Real-time PCR methods for the detection of blown pack spoilage causing Clostridium species; C. estertheticum, C. gasigenes and C. ruminantium
dc.contributor.author | Reid, Rachael | |
dc.contributor.author | Burgess, Catherine M. | |
dc.contributor.author | McCabe, Evonne | |
dc.contributor.author | Fanning, Séamus | |
dc.contributor.author | Whyte, Paul | |
dc.contributor.author | Kerry, Joe | |
dc.contributor.author | Bolton, Declan | |
dc.date.accessioned | 2022-12-01T15:43:45Z | |
dc.date.available | 2022-12-01T15:43:45Z | |
dc.date.issued | 2017-11 | |
dc.identifier.citation | Rachael Reid, Catherine M. Burgess, Evonne McCabe, Séamus Fanning, Paul Whyte, Joe Kerry, Declan Bolton, Real-time PCR methods for the detection of blown pack spoilage causing Clostridium species; C. estertheticum, C. gasigenes and C. ruminantium, Meat Science, Volume 133, 2017, Pages 56-60, ISSN 0309-1740, https://doi.org/10.1016/j.meatsci.2017.06.001. | en_US |
dc.identifier.uri | http://hdl.handle.net/11019/2881 | |
dc.description | peer-reviewed | en_US |
dc.description.abstract | A set of real-time PCR methods for the detection of C. estertheticum, C. gasigenes and C. ruminantium, the causative agents of blown pack spoilage (BPS) in vacuum packaged beef, was developed. Robust validation of the sensitivity and specificity was carried out in the three matrices (beef meat drip, wet environmental swabs and dry environmental swabs) as encountered in our testing laboratory and against Clostridium strains (n = 76) and non-Clostridium strains (n = 36). It was possible to detect 4–5 spores per ml for C. estertheticum, 2 spores per ml for C. gasigenes and 8 spores per ml for C. ruminantium, without the need for enrichment of the samples. This high sensitivity is particularly important for the beef sector, not just for testing spoiled product but also in the early detection of contaminated beef and in validation of sporicidal cleaning procedures for critical pieces of equipment such as the vacuum packaging machine, which have the potential to contaminate large volumes of product. | en_US |
dc.description.sponsorship | Food Institutional Research Measure | |
dc.language.iso | en | en_US |
dc.publisher | Elsevier | en_US |
dc.relation.ispartofseries | Meat Science;Vol 133 | |
dc.rights | © 2017 Elsevier Ltd. All rights reserved. | |
dc.rights | Attribution-NonCommercial-ShareAlike 4.0 International | * |
dc.rights.uri | https://www.elsevier.com/tdm/userlicense/1.0/ | |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-sa/4.0/ | * |
dc.subject | Real-time PCR | en_US |
dc.subject | Blown pack spoilage | en_US |
dc.subject | Clostridium estertheticum | en_US |
dc.subject | Clostridium gasigenes | en_US |
dc.subject | Clostridium ruminantium | en_US |
dc.title | Real-time PCR methods for the detection of blown pack spoilage causing Clostridium species; C. estertheticum, C. gasigenes and C. ruminantium | en_US |
dc.type | Article | en_US |
dc.identifier.doi | https://doi.org/10.1016/j.meatsci.2017.06.001 | |
dc.contributor.sponsor | Department of Agriculture, Food and the Marine (Ireland) | en_US |
dc.contributor.sponsor | Teagasc core funding | en_US |
dc.source.volume | 133 | |
dc.source.beginpage | 56 | |
dc.source.endpage | 60 | |
refterms.dateFOA | 2022-12-01T15:43:46Z | |
dc.source.journaltitle | Meat Science |
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