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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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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. |
format | Online Article Text |
id | pubmed-3462115 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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