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Breakdown of microbial networks links nutrient stress and reef coral disease

Breakdown of microbial networks links nutrient stress and reef coral disease
Breakdown of microbial networks links nutrient stress and reef coral disease
Coral diseases are increasing in prevalence, accelerating the global decline of tropical reefs, which threatens over 25% of marine biodiversity and vital ecosystem services for human societies. While outbreaks are frequently linked to environmental change, including heat stress, sedimentation, and reduced water quality, the mechanisms by which such factors promote disease remain poorly understood. Here we show that nutrient stress, caused by skewed seawater nitrogen-to-phosphorus (N:P) stoichiometry, promotes the onset of Black Band Disease (BBD), a common and easily recognisable syndrome that affects corals around the globe. Using Turbinaria reniformis as a model system, controlled laboratory experiments demonstrate that skewed N:P ratios disrupt the functional integrity of coral-associated microbial networks while favouring opportunists that exploit dysfunctional host–symbiont interactions. Disease lesion-associated microbial mats are dominated by cyanobacteria and include sulphur-metabolising bacteria, hallmarks of natural BBD communities. Strikingly, similar cyanobacterial taxa are also detected in the visually healthy coral tissue ahead of the expanding lesions, suggesting an opportunistic recruitment of disease-associated members from the resident microbiome. Global analyses of BBD outbreaks reveal that over 88% occurred in regions with skewed N:P ratios, compared with only 16% that were linked to prior heat stress. Together, our findings identify nutrient-driven microbiome destabilisation as a key pathway to coral disease, reinforcing nutrient management as a major lever for reef conservation and restoration practice.
2041-1723
Gracie, Raphaela
a8637a3a-0e80-4fec-841b-e2a0df1e2bfd
Wiedenmann, Joerg
ad445af2-680f-4927-90b3-589ac9d538f7
Lam, Phyllis
996aef80-a15d-4827-aed8-1b97b378f6ad
Sweet, Michael
6cf8b4e9-cfab-49fb-9acf-fa4b1ce1bea9
D'Angelo, Cecilia
0d35b03b-684d-43aa-a57a-87212ab07ee1
Gracie, Raphaela
a8637a3a-0e80-4fec-841b-e2a0df1e2bfd
Wiedenmann, Joerg
ad445af2-680f-4927-90b3-589ac9d538f7
Lam, Phyllis
996aef80-a15d-4827-aed8-1b97b378f6ad
Sweet, Michael
6cf8b4e9-cfab-49fb-9acf-fa4b1ce1bea9
D'Angelo, Cecilia
0d35b03b-684d-43aa-a57a-87212ab07ee1

Gracie, Raphaela, Wiedenmann, Joerg, Lam, Phyllis, Sweet, Michael and D'Angelo, Cecilia (2026) Breakdown of microbial networks links nutrient stress and reef coral disease. Nature Communications, 17 (3821), [3821]. (doi:10.1038/s41467-026-72175-4).

Record type: Article

Abstract

Coral diseases are increasing in prevalence, accelerating the global decline of tropical reefs, which threatens over 25% of marine biodiversity and vital ecosystem services for human societies. While outbreaks are frequently linked to environmental change, including heat stress, sedimentation, and reduced water quality, the mechanisms by which such factors promote disease remain poorly understood. Here we show that nutrient stress, caused by skewed seawater nitrogen-to-phosphorus (N:P) stoichiometry, promotes the onset of Black Band Disease (BBD), a common and easily recognisable syndrome that affects corals around the globe. Using Turbinaria reniformis as a model system, controlled laboratory experiments demonstrate that skewed N:P ratios disrupt the functional integrity of coral-associated microbial networks while favouring opportunists that exploit dysfunctional host–symbiont interactions. Disease lesion-associated microbial mats are dominated by cyanobacteria and include sulphur-metabolising bacteria, hallmarks of natural BBD communities. Strikingly, similar cyanobacterial taxa are also detected in the visually healthy coral tissue ahead of the expanding lesions, suggesting an opportunistic recruitment of disease-associated members from the resident microbiome. Global analyses of BBD outbreaks reveal that over 88% occurred in regions with skewed N:P ratios, compared with only 16% that were linked to prior heat stress. Together, our findings identify nutrient-driven microbiome destabilisation as a key pathway to coral disease, reinforcing nutrient management as a major lever for reef conservation and restoration practice.

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More information

Accepted/In Press date: 9 April 2026
Published date: 5 May 2026
Additional Information: Publisher Copyright: © The Author(s) 2026.

Identifiers

Local EPrints ID: 512466
URI: https://eprints.soton.ac.uk/id/eprint/512466
ISSN: 2041-1723
PURE UUID: 8abb6190-d18a-48c7-8d16-399ff9df7f00
ORCID for Raphaela Gracie: ORCID iD orcid.org/0000-0002-4228-6970
ORCID for Joerg Wiedenmann: ORCID iD orcid.org/0000-0003-2128-2943
ORCID for Phyllis Lam: ORCID iD orcid.org/0000-0003-2067-171X
ORCID for Cecilia D'Angelo: ORCID iD orcid.org/0000-0002-2339-6365

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Date deposited: 30 Jun 2026 17:07
Last modified: 13 Sep 2026 15:49

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Contributors

Author: Raphaela Gracie ORCID iD
Author: Phyllis Lam ORCID iD
Author: Michael Sweet

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