Validation of a traditional Italian-style salami manufacturing process for control of salmonella and Listeria monocytogenes
dc.citation.epage | 800 | en_US |
dc.citation.issn | 0362-028X | en_US |
dc.citation.issue | 4 | en_US |
dc.citation.jtitle | Journal of food protection | en_US |
dc.citation.spage | 794 | en_US |
dc.citation.volume | 69 | en_US |
dc.contributor.author | Nightingale, K.K. | en_US |
dc.contributor.author | Thippareddi, H. | en_US |
dc.contributor.author | Phebus, Randall K. | en_US |
dc.contributor.author | Marsden, James L. | en_US |
dc.contributor.author | Nutsch, Abbey L. | en_US |
dc.contributor.authoreid | phebus | |
dc.contributor.authoreid | jmarsden | |
dc.contributor.authoreid | anutsch | |
dc.date.accessioned | 2008-03-28T01:45:53Z | |
dc.date.available | 2008-03-28T01:45:53Z | |
dc.date.issued | 2008-03-28T01:45:53Z | |
dc.date.published | 2006 | en_US |
dc.description.abstract | Italian-style salami batter (formulated with pork shoulder) was inoculated with ca. 7.0 log CFU/g of either Salmonella or Listeria monocytogenes. Salami links (55-mm cellulose casings) were fermented at 308C for 24, 40, or 72 h and then dried to target moisture/protein ratios (MPRs) of 1.9:1 or 1.4:1. Links were sampled after fermentation (24, 40, and 72 h) and after combined fermentation-drying treatments (MPRs of 1.9:1 and 1.4:1 for all fermentation periods), and microbiological and proximate analyses were performed at each sampling. Pathogen populations were enumerated by direct plating on selective agar and by an injured-cell recovery method. When enumerated by the injured-cell recovery method, Salmonella populations were reduced by 1.2 to 2.1 log CFU/g after fermentation alone (24 to 72 h) and by 2.4 to 3.4 log CFU/g when fermentation was followed by drying. Drying to an MPR of 1.4:1 was no more effective than drying to an MPR of 1.9:1 (P . 0.05). When enumerated directly on selective media, Salmonella populations were reduced from 1.6 to 2.4 log CFU/g and from 3.6 to 4.5 log CFU/g for fermentation alone and fermentation followed by drying, respectively. L. monocytogenes populations were reduced by ,1.0 log CFU/g following all fermentation and combined fermentation-drying treatments, regardless of the enumeration method. These results suggest that the Italian-style salami manufacturing process evaluated does not adequately reduce high pathogen loads. Processors may thus need to consider supplemental measures, such as raw material specifications and a final heating step, to enhance the lethality of the overall manufacturing process. | en_US |
dc.identifier.uri | http://hdl.handle.net/2097/584 | |
dc.rights | Reprinted with permission from the Journal of food protection. Copyright held by the International Association for Food Protection, Des Moines, Iowa, U.S.A. | en_US |
dc.subject | Validation | en_US |
dc.subject | Salami | en_US |
dc.subject | Salmonella | en_US |
dc.subject | Listeria monocytogenes | en_US |
dc.subject | Fermentation | en_US |
dc.subject | Processed meats | en_US |
dc.title | Validation of a traditional Italian-style salami manufacturing process for control of salmonella and Listeria monocytogenes | en_US |
dc.type | Article (publisher version) | en_US |