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Phenotypic and Genomic Analysis of Hypervirulent Human-associated Bordetella bronchiseptica

BACKGROUND: B. bronchiseptica infections are usually associated with wild or domesticated animals, but infrequently with humans. A recent phylogenetic analysis distinguished two distinct B. bronchiseptica subpopulations, designated complexes I and IV. Complex IV isolates appear to have a bias for in...

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Autores principales: Ahuja, Umesh, Liu, Minghsun, Tomida, Shuta, Park, Jihye, Souda, Puneet, Whitelegge, Julian, Li, Huiying, Harvill, Eric T, Parkhill, Julian, Miller, Jeff F
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3462115/
https://www.ncbi.nlm.nih.gov/pubmed/22863321
http://dx.doi.org/10.1186/1471-2180-12-167
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author Ahuja, Umesh
Liu, Minghsun
Tomida, Shuta
Park, Jihye
Souda, Puneet
Whitelegge, Julian
Li, Huiying
Harvill, Eric T
Parkhill, Julian
Miller, Jeff F
author_facet Ahuja, Umesh
Liu, Minghsun
Tomida, Shuta
Park, Jihye
Souda, Puneet
Whitelegge, Julian
Li, Huiying
Harvill, Eric T
Parkhill, Julian
Miller, Jeff F
author_sort Ahuja, Umesh
collection PubMed
description BACKGROUND: B. bronchiseptica infections are usually associated with wild or domesticated animals, but infrequently with humans. A recent phylogenetic analysis distinguished two distinct B. bronchiseptica subpopulations, designated complexes I and IV. Complex IV isolates appear to have a bias for infecting humans; however, little is known regarding their epidemiology, virulence properties, or comparative genomics. RESULTS: Here we report a characterization of the virulence of human-associated complex IV B. bronchiseptica strains. In in vitro cytotoxicity assays, complex IV strains showed increased cytotoxicity in comparison to a panel of complex I strains. Some complex IV isolates were remarkably cytotoxic, resulting in LDH release levels in A549 cells that were 10- to 20-fold greater than complex I strains. In vivo, a subset of complex IV strains was found to be hypervirulent, with an increased ability to cause lethal pulmonary infections in mice. Hypercytotoxicity in vitro and hypervirulence in vivo were both dependent on the activity of the bsc T3SS and the BteA effector. To clarify differences between lineages, representative complex IV isolates were sequenced and their genomes were compared to complex I isolates. Although our analysis showed there were no genomic sequences that can be considered unique to complex IV strains, there were several loci that were predominantly found in complex IV isolates. CONCLUSION: Our observations reveal a T3SS-dependent hypervirulence phenotype in human-associated complex IV isolates, highlighting the need for further studies on the epidemiology and evolutionary dynamics of this B. bronchiseptica lineage.
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spelling pubmed-34621152012-10-02 Phenotypic and Genomic Analysis of Hypervirulent Human-associated Bordetella bronchiseptica Ahuja, Umesh Liu, Minghsun Tomida, Shuta Park, Jihye Souda, Puneet Whitelegge, Julian Li, Huiying Harvill, Eric T Parkhill, Julian Miller, Jeff F BMC Microbiol Research Article BACKGROUND: B. bronchiseptica infections are usually associated with wild or domesticated animals, but infrequently with humans. A recent phylogenetic analysis distinguished two distinct B. bronchiseptica subpopulations, designated complexes I and IV. Complex IV isolates appear to have a bias for infecting humans; however, little is known regarding their epidemiology, virulence properties, or comparative genomics. RESULTS: Here we report a characterization of the virulence of human-associated complex IV B. bronchiseptica strains. In in vitro cytotoxicity assays, complex IV strains showed increased cytotoxicity in comparison to a panel of complex I strains. Some complex IV isolates were remarkably cytotoxic, resulting in LDH release levels in A549 cells that were 10- to 20-fold greater than complex I strains. In vivo, a subset of complex IV strains was found to be hypervirulent, with an increased ability to cause lethal pulmonary infections in mice. Hypercytotoxicity in vitro and hypervirulence in vivo were both dependent on the activity of the bsc T3SS and the BteA effector. To clarify differences between lineages, representative complex IV isolates were sequenced and their genomes were compared to complex I isolates. Although our analysis showed there were no genomic sequences that can be considered unique to complex IV strains, there were several loci that were predominantly found in complex IV isolates. CONCLUSION: Our observations reveal a T3SS-dependent hypervirulence phenotype in human-associated complex IV isolates, highlighting the need for further studies on the epidemiology and evolutionary dynamics of this B. bronchiseptica lineage. BioMed Central 2012-08-06 /pmc/articles/PMC3462115/ /pubmed/22863321 http://dx.doi.org/10.1186/1471-2180-12-167 Text en Copyright ©2012 Ahuja et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Ahuja, Umesh
Liu, Minghsun
Tomida, Shuta
Park, Jihye
Souda, Puneet
Whitelegge, Julian
Li, Huiying
Harvill, Eric T
Parkhill, Julian
Miller, Jeff F
Phenotypic and Genomic Analysis of Hypervirulent Human-associated Bordetella bronchiseptica
title Phenotypic and Genomic Analysis of Hypervirulent Human-associated Bordetella bronchiseptica
title_full Phenotypic and Genomic Analysis of Hypervirulent Human-associated Bordetella bronchiseptica
title_fullStr Phenotypic and Genomic Analysis of Hypervirulent Human-associated Bordetella bronchiseptica
title_full_unstemmed Phenotypic and Genomic Analysis of Hypervirulent Human-associated Bordetella bronchiseptica
title_short Phenotypic and Genomic Analysis of Hypervirulent Human-associated Bordetella bronchiseptica
title_sort phenotypic and genomic analysis of hypervirulent human-associated bordetella bronchiseptica
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3462115/
https://www.ncbi.nlm.nih.gov/pubmed/22863321
http://dx.doi.org/10.1186/1471-2180-12-167
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