Evaluation of a 24-hour fluorogenic assay for the enumeration of Escherichia coli from foods
A 24 h assay for the detection and enumeration of Escherichia coli in foods was evaluated. The procedure used 4-methylumbelliferyl-beta-D-glucuronide (MUG) incorporated into trypticase soy agar (TSA) and violet red bile agar (VRBA). The procedure was evaluated using 106 different stock cultures, and...
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Veröffentlicht in: | Journal of food protection 1988-10, Vol.51 (10), p.766-769 |
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description | A 24 h assay for the detection and enumeration of Escherichia coli in foods was evaluated. The procedure used 4-methylumbelliferyl-beta-D-glucuronide (MUG) incorporated into trypticase soy agar (TSA) and violet red bile agar (VRBA). The procedure was evaluated using 106 different stock cultures, and 165 isolates from a variety of naturally contaminated foods. Samples were first surface plated on TSA-MUG, and allowed to incubate at room temperature for 1-2 h. Plates were then overlaid with VRBA-MUG and incubated at 35 degrees C for 24 h. The TSA/VRBA-MUG assay was able to detect 94.1% of the E. coli cultures tested, and 95.8% of E. coli strains isolated form foods, giving false-negative rates of 5.9% and 4.2% respectively. False positives were found with 2 of 31 Salmonella spp. isolates and 4 of 4 Shigella spp. isolates from the culture collection. There were no false positives from food isolates. The TSA/VRBA-MUG assay was able to detect E. coli in six food samples that were not detected by our routine procedure. The visible fluorescent halo around each E. coli colony gave immediate confirmation, without the need for further tests. The TSA/VRBA-MUG assay provided an accurate, simple inexpensive method for detection of E. coli, from a wide variety of food products |
doi_str_mv | 10.4315/0362-028X-51.10.766 |
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The procedure used 4-methylumbelliferyl-beta-D-glucuronide (MUG) incorporated into trypticase soy agar (TSA) and violet red bile agar (VRBA). The procedure was evaluated using 106 different stock cultures, and 165 isolates from a variety of naturally contaminated foods. Samples were first surface plated on TSA-MUG, and allowed to incubate at room temperature for 1-2 h. Plates were then overlaid with VRBA-MUG and incubated at 35 degrees C for 24 h. The TSA/VRBA-MUG assay was able to detect 94.1% of the E. coli cultures tested, and 95.8% of E. coli strains isolated form foods, giving false-negative rates of 5.9% and 4.2% respectively. False positives were found with 2 of 31 Salmonella spp. isolates and 4 of 4 Shigella spp. isolates from the culture collection. There were no false positives from food isolates. The TSA/VRBA-MUG assay was able to detect E. coli in six food samples that were not detected by our routine procedure. The visible fluorescent halo around each E. coli colony gave immediate confirmation, without the need for further tests. The TSA/VRBA-MUG assay provided an accurate, simple inexpensive method for detection of E. coli, from a wide variety of food products</description><identifier>ISSN: 0362-028X</identifier><identifier>EISSN: 1944-9097</identifier><identifier>DOI: 10.4315/0362-028X-51.10.766</identifier><identifier>PMID: 28398856</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 ; ESCHERICHIA ; Food industries ; Food microbiology ; Fundamental and applied biological sciences. 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The procedure used 4-methylumbelliferyl-beta-D-glucuronide (MUG) incorporated into trypticase soy agar (TSA) and violet red bile agar (VRBA). The procedure was evaluated using 106 different stock cultures, and 165 isolates from a variety of naturally contaminated foods. Samples were first surface plated on TSA-MUG, and allowed to incubate at room temperature for 1-2 h. Plates were then overlaid with VRBA-MUG and incubated at 35 degrees C for 24 h. The TSA/VRBA-MUG assay was able to detect 94.1% of the E. coli cultures tested, and 95.8% of E. coli strains isolated form foods, giving false-negative rates of 5.9% and 4.2% respectively. False positives were found with 2 of 31 Salmonella spp. isolates and 4 of 4 Shigella spp. isolates from the culture collection. There were no false positives from food isolates. The TSA/VRBA-MUG assay was able to detect E. coli in six food samples that were not detected by our routine procedure. The visible fluorescent halo around each E. coli colony gave immediate confirmation, without the need for further tests. The TSA/VRBA-MUG assay provided an accurate, simple inexpensive method for detection of E. coli, from a wide variety of food products</description><subject>Biological and medical sciences</subject><subject>ESCHERICHIA</subject><subject>Food industries</subject><subject>Food microbiology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>HIDROLASAS</subject><subject>HIGIENE DE LOS ALIMENTOS</subject><subject>HYDROLASE</subject><subject>HYGIENE DES ALIMENTS</subject><subject>TECHNIQUE DE CULTURE</subject><subject>TECNICAS DE CULTIVO</subject><issn>0362-028X</issn><issn>1944-9097</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1988</creationdate><recordtype>article</recordtype><recordid>eNo90MtKAzEUBuAgiq3VF1CQLFy4mZr7ZSmlXqDgQgsuhJBmknZkZlKTjtC3d0prVwcO338O_ADcYDRmFPMHRAUpEFGfBcfjfimFOAFDrBkrNNLyFAyPYgAucv5GCBFNxDkYEEW1UlwMwdf019ad3VSxhTFACwkrVrFLMNRdTHHp28pBm7PdwhAT3Kw89G3X-HSMTLNb-VS5VWWhi3UFQ4pNj2OZL8FZsHX2V4c5AvOn6cfkpZi9Pb9OHmeFo0RtCoU5U5IiJIPkSGmqiMAEeyE1DY46V3LCF4tSOxwQ89ySRSh5qYgWXFrF6Ajc7--uU_zpfN6YpsrO17VtfeyywUpJxLHGuKd0T12KOScfzDpVjU1bg5HZ1Wp2pZldaYbj3bKvtU_dHh50i8aXx8x_jz24OwCbna1Dsq2r8tFJxRlipGfXexZsNHaZejJ_V0pIyjD9A-pthuI</recordid><startdate>19881001</startdate><enddate>19881001</enddate><creator>Weiss, L.H</creator><creator>Humber, J</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>19881001</creationdate><title>Evaluation of a 24-hour fluorogenic assay for the enumeration of Escherichia coli from foods</title><author>Weiss, L.H ; Humber, J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c328t-8154873007f750893826121e6793fc3ccd525bbd9c1f04e5a2bfd5d829657a843</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1988</creationdate><topic>Biological and medical sciences</topic><topic>ESCHERICHIA</topic><topic>Food industries</topic><topic>Food microbiology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>HIDROLASAS</topic><topic>HIGIENE DE LOS ALIMENTOS</topic><topic>HYDROLASE</topic><topic>HYGIENE DES ALIMENTS</topic><topic>TECHNIQUE DE CULTURE</topic><topic>TECNICAS DE CULTIVO</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Weiss, L.H</creatorcontrib><creatorcontrib>Humber, J</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>Weiss, L.H</au><au>Humber, J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of a 24-hour fluorogenic assay for the enumeration of Escherichia coli from foods</atitle><jtitle>Journal of food protection</jtitle><addtitle>J Food Prot</addtitle><date>1988-10-01</date><risdate>1988</risdate><volume>51</volume><issue>10</issue><spage>766</spage><epage>769</epage><pages>766-769</pages><issn>0362-028X</issn><eissn>1944-9097</eissn><coden>JFPRDR</coden><abstract>A 24 h assay for the detection and enumeration of Escherichia coli in foods was evaluated. The procedure used 4-methylumbelliferyl-beta-D-glucuronide (MUG) incorporated into trypticase soy agar (TSA) and violet red bile agar (VRBA). The procedure was evaluated using 106 different stock cultures, and 165 isolates from a variety of naturally contaminated foods. Samples were first surface plated on TSA-MUG, and allowed to incubate at room temperature for 1-2 h. Plates were then overlaid with VRBA-MUG and incubated at 35 degrees C for 24 h. The TSA/VRBA-MUG assay was able to detect 94.1% of the E. coli cultures tested, and 95.8% of E. coli strains isolated form foods, giving false-negative rates of 5.9% and 4.2% respectively. False positives were found with 2 of 31 Salmonella spp. isolates and 4 of 4 Shigella spp. isolates from the culture collection. There were no false positives from food isolates. The TSA/VRBA-MUG assay was able to detect E. coli in six food samples that were not detected by our routine procedure. The visible fluorescent halo around each E. coli colony gave immediate confirmation, without the need for further tests. The TSA/VRBA-MUG assay provided an accurate, simple inexpensive method for detection of E. coli, from a wide variety of food products</abstract><cop>Des Moines, IA</cop><pub>International Association of Milk, Food and Environmental Sanitarians</pub><pmid>28398856</pmid><doi>10.4315/0362-028X-51.10.766</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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source | Free E-Journal (出版社公開部分のみ); ProQuest Central UK/Ireland; Alma/SFX Local Collection |
subjects | Biological and medical sciences ESCHERICHIA Food industries Food microbiology Fundamental and applied biological sciences. Psychology HIDROLASAS HIGIENE DE LOS ALIMENTOS HYDROLASE HYGIENE DES ALIMENTS TECHNIQUE DE CULTURE TECNICAS DE CULTIVO |
title | Evaluation of a 24-hour fluorogenic assay for the enumeration of Escherichia coli from foods |
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