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Protective role of the vulture facial skin and gut microbiomes aid adaptation to scavenging

BACKGROUND: Vultures have adapted the remarkable ability to feed on carcasses that may contain microorganisms that would be pathogenic to most other animals. The holobiont concept suggests that the genetic basis of such adaptation may not only lie within their genomes, but additionally in their asso...

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Autores principales: Zepeda Mendoza, Marie Lisandra, Roggenbuck, Michael, Manzano Vargas, Karla, Hansen, Lars Hestbjerg, Brunak, Søren, Gilbert, M. Thomas P., Sicheritz-Pontén, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6182802/
https://www.ncbi.nlm.nih.gov/pubmed/30309375
http://dx.doi.org/10.1186/s13028-018-0415-3
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author Zepeda Mendoza, Marie Lisandra
Roggenbuck, Michael
Manzano Vargas, Karla
Hansen, Lars Hestbjerg
Brunak, Søren
Gilbert, M. Thomas P.
Sicheritz-Pontén, Thomas
author_facet Zepeda Mendoza, Marie Lisandra
Roggenbuck, Michael
Manzano Vargas, Karla
Hansen, Lars Hestbjerg
Brunak, Søren
Gilbert, M. Thomas P.
Sicheritz-Pontén, Thomas
author_sort Zepeda Mendoza, Marie Lisandra
collection PubMed
description BACKGROUND: Vultures have adapted the remarkable ability to feed on carcasses that may contain microorganisms that would be pathogenic to most other animals. The holobiont concept suggests that the genetic basis of such adaptation may not only lie within their genomes, but additionally in their associated microbes. To explore this, we generated shotgun DNA sequencing datasets of the facial skin and large intestine microbiomes of the black vulture (Coragyps atratus) and the turkey vulture (Cathartes aura). We characterized the functional potential and taxonomic diversity of their microbiomes, the potential pathogenic challenges confronted by vultures, and the microbial taxa and genes that could play a protective role on the facial skin and in the gut. RESULTS: We found microbial taxa and genes involved in diseases, such as dermatitis and pneumonia (more abundant on the facial skin), and gas gangrene and food poisoning (more abundant in the gut). Interestingly, we found taxa and functions with potential for playing beneficial roles, such as antilisterial bacteria in the gut, and genes for the production of antiparasitics and insecticides on the facial skin. Based on the identified phages, we suggest that phages aid in the control and possibly elimination, as in phage therapy, of microbes reported as pathogenic to a variety of species. Interestingly, we identified Adineta vaga in the gut, an invertebrate that feeds on dead bacteria and protozoans, suggesting a defensive predatory mechanism. Finally, we suggest a colonization resistance role through biofilm formation played by Fusobacteria and Clostridia in the gut. CONCLUSIONS: Our results highlight the importance of complementing genomic analyses with metagenomics in order to obtain a clearer understanding of the host-microbial alliance and show the importance of microbiome-mediated health protection for adaptation to extreme diets, such as scavenging. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13028-018-0415-3) contains supplementary material, which is available to authorized users.
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spelling pubmed-61828022018-10-18 Protective role of the vulture facial skin and gut microbiomes aid adaptation to scavenging Zepeda Mendoza, Marie Lisandra Roggenbuck, Michael Manzano Vargas, Karla Hansen, Lars Hestbjerg Brunak, Søren Gilbert, M. Thomas P. Sicheritz-Pontén, Thomas Acta Vet Scand Research BACKGROUND: Vultures have adapted the remarkable ability to feed on carcasses that may contain microorganisms that would be pathogenic to most other animals. The holobiont concept suggests that the genetic basis of such adaptation may not only lie within their genomes, but additionally in their associated microbes. To explore this, we generated shotgun DNA sequencing datasets of the facial skin and large intestine microbiomes of the black vulture (Coragyps atratus) and the turkey vulture (Cathartes aura). We characterized the functional potential and taxonomic diversity of their microbiomes, the potential pathogenic challenges confronted by vultures, and the microbial taxa and genes that could play a protective role on the facial skin and in the gut. RESULTS: We found microbial taxa and genes involved in diseases, such as dermatitis and pneumonia (more abundant on the facial skin), and gas gangrene and food poisoning (more abundant in the gut). Interestingly, we found taxa and functions with potential for playing beneficial roles, such as antilisterial bacteria in the gut, and genes for the production of antiparasitics and insecticides on the facial skin. Based on the identified phages, we suggest that phages aid in the control and possibly elimination, as in phage therapy, of microbes reported as pathogenic to a variety of species. Interestingly, we identified Adineta vaga in the gut, an invertebrate that feeds on dead bacteria and protozoans, suggesting a defensive predatory mechanism. Finally, we suggest a colonization resistance role through biofilm formation played by Fusobacteria and Clostridia in the gut. CONCLUSIONS: Our results highlight the importance of complementing genomic analyses with metagenomics in order to obtain a clearer understanding of the host-microbial alliance and show the importance of microbiome-mediated health protection for adaptation to extreme diets, such as scavenging. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13028-018-0415-3) contains supplementary material, which is available to authorized users. BioMed Central 2018-10-11 /pmc/articles/PMC6182802/ /pubmed/30309375 http://dx.doi.org/10.1186/s13028-018-0415-3 Text en © The Author(s) 2018 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
Zepeda Mendoza, Marie Lisandra
Roggenbuck, Michael
Manzano Vargas, Karla
Hansen, Lars Hestbjerg
Brunak, Søren
Gilbert, M. Thomas P.
Sicheritz-Pontén, Thomas
Protective role of the vulture facial skin and gut microbiomes aid adaptation to scavenging
title Protective role of the vulture facial skin and gut microbiomes aid adaptation to scavenging
title_full Protective role of the vulture facial skin and gut microbiomes aid adaptation to scavenging
title_fullStr Protective role of the vulture facial skin and gut microbiomes aid adaptation to scavenging
title_full_unstemmed Protective role of the vulture facial skin and gut microbiomes aid adaptation to scavenging
title_short Protective role of the vulture facial skin and gut microbiomes aid adaptation to scavenging
title_sort protective role of the vulture facial skin and gut microbiomes aid adaptation to scavenging
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6182802/
https://www.ncbi.nlm.nih.gov/pubmed/30309375
http://dx.doi.org/10.1186/s13028-018-0415-3
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