Cargando…
Wild eel microbiome reveals that skin mucus of fish could be a natural niche for aquatic mucosal pathogen evolution
BACKGROUND: Fish skin mucosal surfaces (SMS) are quite similar in composition and function to some mammalian MS and, in consequence, could constitute an adequate niche for the evolution of mucosal aquatic pathogens in natural environments. We aimed to test this hypothesis by searching for metagenomi...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5740887/ https://www.ncbi.nlm.nih.gov/pubmed/29268781 http://dx.doi.org/10.1186/s40168-017-0376-1 |
_version_ | 1783288100275879936 |
---|---|
author | Carda-Diéguez, Miguel Ghai, Rohit Rodríguez-Valera, Francisco Amaro, Carmen |
author_facet | Carda-Diéguez, Miguel Ghai, Rohit Rodríguez-Valera, Francisco Amaro, Carmen |
author_sort | Carda-Diéguez, Miguel |
collection | PubMed |
description | BACKGROUND: Fish skin mucosal surfaces (SMS) are quite similar in composition and function to some mammalian MS and, in consequence, could constitute an adequate niche for the evolution of mucosal aquatic pathogens in natural environments. We aimed to test this hypothesis by searching for metagenomic and genomic evidences in the SMS-microbiome of a model fish species (Anguilla Anguilla or eel), from different ecosystems (four natural environments of different water salinity and one eel farm) as well as the water microbiome (W-microbiome) surrounding the host. RESULTS: Remarkably, potentially pathogenic Vibrio monopolized wild eel SMS-microbiome from natural ecosystems, Vibrio anguillarum/Vibrio vulnificus and Vibrio cholerae/Vibrio metoecus being the most abundant ones in SMS from estuary and lake, respectively. Functions encoded in the SMS-microbiome differed significantly from those in the W-microbiome and allowed us to predict that successful mucus colonizers should have specific genes for (i) attachment (mainly by forming biofilms), (ii) bacterial competence and communication, and (iii) resistance to mucosal innate immunity, predators (amoeba), and heavy metals/drugs. In addition, we found several mobile genetic elements (mainly integrative conjugative elements) as well as a series of evidences suggesting that bacteria exchange DNA in SMS. Further, we isolated and sequenced a V. metoecus strain from SMS. This isolate shares pathogenicity islands with V. cholerae O1 from intestinal infections that are absent in the rest of sequenced V. metoecus strains, all of them from water and extra-intestinal infections. CONCLUSIONS: We have obtained metagenomic and genomic evidence in favor of the hypothesis on the role of fish mucosal surfaces as a specialized habitat selecting microbes capable of colonizing and persisting on other comparable mucosal surfaces, e.g., the human intestine. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40168-017-0376-1) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5740887 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-57408872018-01-03 Wild eel microbiome reveals that skin mucus of fish could be a natural niche for aquatic mucosal pathogen evolution Carda-Diéguez, Miguel Ghai, Rohit Rodríguez-Valera, Francisco Amaro, Carmen Microbiome Research BACKGROUND: Fish skin mucosal surfaces (SMS) are quite similar in composition and function to some mammalian MS and, in consequence, could constitute an adequate niche for the evolution of mucosal aquatic pathogens in natural environments. We aimed to test this hypothesis by searching for metagenomic and genomic evidences in the SMS-microbiome of a model fish species (Anguilla Anguilla or eel), from different ecosystems (four natural environments of different water salinity and one eel farm) as well as the water microbiome (W-microbiome) surrounding the host. RESULTS: Remarkably, potentially pathogenic Vibrio monopolized wild eel SMS-microbiome from natural ecosystems, Vibrio anguillarum/Vibrio vulnificus and Vibrio cholerae/Vibrio metoecus being the most abundant ones in SMS from estuary and lake, respectively. Functions encoded in the SMS-microbiome differed significantly from those in the W-microbiome and allowed us to predict that successful mucus colonizers should have specific genes for (i) attachment (mainly by forming biofilms), (ii) bacterial competence and communication, and (iii) resistance to mucosal innate immunity, predators (amoeba), and heavy metals/drugs. In addition, we found several mobile genetic elements (mainly integrative conjugative elements) as well as a series of evidences suggesting that bacteria exchange DNA in SMS. Further, we isolated and sequenced a V. metoecus strain from SMS. This isolate shares pathogenicity islands with V. cholerae O1 from intestinal infections that are absent in the rest of sequenced V. metoecus strains, all of them from water and extra-intestinal infections. CONCLUSIONS: We have obtained metagenomic and genomic evidence in favor of the hypothesis on the role of fish mucosal surfaces as a specialized habitat selecting microbes capable of colonizing and persisting on other comparable mucosal surfaces, e.g., the human intestine. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40168-017-0376-1) contains supplementary material, which is available to authorized users. BioMed Central 2017-12-21 /pmc/articles/PMC5740887/ /pubmed/29268781 http://dx.doi.org/10.1186/s40168-017-0376-1 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Carda-Diéguez, Miguel Ghai, Rohit Rodríguez-Valera, Francisco Amaro, Carmen Wild eel microbiome reveals that skin mucus of fish could be a natural niche for aquatic mucosal pathogen evolution |
title | Wild eel microbiome reveals that skin mucus of fish could be a natural niche for aquatic mucosal pathogen evolution |
title_full | Wild eel microbiome reveals that skin mucus of fish could be a natural niche for aquatic mucosal pathogen evolution |
title_fullStr | Wild eel microbiome reveals that skin mucus of fish could be a natural niche for aquatic mucosal pathogen evolution |
title_full_unstemmed | Wild eel microbiome reveals that skin mucus of fish could be a natural niche for aquatic mucosal pathogen evolution |
title_short | Wild eel microbiome reveals that skin mucus of fish could be a natural niche for aquatic mucosal pathogen evolution |
title_sort | wild eel microbiome reveals that skin mucus of fish could be a natural niche for aquatic mucosal pathogen evolution |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5740887/ https://www.ncbi.nlm.nih.gov/pubmed/29268781 http://dx.doi.org/10.1186/s40168-017-0376-1 |
work_keys_str_mv | AT cardadieguezmiguel wildeelmicrobiomerevealsthatskinmucusoffishcouldbeanaturalnicheforaquaticmucosalpathogenevolution AT ghairohit wildeelmicrobiomerevealsthatskinmucusoffishcouldbeanaturalnicheforaquaticmucosalpathogenevolution AT rodriguezvalerafrancisco wildeelmicrobiomerevealsthatskinmucusoffishcouldbeanaturalnicheforaquaticmucosalpathogenevolution AT amarocarmen wildeelmicrobiomerevealsthatskinmucusoffishcouldbeanaturalnicheforaquaticmucosalpathogenevolution |