Rapid subtyping of pathogenic and nonpathogenic Vibrio parahaemolyticus by fourier transform infrared spectroscopy with chemometric analysis

Vibrio parahaemolyticus which naturally inhabits marine and estuarine environment represents pathogenic strains (virulence genes tdh or trh positive) and non-pathogenic strains (virulence genes negative). In this study, a rapid method for subtyping pathogenic and non-pathogenic V. parahaemolyticus w...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of microbiological methods 2018-12, Vol.155, p.70-77
Hauptverfasser: Li, Zhaojie, Chen, Shouguang, Xu, Chenggang, Ju, Lingyan, Li, Fengling
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 77
container_issue
container_start_page 70
container_title Journal of microbiological methods
container_volume 155
creator Li, Zhaojie
Chen, Shouguang
Xu, Chenggang
Ju, Lingyan
Li, Fengling
description Vibrio parahaemolyticus which naturally inhabits marine and estuarine environment represents pathogenic strains (virulence genes tdh or trh positive) and non-pathogenic strains (virulence genes negative). In this study, a rapid method for subtyping pathogenic and non-pathogenic V. parahaemolyticus was established using fourier transform infrared (FTIR) spectroscopy with chemometric analysis. This method targeted three strains of genotypes of V. parahaemolyticus including tdh positive, trh positive and virulence gene-negative (nonpathogenic) V. parahaemolyticus. The FTIR absorption spectra between 1800 and 900 cm−1 highlighted the most distinctive variations and were the most useful for characterizing the three bacteria. The successful differentiation and identification of the three bacteria could be accomplished in less than 1 h by FTIR using principal component analysis (PCA), or another cluster model of hierarchical cluster analysis (HCA). The method was verified by analyzing spiked V. parahaemolyticus fish samples. Furthermore, all of ten clinical isolates of V. parahaemolyticus were identified as tdh-positive, none of the clinical isolates were trh-positive, and all of ten environmental isolates were identified as non-pathogenic by the subtyping method, which were confirmed by PCR assays. All data demonstrated that the newly established subtyping method by FTIR is practical, time-saving, labor-saving, specific and cost-effective, especially suitable for the basic laboratories of CDC and port quarantine departments to perform suiveillance and epidemiological traceability of pathogenic V. parahaemolyticus. •A method for subtyping pathogenic V. parahaemolyticus was developed by FTIR with PCA or HCA.•The subtyping method targeted tdh+, trh+ and nonpathogenic V. parahaemolyticus.•A spectra database was constructed and used as reference to subtype the suspected bacteria.•The “fingerprints” characteristics of IR endow the subtyping method with high specificity.•The developed subtyping method is rapid and economical.
doi_str_mv 10.1016/j.mimet.2018.11.003
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2132286466</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0167701218306420</els_id><sourcerecordid>2132286466</sourcerecordid><originalsourceid>FETCH-LOGICAL-c359t-690db4a41f63897c1d4002e26214eee0496d0b39b0b037141b133bb2820bfe443</originalsourceid><addsrcrecordid>eNp9kc1q3TAQhUVpaW7SPkGhaNmN3RlJ8c-iixL6B4FASboVkjzO1cW2XMlu8Dv0oaPkpqWrrgTiO3NmzmHsDUKJgNX7Qzn6kZZSADYlYgkgn7EdNrUoGnnePme7TNVFDShO2GlKBwA8l6p5yU4kKFQKxI79_m5m3_G02mWb_XTLQ89ns-zDLU3ecTN1fArTPz8_vI0-ZCaavaExDNvi3Zq43Xgf1ugp8iWaKfUhjtxPfTSR8vyZ3BJDcmHe-J1f9tztszivHx9dzLAln16xF70ZEr1-es_YzedP1xdfi8urL98uPl4WLt-1FFULnVVGYV_Jpq0ddgpAkKgEKiIC1VYdWNlasCBrVGhRSmtFI8D2pJQ8Y--Oc-cYfq6UFj365GgYzERhTVqgFKKpVFVlVB5Rl7dPkXo9Rz-auGkE_VCDPujHGvRDDRpR5xqy6u2TwWpH6v5q_uSegQ9HgPKZv3JoOjlPk6POx5yU7oL_r8E94Amdjg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2132286466</pqid></control><display><type>article</type><title>Rapid subtyping of pathogenic and nonpathogenic Vibrio parahaemolyticus by fourier transform infrared spectroscopy with chemometric analysis</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals Complete</source><creator>Li, Zhaojie ; Chen, Shouguang ; Xu, Chenggang ; Ju, Lingyan ; Li, Fengling</creator><creatorcontrib>Li, Zhaojie ; Chen, Shouguang ; Xu, Chenggang ; Ju, Lingyan ; Li, Fengling</creatorcontrib><description>Vibrio parahaemolyticus which naturally inhabits marine and estuarine environment represents pathogenic strains (virulence genes tdh or trh positive) and non-pathogenic strains (virulence genes negative). In this study, a rapid method for subtyping pathogenic and non-pathogenic V. parahaemolyticus was established using fourier transform infrared (FTIR) spectroscopy with chemometric analysis. This method targeted three strains of genotypes of V. parahaemolyticus including tdh positive, trh positive and virulence gene-negative (nonpathogenic) V. parahaemolyticus. The FTIR absorption spectra between 1800 and 900 cm−1 highlighted the most distinctive variations and were the most useful for characterizing the three bacteria. The successful differentiation and identification of the three bacteria could be accomplished in less than 1 h by FTIR using principal component analysis (PCA), or another cluster model of hierarchical cluster analysis (HCA). The method was verified by analyzing spiked V. parahaemolyticus fish samples. Furthermore, all of ten clinical isolates of V. parahaemolyticus were identified as tdh-positive, none of the clinical isolates were trh-positive, and all of ten environmental isolates were identified as non-pathogenic by the subtyping method, which were confirmed by PCR assays. All data demonstrated that the newly established subtyping method by FTIR is practical, time-saving, labor-saving, specific and cost-effective, especially suitable for the basic laboratories of CDC and port quarantine departments to perform suiveillance and epidemiological traceability of pathogenic V. parahaemolyticus. •A method for subtyping pathogenic V. parahaemolyticus was developed by FTIR with PCA or HCA.•The subtyping method targeted tdh+, trh+ and nonpathogenic V. parahaemolyticus.•A spectra database was constructed and used as reference to subtype the suspected bacteria.•The “fingerprints” characteristics of IR endow the subtyping method with high specificity.•The developed subtyping method is rapid and economical.</description><identifier>ISSN: 0167-7012</identifier><identifier>EISSN: 1872-8359</identifier><identifier>DOI: 10.1016/j.mimet.2018.11.003</identifier><identifier>PMID: 30414402</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Animals ; Bacterial Proteins - genetics ; Bacterial Typing Techniques - methods ; Cluster Analysis ; DNA Fingerprinting ; Environmental Microbiology ; Fishes - microbiology ; Fourier transform infrared spectroscopy ; Genotype ; Genotyping Techniques - methods ; Hierarchical cluster analysis ; Pathogenicity ; Polymerase Chain Reaction - methods ; Principal component analysis ; Seafood - microbiology ; Spectroscopy, Fourier Transform Infrared - methods ; Subtype ; Vibrio Infections - microbiology ; Vibrio parahaemolyticus ; Vibrio parahaemolyticus - classification ; Vibrio parahaemolyticus - genetics ; Vibrio parahaemolyticus - isolation &amp; purification ; Vibrio parahaemolyticus - pathogenicity ; Virulence - genetics ; Virulence Factors - genetics</subject><ispartof>Journal of microbiological methods, 2018-12, Vol.155, p.70-77</ispartof><rights>2018 Elsevier B.V.</rights><rights>Copyright © 2018 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c359t-690db4a41f63897c1d4002e26214eee0496d0b39b0b037141b133bb2820bfe443</citedby><cites>FETCH-LOGICAL-c359t-690db4a41f63897c1d4002e26214eee0496d0b39b0b037141b133bb2820bfe443</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.mimet.2018.11.003$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27928,27929,45999</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30414402$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Zhaojie</creatorcontrib><creatorcontrib>Chen, Shouguang</creatorcontrib><creatorcontrib>Xu, Chenggang</creatorcontrib><creatorcontrib>Ju, Lingyan</creatorcontrib><creatorcontrib>Li, Fengling</creatorcontrib><title>Rapid subtyping of pathogenic and nonpathogenic Vibrio parahaemolyticus by fourier transform infrared spectroscopy with chemometric analysis</title><title>Journal of microbiological methods</title><addtitle>J Microbiol Methods</addtitle><description>Vibrio parahaemolyticus which naturally inhabits marine and estuarine environment represents pathogenic strains (virulence genes tdh or trh positive) and non-pathogenic strains (virulence genes negative). In this study, a rapid method for subtyping pathogenic and non-pathogenic V. parahaemolyticus was established using fourier transform infrared (FTIR) spectroscopy with chemometric analysis. This method targeted three strains of genotypes of V. parahaemolyticus including tdh positive, trh positive and virulence gene-negative (nonpathogenic) V. parahaemolyticus. The FTIR absorption spectra between 1800 and 900 cm−1 highlighted the most distinctive variations and were the most useful for characterizing the three bacteria. The successful differentiation and identification of the three bacteria could be accomplished in less than 1 h by FTIR using principal component analysis (PCA), or another cluster model of hierarchical cluster analysis (HCA). The method was verified by analyzing spiked V. parahaemolyticus fish samples. Furthermore, all of ten clinical isolates of V. parahaemolyticus were identified as tdh-positive, none of the clinical isolates were trh-positive, and all of ten environmental isolates were identified as non-pathogenic by the subtyping method, which were confirmed by PCR assays. All data demonstrated that the newly established subtyping method by FTIR is practical, time-saving, labor-saving, specific and cost-effective, especially suitable for the basic laboratories of CDC and port quarantine departments to perform suiveillance and epidemiological traceability of pathogenic V. parahaemolyticus. •A method for subtyping pathogenic V. parahaemolyticus was developed by FTIR with PCA or HCA.•The subtyping method targeted tdh+, trh+ and nonpathogenic V. parahaemolyticus.•A spectra database was constructed and used as reference to subtype the suspected bacteria.•The “fingerprints” characteristics of IR endow the subtyping method with high specificity.•The developed subtyping method is rapid and economical.</description><subject>Animals</subject><subject>Bacterial Proteins - genetics</subject><subject>Bacterial Typing Techniques - methods</subject><subject>Cluster Analysis</subject><subject>DNA Fingerprinting</subject><subject>Environmental Microbiology</subject><subject>Fishes - microbiology</subject><subject>Fourier transform infrared spectroscopy</subject><subject>Genotype</subject><subject>Genotyping Techniques - methods</subject><subject>Hierarchical cluster analysis</subject><subject>Pathogenicity</subject><subject>Polymerase Chain Reaction - methods</subject><subject>Principal component analysis</subject><subject>Seafood - microbiology</subject><subject>Spectroscopy, Fourier Transform Infrared - methods</subject><subject>Subtype</subject><subject>Vibrio Infections - microbiology</subject><subject>Vibrio parahaemolyticus</subject><subject>Vibrio parahaemolyticus - classification</subject><subject>Vibrio parahaemolyticus - genetics</subject><subject>Vibrio parahaemolyticus - isolation &amp; purification</subject><subject>Vibrio parahaemolyticus - pathogenicity</subject><subject>Virulence - genetics</subject><subject>Virulence Factors - genetics</subject><issn>0167-7012</issn><issn>1872-8359</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kc1q3TAQhUVpaW7SPkGhaNmN3RlJ8c-iixL6B4FASboVkjzO1cW2XMlu8Dv0oaPkpqWrrgTiO3NmzmHsDUKJgNX7Qzn6kZZSADYlYgkgn7EdNrUoGnnePme7TNVFDShO2GlKBwA8l6p5yU4kKFQKxI79_m5m3_G02mWb_XTLQ89ns-zDLU3ecTN1fArTPz8_vI0-ZCaavaExDNvi3Zq43Xgf1ugp8iWaKfUhjtxPfTSR8vyZ3BJDcmHe-J1f9tztszivHx9dzLAln16xF70ZEr1-es_YzedP1xdfi8urL98uPl4WLt-1FFULnVVGYV_Jpq0ddgpAkKgEKiIC1VYdWNlasCBrVGhRSmtFI8D2pJQ8Y--Oc-cYfq6UFj365GgYzERhTVqgFKKpVFVlVB5Rl7dPkXo9Rz-auGkE_VCDPujHGvRDDRpR5xqy6u2TwWpH6v5q_uSegQ9HgPKZv3JoOjlPk6POx5yU7oL_r8E94Amdjg</recordid><startdate>201812</startdate><enddate>201812</enddate><creator>Li, Zhaojie</creator><creator>Chen, Shouguang</creator><creator>Xu, Chenggang</creator><creator>Ju, Lingyan</creator><creator>Li, Fengling</creator><general>Elsevier B.V</general><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></search><sort><creationdate>201812</creationdate><title>Rapid subtyping of pathogenic and nonpathogenic Vibrio parahaemolyticus by fourier transform infrared spectroscopy with chemometric analysis</title><author>Li, Zhaojie ; Chen, Shouguang ; Xu, Chenggang ; Ju, Lingyan ; Li, Fengling</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c359t-690db4a41f63897c1d4002e26214eee0496d0b39b0b037141b133bb2820bfe443</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Animals</topic><topic>Bacterial Proteins - genetics</topic><topic>Bacterial Typing Techniques - methods</topic><topic>Cluster Analysis</topic><topic>DNA Fingerprinting</topic><topic>Environmental Microbiology</topic><topic>Fishes - microbiology</topic><topic>Fourier transform infrared spectroscopy</topic><topic>Genotype</topic><topic>Genotyping Techniques - methods</topic><topic>Hierarchical cluster analysis</topic><topic>Pathogenicity</topic><topic>Polymerase Chain Reaction - methods</topic><topic>Principal component analysis</topic><topic>Seafood - microbiology</topic><topic>Spectroscopy, Fourier Transform Infrared - methods</topic><topic>Subtype</topic><topic>Vibrio Infections - microbiology</topic><topic>Vibrio parahaemolyticus</topic><topic>Vibrio parahaemolyticus - classification</topic><topic>Vibrio parahaemolyticus - genetics</topic><topic>Vibrio parahaemolyticus - isolation &amp; purification</topic><topic>Vibrio parahaemolyticus - pathogenicity</topic><topic>Virulence - genetics</topic><topic>Virulence Factors - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Zhaojie</creatorcontrib><creatorcontrib>Chen, Shouguang</creatorcontrib><creatorcontrib>Xu, Chenggang</creatorcontrib><creatorcontrib>Ju, Lingyan</creatorcontrib><creatorcontrib>Li, Fengling</creatorcontrib><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><jtitle>Journal of microbiological methods</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Zhaojie</au><au>Chen, Shouguang</au><au>Xu, Chenggang</au><au>Ju, Lingyan</au><au>Li, Fengling</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rapid subtyping of pathogenic and nonpathogenic Vibrio parahaemolyticus by fourier transform infrared spectroscopy with chemometric analysis</atitle><jtitle>Journal of microbiological methods</jtitle><addtitle>J Microbiol Methods</addtitle><date>2018-12</date><risdate>2018</risdate><volume>155</volume><spage>70</spage><epage>77</epage><pages>70-77</pages><issn>0167-7012</issn><eissn>1872-8359</eissn><abstract>Vibrio parahaemolyticus which naturally inhabits marine and estuarine environment represents pathogenic strains (virulence genes tdh or trh positive) and non-pathogenic strains (virulence genes negative). In this study, a rapid method for subtyping pathogenic and non-pathogenic V. parahaemolyticus was established using fourier transform infrared (FTIR) spectroscopy with chemometric analysis. This method targeted three strains of genotypes of V. parahaemolyticus including tdh positive, trh positive and virulence gene-negative (nonpathogenic) V. parahaemolyticus. The FTIR absorption spectra between 1800 and 900 cm−1 highlighted the most distinctive variations and were the most useful for characterizing the three bacteria. The successful differentiation and identification of the three bacteria could be accomplished in less than 1 h by FTIR using principal component analysis (PCA), or another cluster model of hierarchical cluster analysis (HCA). The method was verified by analyzing spiked V. parahaemolyticus fish samples. Furthermore, all of ten clinical isolates of V. parahaemolyticus were identified as tdh-positive, none of the clinical isolates were trh-positive, and all of ten environmental isolates were identified as non-pathogenic by the subtyping method, which were confirmed by PCR assays. All data demonstrated that the newly established subtyping method by FTIR is practical, time-saving, labor-saving, specific and cost-effective, especially suitable for the basic laboratories of CDC and port quarantine departments to perform suiveillance and epidemiological traceability of pathogenic V. parahaemolyticus. •A method for subtyping pathogenic V. parahaemolyticus was developed by FTIR with PCA or HCA.•The subtyping method targeted tdh+, trh+ and nonpathogenic V. parahaemolyticus.•A spectra database was constructed and used as reference to subtype the suspected bacteria.•The “fingerprints” characteristics of IR endow the subtyping method with high specificity.•The developed subtyping method is rapid and economical.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>30414402</pmid><doi>10.1016/j.mimet.2018.11.003</doi><tpages>8</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0167-7012
ispartof Journal of microbiological methods, 2018-12, Vol.155, p.70-77
issn 0167-7012
1872-8359
language eng
recordid cdi_proquest_miscellaneous_2132286466
source MEDLINE; Elsevier ScienceDirect Journals Complete
subjects Animals
Bacterial Proteins - genetics
Bacterial Typing Techniques - methods
Cluster Analysis
DNA Fingerprinting
Environmental Microbiology
Fishes - microbiology
Fourier transform infrared spectroscopy
Genotype
Genotyping Techniques - methods
Hierarchical cluster analysis
Pathogenicity
Polymerase Chain Reaction - methods
Principal component analysis
Seafood - microbiology
Spectroscopy, Fourier Transform Infrared - methods
Subtype
Vibrio Infections - microbiology
Vibrio parahaemolyticus
Vibrio parahaemolyticus - classification
Vibrio parahaemolyticus - genetics
Vibrio parahaemolyticus - isolation & purification
Vibrio parahaemolyticus - pathogenicity
Virulence - genetics
Virulence Factors - genetics
title Rapid subtyping of pathogenic and nonpathogenic Vibrio parahaemolyticus by fourier transform infrared spectroscopy with chemometric analysis
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-17T08%3A05%3A54IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Rapid%20subtyping%20of%20pathogenic%20and%20nonpathogenic%20Vibrio%20parahaemolyticus%20by%20fourier%20transform%20infrared%20spectroscopy%20with%20chemometric%20analysis&rft.jtitle=Journal%20of%20microbiological%20methods&rft.au=Li,%20Zhaojie&rft.date=2018-12&rft.volume=155&rft.spage=70&rft.epage=77&rft.pages=70-77&rft.issn=0167-7012&rft.eissn=1872-8359&rft_id=info:doi/10.1016/j.mimet.2018.11.003&rft_dat=%3Cproquest_cross%3E2132286466%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2132286466&rft_id=info:pmid/30414402&rft_els_id=S0167701218306420&rfr_iscdi=true