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Gill-associated bacteria are homogeneously selected in amphibious mangrove crabs to sustain host intertidal adaptation

BACKGROUND: The transition from water to air is a key event in the evolution of many marine organisms to access new food sources, escape water hypoxia, and exploit the higher and temperature-independent oxygen concentration of air. Despite the importance of microorganisms in host adaptation, their c...

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Autores principales: Fusi, Marco, Ngugi, David K., Marasco, Ramona, Booth, Jenny Marie, Cardinale, Massimiliano, Sacchi, Luciano, Clementi, Emanuela, Yang, Xinyuan, Garuglieri, Elisa, Fodelianakis, Stilianos, Michoud, Grégoire, Daffonchio, Daniele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10463870/
https://www.ncbi.nlm.nih.gov/pubmed/37612775
http://dx.doi.org/10.1186/s40168-023-01629-4
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author Fusi, Marco
Ngugi, David K.
Marasco, Ramona
Booth, Jenny Marie
Cardinale, Massimiliano
Sacchi, Luciano
Clementi, Emanuela
Yang, Xinyuan
Garuglieri, Elisa
Fodelianakis, Stilianos
Michoud, Grégoire
Daffonchio, Daniele
author_facet Fusi, Marco
Ngugi, David K.
Marasco, Ramona
Booth, Jenny Marie
Cardinale, Massimiliano
Sacchi, Luciano
Clementi, Emanuela
Yang, Xinyuan
Garuglieri, Elisa
Fodelianakis, Stilianos
Michoud, Grégoire
Daffonchio, Daniele
author_sort Fusi, Marco
collection PubMed
description BACKGROUND: The transition from water to air is a key event in the evolution of many marine organisms to access new food sources, escape water hypoxia, and exploit the higher and temperature-independent oxygen concentration of air. Despite the importance of microorganisms in host adaptation, their contribution to overcoming the challenges posed by the lifestyle changes from water to land is not well understood. To address this, we examined how microbial association with a key multifunctional organ, the gill, is involved in the intertidal adaptation of fiddler crabs, a dual-breathing organism. RESULTS: Electron microscopy revealed a rod-shaped bacterial layer tightly connected to the gill lamellae of the five crab species sampled across a latitudinal gradient from the central Red Sea to the southern Indian Ocean. The gill bacterial community diversity assessed with 16S rRNA gene amplicon sequencing was consistently low across crab species, and the same actinobacterial group, namely Ilumatobacter, was dominant regardless of the geographic location of the host. Using metagenomics and metatranscriptomics, we detected that these members of actinobacteria are potentially able to convert ammonia to amino acids and may help eliminate toxic sulphur compounds and carbon monoxide to which crabs are constantly exposed. CONCLUSIONS: These results indicate that bacteria selected on gills can play a role in the adaptation of animals in dynamic intertidal ecosystems. Hence, this relationship is likely to be important in the ecological and evolutionary processes of the transition from water to air and deserves further attention, including the ontogenetic onset of this association. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-023-01629-4.
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spelling pubmed-104638702023-08-30 Gill-associated bacteria are homogeneously selected in amphibious mangrove crabs to sustain host intertidal adaptation Fusi, Marco Ngugi, David K. Marasco, Ramona Booth, Jenny Marie Cardinale, Massimiliano Sacchi, Luciano Clementi, Emanuela Yang, Xinyuan Garuglieri, Elisa Fodelianakis, Stilianos Michoud, Grégoire Daffonchio, Daniele Microbiome Research BACKGROUND: The transition from water to air is a key event in the evolution of many marine organisms to access new food sources, escape water hypoxia, and exploit the higher and temperature-independent oxygen concentration of air. Despite the importance of microorganisms in host adaptation, their contribution to overcoming the challenges posed by the lifestyle changes from water to land is not well understood. To address this, we examined how microbial association with a key multifunctional organ, the gill, is involved in the intertidal adaptation of fiddler crabs, a dual-breathing organism. RESULTS: Electron microscopy revealed a rod-shaped bacterial layer tightly connected to the gill lamellae of the five crab species sampled across a latitudinal gradient from the central Red Sea to the southern Indian Ocean. The gill bacterial community diversity assessed with 16S rRNA gene amplicon sequencing was consistently low across crab species, and the same actinobacterial group, namely Ilumatobacter, was dominant regardless of the geographic location of the host. Using metagenomics and metatranscriptomics, we detected that these members of actinobacteria are potentially able to convert ammonia to amino acids and may help eliminate toxic sulphur compounds and carbon monoxide to which crabs are constantly exposed. CONCLUSIONS: These results indicate that bacteria selected on gills can play a role in the adaptation of animals in dynamic intertidal ecosystems. Hence, this relationship is likely to be important in the ecological and evolutionary processes of the transition from water to air and deserves further attention, including the ontogenetic onset of this association. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-023-01629-4. BioMed Central 2023-08-24 /pmc/articles/PMC10463870/ /pubmed/37612775 http://dx.doi.org/10.1186/s40168-023-01629-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Fusi, Marco
Ngugi, David K.
Marasco, Ramona
Booth, Jenny Marie
Cardinale, Massimiliano
Sacchi, Luciano
Clementi, Emanuela
Yang, Xinyuan
Garuglieri, Elisa
Fodelianakis, Stilianos
Michoud, Grégoire
Daffonchio, Daniele
Gill-associated bacteria are homogeneously selected in amphibious mangrove crabs to sustain host intertidal adaptation
title Gill-associated bacteria are homogeneously selected in amphibious mangrove crabs to sustain host intertidal adaptation
title_full Gill-associated bacteria are homogeneously selected in amphibious mangrove crabs to sustain host intertidal adaptation
title_fullStr Gill-associated bacteria are homogeneously selected in amphibious mangrove crabs to sustain host intertidal adaptation
title_full_unstemmed Gill-associated bacteria are homogeneously selected in amphibious mangrove crabs to sustain host intertidal adaptation
title_short Gill-associated bacteria are homogeneously selected in amphibious mangrove crabs to sustain host intertidal adaptation
title_sort gill-associated bacteria are homogeneously selected in amphibious mangrove crabs to sustain host intertidal adaptation
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10463870/
https://www.ncbi.nlm.nih.gov/pubmed/37612775
http://dx.doi.org/10.1186/s40168-023-01629-4
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