ArticleScientific reports2017
Intra-colony disease progression induces fragmentation of coral fluorescent pigments.
Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 3 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
3 citing papers in PubMed, 12 citations in OpenAlex.
- Spatial extent of dysbiosis in the branching coral Pocillopora damicornis during an acute disease outbreak.Scientific reports · 2023Article
- Effect of self-assembly on fluorescence in magnetic multiphase flows and its application on the novel detection for COVID-19.Physics of fluids (Woodbury, N.Y. : 1994) · 2021Article
- Applying model approaches in non-model systems: A review and case study on coral cell culture.PloS one · 2021Review
Corrections and comments
- Erratum issued
- Erratum issued
Authors and funding
4 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
As disease spreads through living coral, it can induce changes in the distribution of coral's naturally fluorescent pigments, making fluorescence a potentially powerful non-invasive intrinsic marker of coral disease. Here, we show the usefulness of live-imaging laser scanning confocal microscopy to investigate coral health state. We demonstrate that the Hawaiian coral Montipora capitata consistently emits cyan and red fluorescence across a depth gradient in reef habitats, but the micro-scale spatial distribution of those pigments differ between healthy coral and coral affected by a tissue loss disease. Naturally diseased and laboratory infected coral systematically exhibited fragmented fluorescent pigments adjacent to the disease front as indicated by several measures of landscape structure (e.g., number of patches) relative to healthy coral. Histology results supported these findings. Pigment fragmentation indicates a disruption in coral tissue that likely impedes translocation of energy within a colony. The area of fragmented fluorescent pigments in diseased coral extended 3.03 mm ± 1.80 mm adjacent to the disease front, indicating pathogenesis was highly localized rather than systemic. Our study demonstrates that coral fluorescence can be used as a proxy for coral health state, and, such patterns may help refine hypotheses about modes of pathogenesis.
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Registered trials
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