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Bayesian inference for quantifying Listeria monocytogenes prevalence and concentration in minced pork meat from presence/absence microbiological testing

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dc.contributor.author Andritsos, ND en
dc.contributor.author Mataragas, M en
dc.contributor.author Paramithiotis, S en
dc.contributor.author Skandamis, PN en
dc.contributor.author Drosinos, EH en
dc.date.accessioned 2014-06-06T06:51:39Z
dc.date.available 2014-06-06T06:51:39Z
dc.date.issued 2012 en
dc.identifier.issn 07400020 en
dc.identifier.uri http://dx.doi.org/10.1016/j.fm.2012.02.016 en
dc.identifier.uri http://62.217.125.90/xmlui/handle/123456789/5617
dc.subject Bayesian inference en
dc.subject Listeria monocytogenes en
dc.subject Pork meat en
dc.subject Presence/absence testing en
dc.subject Prevalence en
dc.subject Uncertainty en
dc.subject.other animal en
dc.subject.other article en
dc.subject.other Bayes theorem en
dc.subject.other food contamination en
dc.subject.other genetics en
dc.subject.other isolation and purification en
dc.subject.other Listeria monocytogenes en
dc.subject.other meat en
dc.subject.other metabolism en
dc.subject.other microbiology en
dc.subject.other statistics en
dc.subject.other swine en
dc.subject.other Animals en
dc.subject.other Bayes Theorem en
dc.subject.other Food Contamination en
dc.subject.other Listeria monocytogenes en
dc.subject.other Meat en
dc.subject.other Swine en
dc.subject.other Listeria monocytogenes en
dc.title Bayesian inference for quantifying Listeria monocytogenes prevalence and concentration in minced pork meat from presence/absence microbiological testing en
heal.type journalArticle en
heal.identifier.primary 10.1016/j.fm.2012.02.016 en
heal.publicationDate 2012 en
heal.abstract The purpose of this work was to estimate the prevalence and concentration of Listeria monocytogenes in minced pork meat by the application of a Bayesian modeling approach. Samples (n = 100) collected from local markets were tested for L. monocytogenes using in parallel the PALCAM, ALOA and RAPID'L. mono selective media. Presence of the pathogen was confirmed through biochemical and molecular tests. Independent experiments (n = 10) for validation purposes were performed. No L. monocytogenes was enumerated by direct-plating (<10 CFU/g), though the pathogen was detected in 22% of the samples. Sensitivity and specificity varied depending on the culture method. L. monocytogenes concentration was estimated at 14-17 CFU/kg. Validation showed good agreement between observed and predicted prevalence (error = -2.17%). The use of at least two culture media in parallel enhanced the efficiency of L. monocytogenes detection. Bayesian modeling may reduce the time needed to draw conclusions regarding L. monocytogenes presence and the uncertainty of the results obtained. © 2012 Elsevier Ltd. en
heal.journalName Food Microbiology en
dc.identifier.issue 2 en
dc.identifier.volume 31 en
dc.identifier.doi 10.1016/j.fm.2012.02.016 en
dc.identifier.spage 148 en
dc.identifier.epage 153 en


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