Comparison of recovery methods for freeze-injured Listeria monocytogenes, Salmonella Typhimurium, and Campylobacter coli in cell suspensions and associated with pork surfaces
Cells injured as a result of freezing, heating, and acidification treatments may not grow during conventional microbiological procedures owing to the presence of selective agents, compounds, or dyes in the media, impairing the cell's ability to repair itself and grow. Injured cells can be recov...
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description | Cells injured as a result of freezing, heating, and acidification treatments may not grow during conventional microbiological procedures owing to the presence of selective agents, compounds, or dyes in the media, impairing the cell's ability to repair itself and grow. Injured cells can be recovered by combining selective and nonselective media into a single system. With such combinations, the diffusion of the selective compounds or dyes is controlled, allowing for the resuscitation of injured cells of interest while also inhibiting the growth of undesirable background microflora. In this study, Listeria monocytogenes, Salmonella Typhimurium, and Campylobacter coli suspended in buffer or associated with pork surfaces were subjected to a freeze-thaw cycle (-15 degrees C for 24 h, 4 degrees C for 4 h). Following treatments, freeze-injured cells were plated on appropriate media for the overlay (OV), thin agar layer (TAL), and Lutri plate (LP) recovery methods. The levels of L. monocytogenes and Salmonella Typhimurium recovered from cell suspensions and pork surfaces by the TAL, OV, and LP methods following freeze treatments were not statistically different (P > 0.05) from recovery levels associated with nonselective media. Conversely, levels of pathogens on selective media were significantly reduced compared with those for the other methods employed. The TAL method's recovery of C. coli was not significantly different from that achieved with the nonselective media. Overall, the results presented in this study demonstrate that the TAL method not only was easier to perform, but also allowed improved isolation of single colonies for further characterization. This study may provide researchers with better methods to determine the effectiveness of industry-employed chilling processes in reducing pathogenic bacteria associated with red meat surfaces. |
doi_str_mv | 10.4315/0362-028X-66.5.798 |
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Injured cells can be recovered by combining selective and nonselective media into a single system. With such combinations, the diffusion of the selective compounds or dyes is controlled, allowing for the resuscitation of injured cells of interest while also inhibiting the growth of undesirable background microflora. In this study, Listeria monocytogenes, Salmonella Typhimurium, and Campylobacter coli suspended in buffer or associated with pork surfaces were subjected to a freeze-thaw cycle (-15 degrees C for 24 h, 4 degrees C for 4 h). Following treatments, freeze-injured cells were plated on appropriate media for the overlay (OV), thin agar layer (TAL), and Lutri plate (LP) recovery methods. The levels of L. monocytogenes and Salmonella Typhimurium recovered from cell suspensions and pork surfaces by the TAL, OV, and LP methods following freeze treatments were not statistically different (P > 0.05) from recovery levels associated with nonselective media. Conversely, levels of pathogens on selective media were significantly reduced compared with those for the other methods employed. The TAL method's recovery of C. coli was not significantly different from that achieved with the nonselective media. Overall, the results presented in this study demonstrate that the TAL method not only was easier to perform, but also allowed improved isolation of single colonies for further characterization. This study may provide researchers with better methods to determine the effectiveness of industry-employed chilling processes in reducing pathogenic bacteria associated with red meat surfaces.</description><identifier>ISSN: 0362-028X</identifier><identifier>EISSN: 1944-9097</identifier><identifier>DOI: 10.4315/0362-028X-66.5.798</identifier><identifier>PMID: 12747688</identifier><identifier>CODEN: JFPRDR</identifier><language>eng</language><publisher>Des Moines, IA: International Association of Milk, Food and Environmental Sanitarians</publisher><subject><![CDATA[Agar ; Animals ; bacterial contamination ; Bacteriological Techniques ; Biological and medical sciences ; Campylobacter coli ; Campylobacter coli - growth & development ; Campylobacter coli - isolation & purification ; cold injury ; Colony Count, Microbial ; Culture Media ; food contamination ; Food industries ; Food Microbiology ; food pathogens ; freeze-injured bacteria ; Freezing ; Fundamental and applied biological sciences. Psychology ; laboratory techniques ; Listeria monocytogenes ; Listeria monocytogenes - growth & development ; Listeria monocytogenes - isolation & purification ; lutri plate method ; Meat - microbiology ; Meat and meat product industries ; microbial resuscitation ; overlay method ; pork ; Salmonella typhimurium ; Salmonella typhimurium - growth & development ; Salmonella typhimurium - isolation & purification ; stress tolerance ; surface area ; Swine ; thin agar layer method]]></subject><ispartof>Journal of food protection, 2003-05, Vol.66 (5), p.798-803</ispartof><rights>2003 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c428t-dd0f7d1d777deba70118cccb21f76ded1ff5134417b9277d91a8f9e2315227343</citedby><cites>FETCH-LOGICAL-c428t-dd0f7d1d777deba70118cccb21f76ded1ff5134417b9277d91a8f9e2315227343</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27929,27930</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14805390$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12747688$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chang, V.P</creatorcontrib><creatorcontrib>Mills, E.W</creatorcontrib><creatorcontrib>Cutter, C.N</creatorcontrib><title>Comparison of recovery methods for freeze-injured Listeria monocytogenes, Salmonella Typhimurium, and Campylobacter coli in cell suspensions and associated with pork surfaces</title><title>Journal of food protection</title><addtitle>J Food Prot</addtitle><description>Cells injured as a result of freezing, heating, and acidification treatments may not grow during conventional microbiological procedures owing to the presence of selective agents, compounds, or dyes in the media, impairing the cell's ability to repair itself and grow. Injured cells can be recovered by combining selective and nonselective media into a single system. With such combinations, the diffusion of the selective compounds or dyes is controlled, allowing for the resuscitation of injured cells of interest while also inhibiting the growth of undesirable background microflora. In this study, Listeria monocytogenes, Salmonella Typhimurium, and Campylobacter coli suspended in buffer or associated with pork surfaces were subjected to a freeze-thaw cycle (-15 degrees C for 24 h, 4 degrees C for 4 h). Following treatments, freeze-injured cells were plated on appropriate media for the overlay (OV), thin agar layer (TAL), and Lutri plate (LP) recovery methods. The levels of L. monocytogenes and Salmonella Typhimurium recovered from cell suspensions and pork surfaces by the TAL, OV, and LP methods following freeze treatments were not statistically different (P > 0.05) from recovery levels associated with nonselective media. Conversely, levels of pathogens on selective media were significantly reduced compared with those for the other methods employed. The TAL method's recovery of C. coli was not significantly different from that achieved with the nonselective media. Overall, the results presented in this study demonstrate that the TAL method not only was easier to perform, but also allowed improved isolation of single colonies for further characterization. This study may provide researchers with better methods to determine the effectiveness of industry-employed chilling processes in reducing pathogenic bacteria associated with red meat surfaces.</description><subject>Agar</subject><subject>Animals</subject><subject>bacterial contamination</subject><subject>Bacteriological Techniques</subject><subject>Biological and medical sciences</subject><subject>Campylobacter coli</subject><subject>Campylobacter coli - growth & development</subject><subject>Campylobacter coli - isolation & purification</subject><subject>cold injury</subject><subject>Colony Count, Microbial</subject><subject>Culture Media</subject><subject>food contamination</subject><subject>Food industries</subject><subject>Food Microbiology</subject><subject>food pathogens</subject><subject>freeze-injured bacteria</subject><subject>Freezing</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>laboratory techniques</subject><subject>Listeria monocytogenes</subject><subject>Listeria monocytogenes - growth & development</subject><subject>Listeria monocytogenes - isolation & purification</subject><subject>lutri plate method</subject><subject>Meat - microbiology</subject><subject>Meat and meat product industries</subject><subject>microbial resuscitation</subject><subject>overlay method</subject><subject>pork</subject><subject>Salmonella typhimurium</subject><subject>Salmonella typhimurium - growth & development</subject><subject>Salmonella typhimurium - isolation & purification</subject><subject>stress tolerance</subject><subject>surface area</subject><subject>Swine</subject><subject>thin agar layer method</subject><issn>0362-028X</issn><issn>1944-9097</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpF0k-P1CAYBvDGaNxx9Qt4UC562o5AaWmPZuK_ZBIPu5t4IxRedlhbqLytpn4oP6OMM3FPJOT3vBAeiuIlo1tRsfodrRpeUt5-K5tmW29l1z4qNqwTouxoJx8Xm__goniGeE8p5R1vnhYXjEshm7bdFH92cZx08hgDiY4kMPEnpJWMMB-iReJiIi4B_IbSh_slgSV7jzMkr8kYQzTrHO8gAF6Raz3kHRgGTW7W6eDHJfllvCI6WLLT47QOsdcmR4mJgyc-EJMxwQUnCOhjwH9UI0bj9ZxP-uXnA5li-p5RctoAPi-eOD0gvDivl8Xtxw83u8_l_uunL7v3-9II3s6ltdRJy6yU0kKvJWWsNcb0nDnZWLDMuZpVQjDZdzybjunWdcDzq3IuK1FdFm9Pc6cUfyyAsxo9Hq-rA8QFFWu7SnLRZshP0KSImMCpKflRp1Uxqo4tqWMJ6liCahpVq9xSDr06T1_6EexD5FxLBm_OQKPRg0s6GI8PTrS0rjqa3euTczoqfZdrVLfXnLKKsvwDOG-qv40EqMs</recordid><startdate>20030501</startdate><enddate>20030501</enddate><creator>Chang, V.P</creator><creator>Mills, E.W</creator><creator>Cutter, C.N</creator><general>International Association of Milk, Food and Environmental Sanitarians</general><scope>FBQ</scope><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>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>20030501</creationdate><title>Comparison of recovery methods for freeze-injured Listeria monocytogenes, Salmonella Typhimurium, and Campylobacter coli in cell suspensions and associated with pork surfaces</title><author>Chang, V.P ; Mills, E.W ; Cutter, C.N</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c428t-dd0f7d1d777deba70118cccb21f76ded1ff5134417b9277d91a8f9e2315227343</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Agar</topic><topic>Animals</topic><topic>bacterial contamination</topic><topic>Bacteriological Techniques</topic><topic>Biological and medical sciences</topic><topic>Campylobacter coli</topic><topic>Campylobacter coli - growth & development</topic><topic>Campylobacter coli - isolation & purification</topic><topic>cold injury</topic><topic>Colony Count, Microbial</topic><topic>Culture Media</topic><topic>food contamination</topic><topic>Food industries</topic><topic>Food Microbiology</topic><topic>food pathogens</topic><topic>freeze-injured bacteria</topic><topic>Freezing</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>laboratory techniques</topic><topic>Listeria monocytogenes</topic><topic>Listeria monocytogenes - growth & development</topic><topic>Listeria monocytogenes - isolation & purification</topic><topic>lutri plate method</topic><topic>Meat - microbiology</topic><topic>Meat and meat product industries</topic><topic>microbial resuscitation</topic><topic>overlay method</topic><topic>pork</topic><topic>Salmonella typhimurium</topic><topic>Salmonella typhimurium - growth & development</topic><topic>Salmonella typhimurium - isolation & purification</topic><topic>stress tolerance</topic><topic>surface area</topic><topic>Swine</topic><topic>thin agar layer method</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chang, V.P</creatorcontrib><creatorcontrib>Mills, E.W</creatorcontrib><creatorcontrib>Cutter, C.N</creatorcontrib><collection>AGRIS</collection><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>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Journal of food protection</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chang, V.P</au><au>Mills, E.W</au><au>Cutter, C.N</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparison of recovery methods for freeze-injured Listeria monocytogenes, Salmonella Typhimurium, and Campylobacter coli in cell suspensions and associated with pork surfaces</atitle><jtitle>Journal of food protection</jtitle><addtitle>J Food Prot</addtitle><date>2003-05-01</date><risdate>2003</risdate><volume>66</volume><issue>5</issue><spage>798</spage><epage>803</epage><pages>798-803</pages><issn>0362-028X</issn><eissn>1944-9097</eissn><coden>JFPRDR</coden><abstract>Cells injured as a result of freezing, heating, and acidification treatments may not grow during conventional microbiological procedures owing to the presence of selective agents, compounds, or dyes in the media, impairing the cell's ability to repair itself and grow. Injured cells can be recovered by combining selective and nonselective media into a single system. With such combinations, the diffusion of the selective compounds or dyes is controlled, allowing for the resuscitation of injured cells of interest while also inhibiting the growth of undesirable background microflora. In this study, Listeria monocytogenes, Salmonella Typhimurium, and Campylobacter coli suspended in buffer or associated with pork surfaces were subjected to a freeze-thaw cycle (-15 degrees C for 24 h, 4 degrees C for 4 h). Following treatments, freeze-injured cells were plated on appropriate media for the overlay (OV), thin agar layer (TAL), and Lutri plate (LP) recovery methods. The levels of L. monocytogenes and Salmonella Typhimurium recovered from cell suspensions and pork surfaces by the TAL, OV, and LP methods following freeze treatments were not statistically different (P > 0.05) from recovery levels associated with nonselective media. Conversely, levels of pathogens on selective media were significantly reduced compared with those for the other methods employed. The TAL method's recovery of C. coli was not significantly different from that achieved with the nonselective media. Overall, the results presented in this study demonstrate that the TAL method not only was easier to perform, but also allowed improved isolation of single colonies for further characterization. This study may provide researchers with better methods to determine the effectiveness of industry-employed chilling processes in reducing pathogenic bacteria associated with red meat surfaces.</abstract><cop>Des Moines, IA</cop><pub>International Association of Milk, Food and Environmental Sanitarians</pub><pmid>12747688</pmid><doi>10.4315/0362-028X-66.5.798</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Agar Animals bacterial contamination Bacteriological Techniques Biological and medical sciences Campylobacter coli Campylobacter coli - growth & development Campylobacter coli - isolation & purification cold injury Colony Count, Microbial Culture Media food contamination Food industries Food Microbiology food pathogens freeze-injured bacteria Freezing Fundamental and applied biological sciences. Psychology laboratory techniques Listeria monocytogenes Listeria monocytogenes - growth & development Listeria monocytogenes - isolation & purification lutri plate method Meat - microbiology Meat and meat product industries microbial resuscitation overlay method pork Salmonella typhimurium Salmonella typhimurium - growth & development Salmonella typhimurium - isolation & purification stress tolerance surface area Swine thin agar layer method |
title | Comparison of recovery methods for freeze-injured Listeria monocytogenes, Salmonella Typhimurium, and Campylobacter coli in cell suspensions and associated with pork surfaces |
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