Loading…
Fluorometric method for enumeration of Escherichia coli in molluscan shellfish
A novel procedure for enumerating Escherichia coli in molluscan shellfish has been developed and evaluated. The method, a singular modification of the APHA most probable number (MPN) procedure, incorporates a fluorogenic molecule, 4-methylumbelliferyl-β-D-glucuronide (MUG), into the confirmed medium...
Saved in:
Published in: | Journal of food protection 1987-08, Vol.50 (8), p.685-690 |
---|---|
Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c396t-459b791ca55514d55edb8d736ff8a45ceeeb4cd5fc502baa00f4614a3f8475893 |
---|---|
cites | |
container_end_page | 690 |
container_issue | 8 |
container_start_page | 685 |
container_title | Journal of food protection |
container_volume | 50 |
creator | Rippey, S.R Chandler, L.A Watkins, W.D |
description | A novel procedure for enumerating Escherichia coli in molluscan shellfish has been developed and evaluated. The method, a singular modification of the APHA most probable number (MPN) procedure, incorporates a fluorogenic molecule, 4-methylumbelliferyl-β-D-glucuronide (MUG), into the confirmed medium (EC) at a concentration of 50 μg/ml. The substrate could not be incorporated into the presumptive medium (LST) because of fluorescence resulting from the shellfish tissues themselves. After incubation, tubes were examined for fluorescence under long-wave ultraviolet light. Fluorescence indicated presence of E. coli . Of 1151 EC tubes examined for E. coli , both positive and negative for fluorescence, the confirmed positive rate was 91% and the false-negative rate was 11%. Certain problems inherent to the classical MPN procedure itself may understate and overstate these rates, respectively. Of more than 500 E. coli and non- E. coli isolates examined for β-glucuronidase activity, 95% of the E. coli isolates were positive for this enzyme, and only one non- E. coli isolate (a Shigella species) produced the enzyme. The MUG method, which requires only 48 h for enumeration of E. coli in shellfish, provides a considerable saving in time and labor over the standard APHA MPN procedure. |
doi_str_mv | 10.4315/0362-028x-50.8.685 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2207169365</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2207169365</sourcerecordid><originalsourceid>FETCH-LOGICAL-c396t-459b791ca55514d55edb8d736ff8a45ceeeb4cd5fc502baa00f4614a3f8475893</originalsourceid><addsrcrecordid>eNo90D1PHDEQgGELBcFx4Q-kSFykoNnL-HPtMkJAIp2gSJDoLK_XzjraXRP7ViL_Hp_uwM00z4ysF6FPBDacEfENmKQNUPXSCNiojVTiBK2I5rzRoNsPaPUGns7RRSl_AYBqKs_QOQMtBW_JCt3fjkvKafK7HB2uY0g9DiljPy-Tz3YX04xTwDfFDb6SIVrs0hhxnPGUxnEpzs64DH4cQyzDR3Qa7Fj85XGu0ePtze_rH8324e7n9fdt45iWu4YL3bWaOCuEILwXwved6lsmQ1CWC-e977jrRXACaGctQOCScMuC4q1Qmq3R1eHuc07_Fl92ZorF1U_Y2aelGEqhJVIzKSqlB-pyKiX7YJ5znGz-bwiYfUezz2T2mYwAo0ztWJc-H-8v3eT795W3cBV8PQJbC4wh29nF8u4U1aS-yr4cWLDJ2D-5ksdfFAgDwhkwRdkrCrKEqQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2207169365</pqid></control><display><type>article</type><title>Fluorometric method for enumeration of Escherichia coli in molluscan shellfish</title><source>ScienceDirect Additional Titles</source><creator>Rippey, S.R ; Chandler, L.A ; Watkins, W.D</creator><creatorcontrib>Rippey, S.R ; Chandler, L.A ; Watkins, W.D</creatorcontrib><description>A novel procedure for enumerating Escherichia coli in molluscan shellfish has been developed and evaluated. The method, a singular modification of the APHA most probable number (MPN) procedure, incorporates a fluorogenic molecule, 4-methylumbelliferyl-β-D-glucuronide (MUG), into the confirmed medium (EC) at a concentration of 50 μg/ml. The substrate could not be incorporated into the presumptive medium (LST) because of fluorescence resulting from the shellfish tissues themselves. After incubation, tubes were examined for fluorescence under long-wave ultraviolet light. Fluorescence indicated presence of E. coli . Of 1151 EC tubes examined for E. coli , both positive and negative for fluorescence, the confirmed positive rate was 91% and the false-negative rate was 11%. Certain problems inherent to the classical MPN procedure itself may understate and overstate these rates, respectively. Of more than 500 E. coli and non- E. coli isolates examined for β-glucuronidase activity, 95% of the E. coli isolates were positive for this enzyme, and only one non- E. coli isolate (a Shigella species) produced the enzyme. The MUG method, which requires only 48 h for enumeration of E. coli in shellfish, provides a considerable saving in time and labor over the standard APHA MPN procedure.</description><identifier>ISSN: 0362-028X</identifier><identifier>EISSN: 1944-9097</identifier><identifier>DOI: 10.4315/0362-028x-50.8.685</identifier><identifier>PMID: 30965471</identifier><identifier>CODEN: JFPRDR</identifier><language>eng</language><publisher>Des Moines, IA: International Association of Milk, Food and Environmental Sanitarians</publisher><subject>Biological and medical sciences ; enumeration ; Escherichia coli ; Fish and seafood industries ; fluorimetry ; Food industries ; food sanitation ; Fundamental and applied biological sciences. Psychology ; molluscs</subject><ispartof>Journal of food protection, 1987-08, Vol.50 (8), p.685-690</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c396t-459b791ca55514d55edb8d736ff8a45ceeeb4cd5fc502baa00f4614a3f8475893</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=8291111$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30965471$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rippey, S.R</creatorcontrib><creatorcontrib>Chandler, L.A</creatorcontrib><creatorcontrib>Watkins, W.D</creatorcontrib><title>Fluorometric method for enumeration of Escherichia coli in molluscan shellfish</title><title>Journal of food protection</title><addtitle>J Food Prot</addtitle><description>A novel procedure for enumerating Escherichia coli in molluscan shellfish has been developed and evaluated. The method, a singular modification of the APHA most probable number (MPN) procedure, incorporates a fluorogenic molecule, 4-methylumbelliferyl-β-D-glucuronide (MUG), into the confirmed medium (EC) at a concentration of 50 μg/ml. The substrate could not be incorporated into the presumptive medium (LST) because of fluorescence resulting from the shellfish tissues themselves. After incubation, tubes were examined for fluorescence under long-wave ultraviolet light. Fluorescence indicated presence of E. coli . Of 1151 EC tubes examined for E. coli , both positive and negative for fluorescence, the confirmed positive rate was 91% and the false-negative rate was 11%. Certain problems inherent to the classical MPN procedure itself may understate and overstate these rates, respectively. Of more than 500 E. coli and non- E. coli isolates examined for β-glucuronidase activity, 95% of the E. coli isolates were positive for this enzyme, and only one non- E. coli isolate (a Shigella species) produced the enzyme. The MUG method, which requires only 48 h for enumeration of E. coli in shellfish, provides a considerable saving in time and labor over the standard APHA MPN procedure.</description><subject>Biological and medical sciences</subject><subject>enumeration</subject><subject>Escherichia coli</subject><subject>Fish and seafood industries</subject><subject>fluorimetry</subject><subject>Food industries</subject><subject>food sanitation</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>molluscs</subject><issn>0362-028X</issn><issn>1944-9097</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1987</creationdate><recordtype>article</recordtype><recordid>eNo90D1PHDEQgGELBcFx4Q-kSFykoNnL-HPtMkJAIp2gSJDoLK_XzjraXRP7ViL_Hp_uwM00z4ysF6FPBDacEfENmKQNUPXSCNiojVTiBK2I5rzRoNsPaPUGns7RRSl_AYBqKs_QOQMtBW_JCt3fjkvKafK7HB2uY0g9DiljPy-Tz3YX04xTwDfFDb6SIVrs0hhxnPGUxnEpzs64DH4cQyzDR3Qa7Fj85XGu0ePtze_rH8324e7n9fdt45iWu4YL3bWaOCuEILwXwved6lsmQ1CWC-e977jrRXACaGctQOCScMuC4q1Qmq3R1eHuc07_Fl92ZorF1U_Y2aelGEqhJVIzKSqlB-pyKiX7YJ5znGz-bwiYfUezz2T2mYwAo0ztWJc-H-8v3eT795W3cBV8PQJbC4wh29nF8u4U1aS-yr4cWLDJ2D-5ksdfFAgDwhkwRdkrCrKEqQ</recordid><startdate>19870801</startdate><enddate>19870801</enddate><creator>Rippey, S.R</creator><creator>Chandler, L.A</creator><creator>Watkins, W.D</creator><general>International Association of Milk, Food and Environmental Sanitarians</general><scope>FBQ</scope><scope>IQODW</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>19870801</creationdate><title>Fluorometric method for enumeration of Escherichia coli in molluscan shellfish</title><author>Rippey, S.R ; Chandler, L.A ; Watkins, W.D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c396t-459b791ca55514d55edb8d736ff8a45ceeeb4cd5fc502baa00f4614a3f8475893</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1987</creationdate><topic>Biological and medical sciences</topic><topic>enumeration</topic><topic>Escherichia coli</topic><topic>Fish and seafood industries</topic><topic>fluorimetry</topic><topic>Food industries</topic><topic>food sanitation</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>molluscs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rippey, S.R</creatorcontrib><creatorcontrib>Chandler, L.A</creatorcontrib><creatorcontrib>Watkins, W.D</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of food protection</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rippey, S.R</au><au>Chandler, L.A</au><au>Watkins, W.D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fluorometric method for enumeration of Escherichia coli in molluscan shellfish</atitle><jtitle>Journal of food protection</jtitle><addtitle>J Food Prot</addtitle><date>1987-08-01</date><risdate>1987</risdate><volume>50</volume><issue>8</issue><spage>685</spage><epage>690</epage><pages>685-690</pages><issn>0362-028X</issn><eissn>1944-9097</eissn><coden>JFPRDR</coden><abstract>A novel procedure for enumerating Escherichia coli in molluscan shellfish has been developed and evaluated. The method, a singular modification of the APHA most probable number (MPN) procedure, incorporates a fluorogenic molecule, 4-methylumbelliferyl-β-D-glucuronide (MUG), into the confirmed medium (EC) at a concentration of 50 μg/ml. The substrate could not be incorporated into the presumptive medium (LST) because of fluorescence resulting from the shellfish tissues themselves. After incubation, tubes were examined for fluorescence under long-wave ultraviolet light. Fluorescence indicated presence of E. coli . Of 1151 EC tubes examined for E. coli , both positive and negative for fluorescence, the confirmed positive rate was 91% and the false-negative rate was 11%. Certain problems inherent to the classical MPN procedure itself may understate and overstate these rates, respectively. Of more than 500 E. coli and non- E. coli isolates examined for β-glucuronidase activity, 95% of the E. coli isolates were positive for this enzyme, and only one non- E. coli isolate (a Shigella species) produced the enzyme. The MUG method, which requires only 48 h for enumeration of E. coli in shellfish, provides a considerable saving in time and labor over the standard APHA MPN procedure.</abstract><cop>Des Moines, IA</cop><pub>International Association of Milk, Food and Environmental Sanitarians</pub><pmid>30965471</pmid><doi>10.4315/0362-028x-50.8.685</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0362-028X |
ispartof | Journal of food protection, 1987-08, Vol.50 (8), p.685-690 |
issn | 0362-028X 1944-9097 |
language | eng |
recordid | cdi_proquest_miscellaneous_2207169365 |
source | ScienceDirect Additional Titles |
subjects | Biological and medical sciences enumeration Escherichia coli Fish and seafood industries fluorimetry Food industries food sanitation Fundamental and applied biological sciences. Psychology molluscs |
title | Fluorometric method for enumeration of Escherichia coli in molluscan shellfish |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T23%3A59%3A16IST&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=Fluorometric%20method%20for%20enumeration%20of%20Escherichia%20coli%20in%20molluscan%20shellfish&rft.jtitle=Journal%20of%20food%20protection&rft.au=Rippey,%20S.R&rft.date=1987-08-01&rft.volume=50&rft.issue=8&rft.spage=685&rft.epage=690&rft.pages=685-690&rft.issn=0362-028X&rft.eissn=1944-9097&rft.coden=JFPRDR&rft_id=info:doi/10.4315/0362-028x-50.8.685&rft_dat=%3Cproquest_cross%3E2207169365%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c396t-459b791ca55514d55edb8d736ff8a45ceeeb4cd5fc502baa00f4614a3f8475893%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2207169365&rft_id=info:pmid/30965471&rfr_iscdi=true |