment stress, which involves the expression of genes broadly related to energy metabolism and immune response. In particular, sediment exposure induced upregulation of anaerobic glycolysis and glyoxylate bypass enzymes, as well as genes involved in hydrogen sulphide metabolism and in pathogen pattern recognition. Our results point towards hypoxia as a probable driver of this transcriptomic response, providing a molecular basis to previous work that identified hypoxia as a primary cause of tissue necrosis in sediment-stressed corals. Potential metabolic and immunity trade-offs of corals living under chronic sedimentation should be considered in future studies on the ecology and conservation of turbid reefs.

KW - Indo-Pacific

KW - marginal reefs

KW - Scleractinia

KW - transcriptomics

KW - turbid reefs

KW - urbanization

U2 - 10.1111/mec.16263

DO - 10.1111/mec.16263

M3 - Journal article

C2 - 34738686

AN - SCOPUS:85119593613

VL - 31

SP - 884

EP - 901

JO - Molecular Ecology

JF - Molecular Ecology

SN - 0962-1083

IS - 3

ER -

ID: 286489909