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Brucella ceti and Brucella pinnipedialis genome characterization unveil genetic features that highlight their zoonotic potential

The Gram‐negative bacteria Brucella ceti and Brucella pinnipedialis circulate in marine environments primarily infecting marine mammals, where they cause an often‐fatal disease named brucellosis. The increase of brucellosis among several species of cetaceans and pinnipeds, together with the report o...

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Autores principales: Orsini, Massimiliano, Ianni, Andrea, Zinzula, Luca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9597259/
https://www.ncbi.nlm.nih.gov/pubmed/36314752
http://dx.doi.org/10.1002/mbo3.1329
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author Orsini, Massimiliano
Ianni, Andrea
Zinzula, Luca
author_facet Orsini, Massimiliano
Ianni, Andrea
Zinzula, Luca
author_sort Orsini, Massimiliano
collection PubMed
description The Gram‐negative bacteria Brucella ceti and Brucella pinnipedialis circulate in marine environments primarily infecting marine mammals, where they cause an often‐fatal disease named brucellosis. The increase of brucellosis among several species of cetaceans and pinnipeds, together with the report of sporadic human infections, raises concerns about the zoonotic potential of these pathogens on a large scale and may pose a threat to coastal communities worldwide. Therefore, the characterization of the B. ceti and B. pinnipedialis genetic features is a priority to better understand the pathological factors that may impact global health. Moreover, an in‐depth functional analysis of the B. ceti and B. pinnipedialis genome in the context of virulence and pathogenesis was not undertaken so far. Within this picture, here we present the comparative whole‐genome characterization of all B. ceti and B. pinnipedialis genomes available in public resources, uncovering a collection of genetic tools possessed by these aquatic bacterial species compared to their zoonotic terrestrial relatives. We show that B. ceti and B. pinnipedialis genomes display a wide host‐range infection capability and a polyphyletic phylogeny within the genus, showing a genomic structure that fits the canonical definition of closeness. Functional genome annotation led to identifying genes related to several pathways involved in mechanisms of infection, others conferring pan‐susceptibility to antimicrobials and a set of virulence genes that highlight the similarity of B. ceti and B. pinnipedialis genotypes to those of Brucella spp. displaying human‐infecting phenotypes.
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spelling pubmed-95972592022-10-27 Brucella ceti and Brucella pinnipedialis genome characterization unveil genetic features that highlight their zoonotic potential Orsini, Massimiliano Ianni, Andrea Zinzula, Luca Microbiologyopen Original Articles The Gram‐negative bacteria Brucella ceti and Brucella pinnipedialis circulate in marine environments primarily infecting marine mammals, where they cause an often‐fatal disease named brucellosis. The increase of brucellosis among several species of cetaceans and pinnipeds, together with the report of sporadic human infections, raises concerns about the zoonotic potential of these pathogens on a large scale and may pose a threat to coastal communities worldwide. Therefore, the characterization of the B. ceti and B. pinnipedialis genetic features is a priority to better understand the pathological factors that may impact global health. Moreover, an in‐depth functional analysis of the B. ceti and B. pinnipedialis genome in the context of virulence and pathogenesis was not undertaken so far. Within this picture, here we present the comparative whole‐genome characterization of all B. ceti and B. pinnipedialis genomes available in public resources, uncovering a collection of genetic tools possessed by these aquatic bacterial species compared to their zoonotic terrestrial relatives. We show that B. ceti and B. pinnipedialis genomes display a wide host‐range infection capability and a polyphyletic phylogeny within the genus, showing a genomic structure that fits the canonical definition of closeness. Functional genome annotation led to identifying genes related to several pathways involved in mechanisms of infection, others conferring pan‐susceptibility to antimicrobials and a set of virulence genes that highlight the similarity of B. ceti and B. pinnipedialis genotypes to those of Brucella spp. displaying human‐infecting phenotypes. John Wiley and Sons Inc. 2022-10-26 /pmc/articles/PMC9597259/ /pubmed/36314752 http://dx.doi.org/10.1002/mbo3.1329 Text en © 2022 The Authors. MicrobiologyOpen published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Orsini, Massimiliano
Ianni, Andrea
Zinzula, Luca
Brucella ceti and Brucella pinnipedialis genome characterization unveil genetic features that highlight their zoonotic potential
title Brucella ceti and Brucella pinnipedialis genome characterization unveil genetic features that highlight their zoonotic potential
title_full Brucella ceti and Brucella pinnipedialis genome characterization unveil genetic features that highlight their zoonotic potential
title_fullStr Brucella ceti and Brucella pinnipedialis genome characterization unveil genetic features that highlight their zoonotic potential
title_full_unstemmed Brucella ceti and Brucella pinnipedialis genome characterization unveil genetic features that highlight their zoonotic potential
title_short Brucella ceti and Brucella pinnipedialis genome characterization unveil genetic features that highlight their zoonotic potential
title_sort brucella ceti and brucella pinnipedialis genome characterization unveil genetic features that highlight their zoonotic potential
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9597259/
https://www.ncbi.nlm.nih.gov/pubmed/36314752
http://dx.doi.org/10.1002/mbo3.1329
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