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<article article-type="research-article" dtd-version="2.3" xml:lang="EN" annotation-version="1.0"><front><journal-meta><journal-id journal-id-type="hwp">mmb</journal-id><journal-id journal-id-type="publisher-id">mmb</journal-id><journal-title>Meat and Muscle Biology</journal-title><abbrev-journal-title abbrev-type="full">MMB</abbrev-journal-title><issn pub-type="epub">2575-985X</issn><publisher><publisher-name>American Meat Science Association</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">rmc2016.112</article-id><article-id pub-id-type="doi">10.221751/rmc2016.112</article-id><article-categories><subj-group subj-group-type="heading"><subject>2016 Reciprocal Meat Conference – Meat and Poultry Safety</subject></subj-group></article-categories><title-group><article-title>Thermal Inactivation of Salmonella and Listeria Monocytogenes in Beef Patties, Chicken Patties, Chicken Tenders, and High-Fat Frankfurters</article-title></title-group><contrib-group><contrib contrib-type="author" corresp="yes" contact-id="0" contact-type="auto"><name><surname>Mcminn</surname><given-names>R. P.</given-names></name><aff><label>1</label>University of Wisconsin-Madison, Madison, WI, USA</aff></contrib><contrib contrib-type="author" contact-id="0" contact-type="auto"><name><surname>Sindelar</surname><given-names>J. J.</given-names></name><aff><label>1</label>University of Wisconsin-Madison, Madison, WI, USA</aff></contrib><contrib contrib-type="author" contact-id="0" contact-type="auto"><name><surname>Glass</surname><given-names>K.</given-names></name><aff><label>1</label>University of Wisconsin-Madison, Madison, WI, USA</aff></contrib><contrib contrib-type="author" contact-id="0" contact-type="auto"><name><surname>Hanson</surname><given-names>R.</given-names></name><aff><label>2</label>HansonTech, Hudson, WI, USA</aff></contrib></contrib-group><pub-date pub-type="ppub"><month>09</month><year>2018</year></pub-date><volume>1</volume><issue>2</issue><fpage>115</fpage><lpage>115</lpage><permissions><copyright-year>2018</copyright-year><copyright-holder>American Meat Science Association</copyright-holder><license license-type="open-access"><p>This is an open access article distributed under the CC BY-NC-ND license (<ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by-nc-nd/4.0/" xmlns:xlink="http://www.w3.org/1999/xlink">http://creativecommons.org/licenses/by-nc-nd/4.0/</ext-link>)</p></license></permissions><abstract><sec><title>Objectives</title><p>To determine the temperature-death times of <italic>Salmonella</italic> and <italic>L. monocytogenes</italic> in beef patties, chicken patties, chicken tenders, and frankfurter batter at four different temperatures and validate these findings using commercial products and cooking processes.</p></sec><sec><title>Materials and Methods</title><p><bold><italic>D-value determination.</italic></bold> Two hundred grams of finely ground meat were inoculated to 8-log cfu/g of either <italic>Salmonella</italic> or <italic>L. monocytogenes</italic> (5-strain mixtures). One-g samples of inoculated meat were flattened into a thin film in moisture-impermeable pouches and vacuum-packaged. Samples were heated at one of four temperatures (54.4, 60.0, 65.6, and 71.1°C) in a water bath. Triplicate samples were removed periodically during cooking, chilled to ≤ 4°C, and enumerated for the survival of <italic>Salmonella</italic> or <italic>L. monocytogenes</italic>. D-values were calculated from the linear regression on log reduction of pathogen versus time. This experiment was replicated three times.</p><p><bold><italic>Batch oven validation.</italic></bold> Inoculated frankfurter links were thermally processed in a combination steam/convection oven following one of 2 cook schedules until an internal temperature of 71.1°C was achieved. The control cycle met USDA, FSIS Appendix A relative humidity requirements while the test cycle only applied steam during the final step of the process. For both cycles, triplicate links were removed when product internal temperature reached 54.4°C, 62.7°C, and 71.1°C. This experiment was replicated twice.</p><p><bold><italic>Impingement oven validation.</italic></bold> Inoculated beef patties, chicken patties and, chicken tenders were cooked via passage through two in-line impingement ovens. Samples were cooked to one of two temperatures (71.1°C and 79.4°C for poultry, 71.1°C and 76.7°C for beef) following either a control cycle or a test cycle. The control cycle applied no steam while the test cycle used a target wet-bulb temperature of 71.1°C (for target 1.2% rH) in the second oven. For each trial, triplicate samples were removed prior to cooking and on exit from each oven for enumeration of surviving pathogens. This experiment was replicated twice<underline>.</underline></p></sec><sec><title>Results</title><p>D-values for <italic>Salmonella</italic> were shorter than those for <italic>L. monocytogenes</italic> across all products and temperatures tested. For batch oven cooking, both cook cycles resulted in ≥ 5.0 log reduction of <italic>Salmonella</italic> and <italic>L. monocytogenes</italic> in frankfurters. With a target temperature of 71.1°C, the control and tests cycles produced a 4.21 ± 2.22 and 5.53 ± 0.06 log reduction of <italic>L. monocytogenes</italic> in chicken tenders, respectively, during impingement cooking. Neither cycle was able to produce ≥ 5.0 log reduction of <italic>Salmonella</italic> in chicken tenders cooked to 71.1°C.</p></sec><sec><title>Conclusion</title><p>For non-impingement processes USDA, FSIS Appendix A time-temperature recommendations are adequate for controlling 1) <italic>Salmonella</italic> when the final cooking temperature meets or exceeds 60.0°C and 2) <italic>L. monocytogenes</italic> when the final cooking temperature meets or exceeds 71.1°C. <italic>Salmonella</italic> is more thermotolerant than <italic>L. monocytogenes</italic> during impingement processing. D-values suggested that 71.1°C should produce an instantaneous ≥ 5.0 log reduction of <italic>Salmonella</italic> however this was not observed in rapid processes ( ≤ 4.0 min) Incorporation of high wet-bulb temperature targets into impingement processes may be necessary to ensure adequate control of <italic>Salmonella.</italic></p></sec></abstract><kwd-group><title>Keywords: </title><kwd>Impingement Oven</kwd><kwd>Salmonella</kwd><kwd>Listeria</kwd><kwd>Thermal Inactivation</kwd><kwd>Thermal Processing</kwd><kwd>USDA</kwd><kwd>FSIS Appendix A</kwd></kwd-group></article-meta><custom-meta-wrap><custom-meta><meta-name>author</meta-name><meta-value>Mcminn R. P.</meta-value></custom-meta><custom-meta><meta-name>author</meta-name><meta-value>Sindelar J. J.</meta-value></custom-meta><custom-meta><meta-name>author</meta-name><meta-value>Glass K.</meta-value></custom-meta><custom-meta><meta-name>author</meta-name><meta-value>Hanson R.</meta-value></custom-meta></custom-meta-wrap><ar:concepts xmlns:ar="http://appliedrelevance.com"/></front><custom-meta-container><journal-date-data><jdate>2018-09-13</jdate></journal-date-data><journal-year>2018</journal-year><journal-month>09</journal-month><journal-title>Meat and Muscle Biology</journal-title><journal-issue>2</journal-issue><journal-fpage>115</journal-fpage><journal-volume>1</journal-volume><journal-lpage>115</journal-lpage><insert-date>September 13, 2018</insert-date></custom-meta-container></article>
