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Cellular traits regulate fluorescence-based light-response phenotypes of coral photosymbionts living in-hospite

Diversity across algal family Symbiodiniaceae contributes to the environmental resilience of certain coral species. Chlorophyll-a fluorescence measurements are frequently used to determine symbiont health and resilience, but more work is needed to refine these tools and establish how they relate to...

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Autores principales: McQuagge, Audrey, Pahl, K. Blue, Wong, Sophie, Melman, Todd, Linn, Laura, Lowry, Sean, Hoadley, Kenneth D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10598705/
https://www.ncbi.nlm.nih.gov/pubmed/37885802
http://dx.doi.org/10.3389/fphys.2023.1244060
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author McQuagge, Audrey
Pahl, K. Blue
Wong, Sophie
Melman, Todd
Linn, Laura
Lowry, Sean
Hoadley, Kenneth D.
author_facet McQuagge, Audrey
Pahl, K. Blue
Wong, Sophie
Melman, Todd
Linn, Laura
Lowry, Sean
Hoadley, Kenneth D.
author_sort McQuagge, Audrey
collection PubMed
description Diversity across algal family Symbiodiniaceae contributes to the environmental resilience of certain coral species. Chlorophyll-a fluorescence measurements are frequently used to determine symbiont health and resilience, but more work is needed to refine these tools and establish how they relate to underlying cellular traits. We examined trait diversity in symbionts from the generas Cladocopium and Durusdinium, collected from 12 aquacultured coral species. Photophysiological metrics (Φ(PSII), σ(PSII), ρ, τ(1), τ(2), antenna bed quenching, non-photochemical quenching, and qP) were assessed using a prototype multi-spectral fluorometer over a variable light protocol which yielded a total of 1,360 individual metrics. Photophysiological metrics were then used to establish four unique light-response phenotypic variants. Corals harboring C15 were predominantly found within a single light-response phenotype which clustered separately from all other coral fragments. The majority of Durusdinium dominated colonies also formed a separate light-response phenotype which it shared with a few C1 dominated corals. C15 and D1 symbionts appear to differ in which mechanisms they use to dissipate excess light energy. Spectrally dependent variability is also observed across light-response phenotypes that may relate to differences in photopigment utilization. Symbiont cell biochemical and structural traits (atomic C:N:P, cell size, chlorophyll-a, neutral lipid content) was also assessed within each sample and differ across light-response phenotypes, linking photophysiological metrics with underlying primary cellular traits. Strong correlations between first- and second-order traits, such as Quantum Yield and cellular N:P content, or light dissipation pathways (qP and NPQ) and C:P underline differences across symbiont types and may also provide a means for using fluorescence-based metrics as biomarkers for certain primary-cellular traits.
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spelling pubmed-105987052023-10-26 Cellular traits regulate fluorescence-based light-response phenotypes of coral photosymbionts living in-hospite McQuagge, Audrey Pahl, K. Blue Wong, Sophie Melman, Todd Linn, Laura Lowry, Sean Hoadley, Kenneth D. Front Physiol Physiology Diversity across algal family Symbiodiniaceae contributes to the environmental resilience of certain coral species. Chlorophyll-a fluorescence measurements are frequently used to determine symbiont health and resilience, but more work is needed to refine these tools and establish how they relate to underlying cellular traits. We examined trait diversity in symbionts from the generas Cladocopium and Durusdinium, collected from 12 aquacultured coral species. Photophysiological metrics (Φ(PSII), σ(PSII), ρ, τ(1), τ(2), antenna bed quenching, non-photochemical quenching, and qP) were assessed using a prototype multi-spectral fluorometer over a variable light protocol which yielded a total of 1,360 individual metrics. Photophysiological metrics were then used to establish four unique light-response phenotypic variants. Corals harboring C15 were predominantly found within a single light-response phenotype which clustered separately from all other coral fragments. The majority of Durusdinium dominated colonies also formed a separate light-response phenotype which it shared with a few C1 dominated corals. C15 and D1 symbionts appear to differ in which mechanisms they use to dissipate excess light energy. Spectrally dependent variability is also observed across light-response phenotypes that may relate to differences in photopigment utilization. Symbiont cell biochemical and structural traits (atomic C:N:P, cell size, chlorophyll-a, neutral lipid content) was also assessed within each sample and differ across light-response phenotypes, linking photophysiological metrics with underlying primary cellular traits. Strong correlations between first- and second-order traits, such as Quantum Yield and cellular N:P content, or light dissipation pathways (qP and NPQ) and C:P underline differences across symbiont types and may also provide a means for using fluorescence-based metrics as biomarkers for certain primary-cellular traits. Frontiers Media S.A. 2023-10-11 /pmc/articles/PMC10598705/ /pubmed/37885802 http://dx.doi.org/10.3389/fphys.2023.1244060 Text en Copyright © 2023 McQuagge, Pahl, Wong, Melman, Linn, Lowry and Hoadley. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
McQuagge, Audrey
Pahl, K. Blue
Wong, Sophie
Melman, Todd
Linn, Laura
Lowry, Sean
Hoadley, Kenneth D.
Cellular traits regulate fluorescence-based light-response phenotypes of coral photosymbionts living in-hospite
title Cellular traits regulate fluorescence-based light-response phenotypes of coral photosymbionts living in-hospite
title_full Cellular traits regulate fluorescence-based light-response phenotypes of coral photosymbionts living in-hospite
title_fullStr Cellular traits regulate fluorescence-based light-response phenotypes of coral photosymbionts living in-hospite
title_full_unstemmed Cellular traits regulate fluorescence-based light-response phenotypes of coral photosymbionts living in-hospite
title_short Cellular traits regulate fluorescence-based light-response phenotypes of coral photosymbionts living in-hospite
title_sort cellular traits regulate fluorescence-based light-response phenotypes of coral photosymbionts living in-hospite
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10598705/
https://www.ncbi.nlm.nih.gov/pubmed/37885802
http://dx.doi.org/10.3389/fphys.2023.1244060
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