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Population analysis of Vibrio parahaemolyticus originating from different geographical regions demonstrates a high genetic diversity

BACKGROUND: Vibrio parahaemolyticus is frequently isolated from environmental and seafood samples and associated with gastroenteritis outbreakes in American, European, Asian and African countries. To distinguish between different lineages of V. parahaemolyticus various genotyping techniques have bee...

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Autores principales: Urmersbach, Sara, Alter, Thomas, Koralage, Madura Sanjeevani Gonsal, Sperling, Lisa, Gerdts, Gunnar, Messelhäusser, Ute, Huehn, Stephan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4015679/
https://www.ncbi.nlm.nih.gov/pubmed/24606756
http://dx.doi.org/10.1186/1471-2180-14-59
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author Urmersbach, Sara
Alter, Thomas
Koralage, Madura Sanjeevani Gonsal
Sperling, Lisa
Gerdts, Gunnar
Messelhäusser, Ute
Huehn, Stephan
author_facet Urmersbach, Sara
Alter, Thomas
Koralage, Madura Sanjeevani Gonsal
Sperling, Lisa
Gerdts, Gunnar
Messelhäusser, Ute
Huehn, Stephan
author_sort Urmersbach, Sara
collection PubMed
description BACKGROUND: Vibrio parahaemolyticus is frequently isolated from environmental and seafood samples and associated with gastroenteritis outbreakes in American, European, Asian and African countries. To distinguish between different lineages of V. parahaemolyticus various genotyping techniques have been used, incl. multilocus sequence typing (MLST). Even though some studies have already applied MLST analysis to characterize V. parahaemolyticus strain sets, these studies have been restricted to specific geographical areas (e.g. U.S. coast, Thailand and Peru), have focused exclusively on pandemic or non-pandemic pathogenic isolates or have been based on a limited strain number. RESULTS: To generate a global picture of V. parahaemolyticus genotype distribution, a collection of 130 environmental and seafood related V. parahaemolyticus isolates of different geographical origins (Sri Lanka, Ecuador, North Sea and Baltic Sea as well as German retail) was subjected to MLST analysis after modification of gyrB and recA PCRs. The V. parahaemolyticus population was composed of 82 unique Sequence Types (STs), of which 68 (82.9%) were new to the pubMLST database. After translating the in-frame nucleotide sequences into amino acid sequences, less diversity was detectable: a total of 31 different peptide Sequence Types (pSTs) with 19 (61.3%) new pSTs were generated from the analyzed isolates. Most STs did not show a global dissemination, but some were supra-regionally distributed and clusters of STs were dependent on geographical origin. On peptide level no general clustering of strains from specific geographical regions was observed, thereby the most common pSTs were found on all continents (Asia, South America and Europe) and rare pSTs were restricted to distinct countries or even geographical regions. One lineage of pSTs associated only with strains from North and Baltic Sea strains was identified. CONCLUSIONS: Our study reveals a high genetic diversity in the analyzed V. parahaemolyticus strain set as well as for geographical strain subsets, with a high proportion of newly discovered alleles and STs. Differences between the subsets were identified. Our data support the postulated population structure of V. parahaemolyticus which follows the ‘epidemic’ model of clonal expansion. Application of peptide based AA-MLST allowed the identification of reliable relationships between strains.
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spelling pubmed-40156792014-05-23 Population analysis of Vibrio parahaemolyticus originating from different geographical regions demonstrates a high genetic diversity Urmersbach, Sara Alter, Thomas Koralage, Madura Sanjeevani Gonsal Sperling, Lisa Gerdts, Gunnar Messelhäusser, Ute Huehn, Stephan BMC Microbiol Research Article BACKGROUND: Vibrio parahaemolyticus is frequently isolated from environmental and seafood samples and associated with gastroenteritis outbreakes in American, European, Asian and African countries. To distinguish between different lineages of V. parahaemolyticus various genotyping techniques have been used, incl. multilocus sequence typing (MLST). Even though some studies have already applied MLST analysis to characterize V. parahaemolyticus strain sets, these studies have been restricted to specific geographical areas (e.g. U.S. coast, Thailand and Peru), have focused exclusively on pandemic or non-pandemic pathogenic isolates or have been based on a limited strain number. RESULTS: To generate a global picture of V. parahaemolyticus genotype distribution, a collection of 130 environmental and seafood related V. parahaemolyticus isolates of different geographical origins (Sri Lanka, Ecuador, North Sea and Baltic Sea as well as German retail) was subjected to MLST analysis after modification of gyrB and recA PCRs. The V. parahaemolyticus population was composed of 82 unique Sequence Types (STs), of which 68 (82.9%) were new to the pubMLST database. After translating the in-frame nucleotide sequences into amino acid sequences, less diversity was detectable: a total of 31 different peptide Sequence Types (pSTs) with 19 (61.3%) new pSTs were generated from the analyzed isolates. Most STs did not show a global dissemination, but some were supra-regionally distributed and clusters of STs were dependent on geographical origin. On peptide level no general clustering of strains from specific geographical regions was observed, thereby the most common pSTs were found on all continents (Asia, South America and Europe) and rare pSTs were restricted to distinct countries or even geographical regions. One lineage of pSTs associated only with strains from North and Baltic Sea strains was identified. CONCLUSIONS: Our study reveals a high genetic diversity in the analyzed V. parahaemolyticus strain set as well as for geographical strain subsets, with a high proportion of newly discovered alleles and STs. Differences between the subsets were identified. Our data support the postulated population structure of V. parahaemolyticus which follows the ‘epidemic’ model of clonal expansion. Application of peptide based AA-MLST allowed the identification of reliable relationships between strains. BioMed Central 2014-03-08 /pmc/articles/PMC4015679/ /pubmed/24606756 http://dx.doi.org/10.1186/1471-2180-14-59 Text en Copyright © 2014 Urmersbach 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 credited. 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 Article
Urmersbach, Sara
Alter, Thomas
Koralage, Madura Sanjeevani Gonsal
Sperling, Lisa
Gerdts, Gunnar
Messelhäusser, Ute
Huehn, Stephan
Population analysis of Vibrio parahaemolyticus originating from different geographical regions demonstrates a high genetic diversity
title Population analysis of Vibrio parahaemolyticus originating from different geographical regions demonstrates a high genetic diversity
title_full Population analysis of Vibrio parahaemolyticus originating from different geographical regions demonstrates a high genetic diversity
title_fullStr Population analysis of Vibrio parahaemolyticus originating from different geographical regions demonstrates a high genetic diversity
title_full_unstemmed Population analysis of Vibrio parahaemolyticus originating from different geographical regions demonstrates a high genetic diversity
title_short Population analysis of Vibrio parahaemolyticus originating from different geographical regions demonstrates a high genetic diversity
title_sort population analysis of vibrio parahaemolyticus originating from different geographical regions demonstrates a high genetic diversity
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4015679/
https://www.ncbi.nlm.nih.gov/pubmed/24606756
http://dx.doi.org/10.1186/1471-2180-14-59
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