Molecular characterization of clinical and environmental Vibrio parahaemolyticus isolates in Taiwan
Vibrio parahaemolyticus is the most prevalent foodborne pathogen in Taiwan and it is frequently recovered from seafood. In this study, V. parahaemolyticus that was isolated in recent years from aquacultural environments and clinical specimens were comparatively analyzed by NotI-restricted pulsed-fie...
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description | Vibrio parahaemolyticus is the most prevalent foodborne pathogen in Taiwan and it is frequently recovered from seafood. In this study, V. parahaemolyticus that was isolated in recent years from aquacultural environments and clinical specimens were comparatively analyzed by NotI-restricted pulsed-field gel electrophoresis (PFGE) and polymerase chain reaction, targeting common toxin genes (tdh, trh, ureC), MTase gene, toxR regulator, markers for pandemic strains (ORF8, group-specific toxRS) and representative genes of type three secretion systems T3SS1 (vcrD1, VP1680, vopD) and T3SS2α (vcrD2, vopD2, vopB2, vopP, vopC, vopT). Among the 48 clinical isolates and 93 environmental isolates that were analyzed by PFGE, a total of 26 and 76 pulsetypes were identified and grouped into six and nine clusters, respectively, at 80% similarity. The pandemic O3:K6 clones and other clinical and environmental isolates were further characterized according to the distribution of these examined target genes. The MTase gene and the vopB2, vopP, vopC and vopT genes of T3SS2α were present at a significantly higher frequency (>90%) in the pandemic clones than in other clinical isolates. The MTase gene and some other virulence-associated genes were also present in a few of the environmental isolates, and these results suggest the horizontal transfer of these genes in the clinical and environmental isolates of this species.
•First to characterize environmental/clinical isolates of V. parahaemolyticus in Taiwan•PFGE clusters indicate phylogenetic relatedness of environmental/clinical isolates.•Isolates further characterized/grouped by profiles of virulence-associated genes•T3SS2α and MTase genes were found in most pandemic isolates, and in a few environmental isolates. |
doi_str_mv | 10.1016/j.ijfoodmicro.2013.04.017 |
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•First to characterize environmental/clinical isolates of V. parahaemolyticus in Taiwan•PFGE clusters indicate phylogenetic relatedness of environmental/clinical isolates.•Isolates further characterized/grouped by profiles of virulence-associated genes•T3SS2α and MTase genes were found in most pandemic isolates, and in a few environmental isolates.</description><identifier>ISSN: 0168-1605</identifier><identifier>EISSN: 1879-3460</identifier><identifier>DOI: 10.1016/j.ijfoodmicro.2013.04.017</identifier><identifier>PMID: 23685468</identifier><identifier>CODEN: IJFMDD</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Animals ; Aquaculture ; Biological and medical sciences ; Electrophoresis, Gel, Pulsed-Field ; Environmental Microbiology ; Food industries ; Food microbiology ; Fundamental and applied biological sciences. Psychology ; Gene Transfer, Horizontal ; Humans ; MTase ; PFGE ; Phylogeny ; Polymerase Chain Reaction ; T3SS2α ; Taiwan ; Vibrio Infections - microbiology ; Vibrio parahaemolyticus ; Vibrio parahaemolyticus - classification ; Vibrio parahaemolyticus - genetics ; Vibrio parahaemolyticus - isolation & purification ; Virulence ; Virulence Factors - genetics</subject><ispartof>International journal of food microbiology, 2013-07, Vol.165 (1), p.18-26</ispartof><rights>2013 Elsevier B.V.</rights><rights>2014 INIST-CNRS</rights><rights>Copyright © 2013 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c440t-8695c1c1bfd8b13218133eb1a109fc3d25957e341fffbd4d0dd542eefff3a53a3</citedby><cites>FETCH-LOGICAL-c440t-8695c1c1bfd8b13218133eb1a109fc3d25957e341fffbd4d0dd542eefff3a53a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ijfoodmicro.2013.04.017$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=27461616$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23685468$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tsai, Shing-en</creatorcontrib><creatorcontrib>Jong, Koa-Jen</creatorcontrib><creatorcontrib>Tey, Yao Hsien</creatorcontrib><creatorcontrib>Yu, Wei-Ting</creatorcontrib><creatorcontrib>Chiou, Chien-Shun</creatorcontrib><creatorcontrib>Lee, Yeong-Sheng</creatorcontrib><creatorcontrib>Wong, Hin-chung</creatorcontrib><title>Molecular characterization of clinical and environmental Vibrio parahaemolyticus isolates in Taiwan</title><title>International journal of food microbiology</title><addtitle>Int J Food Microbiol</addtitle><description>Vibrio parahaemolyticus is the most prevalent foodborne pathogen in Taiwan and it is frequently recovered from seafood. In this study, V. parahaemolyticus that was isolated in recent years from aquacultural environments and clinical specimens were comparatively analyzed by NotI-restricted pulsed-field gel electrophoresis (PFGE) and polymerase chain reaction, targeting common toxin genes (tdh, trh, ureC), MTase gene, toxR regulator, markers for pandemic strains (ORF8, group-specific toxRS) and representative genes of type three secretion systems T3SS1 (vcrD1, VP1680, vopD) and T3SS2α (vcrD2, vopD2, vopB2, vopP, vopC, vopT). Among the 48 clinical isolates and 93 environmental isolates that were analyzed by PFGE, a total of 26 and 76 pulsetypes were identified and grouped into six and nine clusters, respectively, at 80% similarity. The pandemic O3:K6 clones and other clinical and environmental isolates were further characterized according to the distribution of these examined target genes. The MTase gene and the vopB2, vopP, vopC and vopT genes of T3SS2α were present at a significantly higher frequency (>90%) in the pandemic clones than in other clinical isolates. The MTase gene and some other virulence-associated genes were also present in a few of the environmental isolates, and these results suggest the horizontal transfer of these genes in the clinical and environmental isolates of this species.
•First to characterize environmental/clinical isolates of V. parahaemolyticus in Taiwan•PFGE clusters indicate phylogenetic relatedness of environmental/clinical isolates.•Isolates further characterized/grouped by profiles of virulence-associated genes•T3SS2α and MTase genes were found in most pandemic isolates, and in a few environmental isolates.</description><subject>Animals</subject><subject>Aquaculture</subject><subject>Biological and medical sciences</subject><subject>Electrophoresis, Gel, Pulsed-Field</subject><subject>Environmental Microbiology</subject><subject>Food industries</subject><subject>Food microbiology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene Transfer, Horizontal</subject><subject>Humans</subject><subject>MTase</subject><subject>PFGE</subject><subject>Phylogeny</subject><subject>Polymerase Chain Reaction</subject><subject>T3SS2α</subject><subject>Taiwan</subject><subject>Vibrio Infections - microbiology</subject><subject>Vibrio parahaemolyticus</subject><subject>Vibrio parahaemolyticus - classification</subject><subject>Vibrio parahaemolyticus - genetics</subject><subject>Vibrio parahaemolyticus - isolation & purification</subject><subject>Virulence</subject><subject>Virulence Factors - genetics</subject><issn>0168-1605</issn><issn>1879-3460</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkUmP1DAQRi0EYpqBv4DCAYlLgiu2sxxRi00axGXgajl2WVOtxG7sZNDw6_Gom-U48sGLXpVL72PsFfAGOHRvDw0dfIxuIZti03IQDZcNh_4R28HQj7WQHX_MdoUdaui4umDPcj5wzpUQ_Cm7aEU3KNkNO2a_xBntNptU2RuTjF0x0S-zUgxV9JWdKZA1c2WCqzDcUophwbCWl-80JYrVsRTdGFzifLeS3XJFOc5mxXII1bWhnyY8Z0-8mTO-OO-X7NuH99f7T_XV14-f9--uaislX-uhG5UFC5N3wwSihQGEwAkM8NFb4Vo1qh6FBO_95KTjzinZIparMEoYccnenPoeU_yxYV71QtniPJuAccsaRN8WA33bPwBVZRpVLBV0PKHFdc4JvT4mWky608D1fRz6oP-LQ9_HobnUJY5S-_L8zTYt6P5W_vFfgNdnwOSi2ScTLOV_XC87KKtw-xOHxd8tYdLZEgaLjhLaVbtIDxjnNzbQsOc</recordid><startdate>20130701</startdate><enddate>20130701</enddate><creator>Tsai, Shing-en</creator><creator>Jong, Koa-Jen</creator><creator>Tey, Yao Hsien</creator><creator>Yu, Wei-Ting</creator><creator>Chiou, Chien-Shun</creator><creator>Lee, Yeong-Sheng</creator><creator>Wong, Hin-chung</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7QL</scope><scope>7T7</scope><scope>7TN</scope><scope>8FD</scope><scope>C1K</scope><scope>F1W</scope><scope>FR3</scope><scope>H95</scope><scope>H98</scope><scope>L.G</scope><scope>P64</scope></search><sort><creationdate>20130701</creationdate><title>Molecular characterization of clinical and environmental Vibrio parahaemolyticus isolates in Taiwan</title><author>Tsai, Shing-en ; Jong, Koa-Jen ; Tey, Yao Hsien ; Yu, Wei-Ting ; Chiou, Chien-Shun ; Lee, Yeong-Sheng ; Wong, Hin-chung</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c440t-8695c1c1bfd8b13218133eb1a109fc3d25957e341fffbd4d0dd542eefff3a53a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Animals</topic><topic>Aquaculture</topic><topic>Biological and medical sciences</topic><topic>Electrophoresis, Gel, Pulsed-Field</topic><topic>Environmental Microbiology</topic><topic>Food industries</topic><topic>Food microbiology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene Transfer, Horizontal</topic><topic>Humans</topic><topic>MTase</topic><topic>PFGE</topic><topic>Phylogeny</topic><topic>Polymerase Chain Reaction</topic><topic>T3SS2α</topic><topic>Taiwan</topic><topic>Vibrio Infections - microbiology</topic><topic>Vibrio parahaemolyticus</topic><topic>Vibrio parahaemolyticus - classification</topic><topic>Vibrio parahaemolyticus - genetics</topic><topic>Vibrio parahaemolyticus - isolation & purification</topic><topic>Virulence</topic><topic>Virulence Factors - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tsai, Shing-en</creatorcontrib><creatorcontrib>Jong, Koa-Jen</creatorcontrib><creatorcontrib>Tey, Yao Hsien</creatorcontrib><creatorcontrib>Yu, Wei-Ting</creatorcontrib><creatorcontrib>Chiou, Chien-Shun</creatorcontrib><creatorcontrib>Lee, Yeong-Sheng</creatorcontrib><creatorcontrib>Wong, Hin-chung</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Oceanic Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Engineering Research Database</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Aquaculture Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>International journal of food microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tsai, Shing-en</au><au>Jong, Koa-Jen</au><au>Tey, Yao Hsien</au><au>Yu, Wei-Ting</au><au>Chiou, Chien-Shun</au><au>Lee, Yeong-Sheng</au><au>Wong, Hin-chung</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Molecular characterization of clinical and environmental Vibrio parahaemolyticus isolates in Taiwan</atitle><jtitle>International journal of food microbiology</jtitle><addtitle>Int J Food Microbiol</addtitle><date>2013-07-01</date><risdate>2013</risdate><volume>165</volume><issue>1</issue><spage>18</spage><epage>26</epage><pages>18-26</pages><issn>0168-1605</issn><eissn>1879-3460</eissn><coden>IJFMDD</coden><abstract>Vibrio parahaemolyticus is the most prevalent foodborne pathogen in Taiwan and it is frequently recovered from seafood. In this study, V. parahaemolyticus that was isolated in recent years from aquacultural environments and clinical specimens were comparatively analyzed by NotI-restricted pulsed-field gel electrophoresis (PFGE) and polymerase chain reaction, targeting common toxin genes (tdh, trh, ureC), MTase gene, toxR regulator, markers for pandemic strains (ORF8, group-specific toxRS) and representative genes of type three secretion systems T3SS1 (vcrD1, VP1680, vopD) and T3SS2α (vcrD2, vopD2, vopB2, vopP, vopC, vopT). Among the 48 clinical isolates and 93 environmental isolates that were analyzed by PFGE, a total of 26 and 76 pulsetypes were identified and grouped into six and nine clusters, respectively, at 80% similarity. The pandemic O3:K6 clones and other clinical and environmental isolates were further characterized according to the distribution of these examined target genes. The MTase gene and the vopB2, vopP, vopC and vopT genes of T3SS2α were present at a significantly higher frequency (>90%) in the pandemic clones than in other clinical isolates. The MTase gene and some other virulence-associated genes were also present in a few of the environmental isolates, and these results suggest the horizontal transfer of these genes in the clinical and environmental isolates of this species.
•First to characterize environmental/clinical isolates of V. parahaemolyticus in Taiwan•PFGE clusters indicate phylogenetic relatedness of environmental/clinical isolates.•Isolates further characterized/grouped by profiles of virulence-associated genes•T3SS2α and MTase genes were found in most pandemic isolates, and in a few environmental isolates.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>23685468</pmid><doi>10.1016/j.ijfoodmicro.2013.04.017</doi><tpages>9</tpages></addata></record> |
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subjects | Animals Aquaculture Biological and medical sciences Electrophoresis, Gel, Pulsed-Field Environmental Microbiology Food industries Food microbiology Fundamental and applied biological sciences. Psychology Gene Transfer, Horizontal Humans MTase PFGE Phylogeny Polymerase Chain Reaction T3SS2α Taiwan Vibrio Infections - microbiology Vibrio parahaemolyticus Vibrio parahaemolyticus - classification Vibrio parahaemolyticus - genetics Vibrio parahaemolyticus - isolation & purification Virulence Virulence Factors - genetics |
title | Molecular characterization of clinical and environmental Vibrio parahaemolyticus isolates in Taiwan |
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