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Molecular analysis of the emergence of pandemic Vibrio parahaemolyticus

BACKGROUND: Vibrio parahaemolyticus is abundant in the aquatic environment particularly in warmer waters and is the leading cause of seafood borne gastroenteritis worldwide. Prior to 1995, numerous V. parahaemolyticus serogroups were associated with disease, however, in that year an O3:K6 serogroup...

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Autores principales: Boyd, E Fidelma, Cohen, Ana Luisa V, Naughton, Lynn M, Ussery, David W, Binnewies, Tim T, Stine, O Colin, Parent, Michelle A
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2491623/
https://www.ncbi.nlm.nih.gov/pubmed/18590559
http://dx.doi.org/10.1186/1471-2180-8-110
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author Boyd, E Fidelma
Cohen, Ana Luisa V
Naughton, Lynn M
Ussery, David W
Binnewies, Tim T
Stine, O Colin
Parent, Michelle A
author_facet Boyd, E Fidelma
Cohen, Ana Luisa V
Naughton, Lynn M
Ussery, David W
Binnewies, Tim T
Stine, O Colin
Parent, Michelle A
author_sort Boyd, E Fidelma
collection PubMed
description BACKGROUND: Vibrio parahaemolyticus is abundant in the aquatic environment particularly in warmer waters and is the leading cause of seafood borne gastroenteritis worldwide. Prior to 1995, numerous V. parahaemolyticus serogroups were associated with disease, however, in that year an O3:K6 serogroup emerged in Southeast Asia causing large outbreaks and rapid hospitalizations. This new highly virulent strain is now globally disseminated. RESULTS: We performed a four-way BLAST analysis on the genome sequence of V. parahaemolyticus RIMD2210633, an O3:K6 isolate from Japan recovered in 1996, versus the genomes of four published Vibrio species and constructed genome BLAST atlases. We identified 24 regions, gaps in the genome atlas, of greater than 10 kb that were unique to RIMD2210633. These 24 regions included an integron, f237 phage, 2 type III secretion systems (T3SS), a type VI secretion system (T6SS) and 7 Vibrio parahaemolyticus genomic islands (VPaI-1 to VPaI-7). Comparative genomic analysis of our fifth genome, V. parahaemolyticus AQ3810, an O3:K6 isolate recovered in 1983, identified four regions unique to each V. parahaemolyticus strain. Interestingly, AQ3810 did not encode 8 of the 24 regions unique to RMID, including a T6SS, which suggests an additional virulence mechanism in RIMD2210633. The distribution of only the VPaI regions was highly variable among a collection of 42 isolates and phylogenetic analysis of these isolates show that these regions are confined to a pathogenic clade. CONCLUSION: Our data show that there is considerable genomic flux in this species and that the new highly virulent clone arose from an O3:K6 isolate that acquired at least seven novel regions, which included both a T3SS and a T6SS.
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spelling pubmed-24916232008-07-31 Molecular analysis of the emergence of pandemic Vibrio parahaemolyticus Boyd, E Fidelma Cohen, Ana Luisa V Naughton, Lynn M Ussery, David W Binnewies, Tim T Stine, O Colin Parent, Michelle A BMC Microbiol Research Article BACKGROUND: Vibrio parahaemolyticus is abundant in the aquatic environment particularly in warmer waters and is the leading cause of seafood borne gastroenteritis worldwide. Prior to 1995, numerous V. parahaemolyticus serogroups were associated with disease, however, in that year an O3:K6 serogroup emerged in Southeast Asia causing large outbreaks and rapid hospitalizations. This new highly virulent strain is now globally disseminated. RESULTS: We performed a four-way BLAST analysis on the genome sequence of V. parahaemolyticus RIMD2210633, an O3:K6 isolate from Japan recovered in 1996, versus the genomes of four published Vibrio species and constructed genome BLAST atlases. We identified 24 regions, gaps in the genome atlas, of greater than 10 kb that were unique to RIMD2210633. These 24 regions included an integron, f237 phage, 2 type III secretion systems (T3SS), a type VI secretion system (T6SS) and 7 Vibrio parahaemolyticus genomic islands (VPaI-1 to VPaI-7). Comparative genomic analysis of our fifth genome, V. parahaemolyticus AQ3810, an O3:K6 isolate recovered in 1983, identified four regions unique to each V. parahaemolyticus strain. Interestingly, AQ3810 did not encode 8 of the 24 regions unique to RMID, including a T6SS, which suggests an additional virulence mechanism in RIMD2210633. The distribution of only the VPaI regions was highly variable among a collection of 42 isolates and phylogenetic analysis of these isolates show that these regions are confined to a pathogenic clade. CONCLUSION: Our data show that there is considerable genomic flux in this species and that the new highly virulent clone arose from an O3:K6 isolate that acquired at least seven novel regions, which included both a T3SS and a T6SS. BioMed Central 2008-06-30 /pmc/articles/PMC2491623/ /pubmed/18590559 http://dx.doi.org/10.1186/1471-2180-8-110 Text en Copyright © 2008 Boyd 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
Boyd, E Fidelma
Cohen, Ana Luisa V
Naughton, Lynn M
Ussery, David W
Binnewies, Tim T
Stine, O Colin
Parent, Michelle A
Molecular analysis of the emergence of pandemic Vibrio parahaemolyticus
title Molecular analysis of the emergence of pandemic Vibrio parahaemolyticus
title_full Molecular analysis of the emergence of pandemic Vibrio parahaemolyticus
title_fullStr Molecular analysis of the emergence of pandemic Vibrio parahaemolyticus
title_full_unstemmed Molecular analysis of the emergence of pandemic Vibrio parahaemolyticus
title_short Molecular analysis of the emergence of pandemic Vibrio parahaemolyticus
title_sort molecular analysis of the emergence of pandemic vibrio parahaemolyticus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2491623/
https://www.ncbi.nlm.nih.gov/pubmed/18590559
http://dx.doi.org/10.1186/1471-2180-8-110
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