Assumptions of Acceptance Sampling and the Implications for Lot Contamination: Escherichia coli O157 in Lots of Australian Manufacturing Beef

被引:15
作者
Kiermeier, Andreas [1 ]
Mellor, Glen [2 ]
Barlow, Robert [2 ]
Jenson, Ian [3 ]
机构
[1] S Australian Res & Dev Inst, Adelaide, SA 5001, Australia
[2] Commonwealth Sci & Ind Res Org, Div Food & Nutr Sci, Archerfield Bc, Qld 4108, Australia
[3] Meat & Livestock Australia, Sydney, NSW 2059, Australia
关键词
COLI O157-H7; SURVIVAL; SLAUGHTER; PATTIES; CATTLE;
D O I
10.4315/0362-028X.JFP-10-497
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The aims of this work were to determine the distribution and concentration of Escherichia coli 0157 in lots of beef destined for grinding (manufacturing beef) that failed to meet Australian requirements for export, to use these data to better understand the performance of sampling plans based on the binomial distribution, and to consider alternative approaches for evaluating sampling plans. For each of five lots from which E. coli 0157 had been detected, 900 samples from the external carcass surface were tested. E. coli 0157 was not detected in three lots, whereas in two lots E. coli 0157 was detected in 2 and 74 samples. For lots in which E. coli 0157 was not detected in the present study, the E. coli 0157 level was estimated to be <12 cells per 27.2-kg carton. For the most contaminated carton, the total number of E. coli 0157 cells was estimated to be 813. In the two lots in which E. coli 0157 was detected, the pathogen was detected in 1 of 12 and 2 of 12 cartons. The use of acceptance sampling plans based on a binomial distribution can provide a falsely optimistic view of the value of sampling as a control measure when applied to assessment of E. coli 0157 contamination in manufacturing beef. Alternative approaches to understanding sampling plans, which do not assume homogeneous contamination throughout the lot, appear more realistic. These results indicate that despite the application of stringent sampling plans, sampling and testing approaches are inefficient for controlling microbiological quality.
引用
收藏
页码:539 / 544
页数:6
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