RAPID REAL-TIME PCR ASSAY FOR DETECTING SALMONELLA IN RAW AND READY-TO-EAT MEATS

被引:8
作者
Patel, Jitu R. [1 ]
Bhagwat, Arvind A. [2 ]
机构
[1] Agr Res Serv, Produce Qual & Safety Lab, USDA, Beltsville, MD 20705 USA
[2] Agr Res Serv, Food Safety Lab, USDA, Beltsville, MD 20705 USA
关键词
Salmonella; real-time PCR; chicken; pork; ready-to-eat meats; molecular beacon;
D O I
10.1556/AVet.56.2008.4.3
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
A real-time PCR assay was evaluated for the rapid detection (10 h) of Salmonella in meats using molecular beacon probes available as a commercial kit (iQ-Check, Bio-Rad laboratories). Raw (chicken, pork) and ready-to-eat (RTE) meats were artificially contaminated with Salmonella enterica serovar Typhimurium at the estimated level of 2 to 4 cells per 25 g. After 8 h of pre-enrichment in buffered peptone water, a molecular beacon-based PCR assay was performed to detect contamination in raw and RTE meats. The sensitivity and accuracy of the assay were compared with the conventional USDA microbiological procedure. Comparative evaluation of the USDA procedure with the rapid PCR assay for meat samples (n = 63) revealed 1 false negative pork sample with the PCR assay. All uninoculated controls (n = 34) but one sample were negative by both the 10-h PCR assay and the USDA procedure. Developing rapid pathogen detection methods with shorter pre-enrichment times (8-h) and real-time data monitoring capabilities will benefit the industry in preventing recall of contaminated meats by stopping the contaminated products from being introduced into the marketplace.
引用
收藏
页码:451 / 458
页数:8
相关论文
共 21 条
  • [1] Simultaneous detection of Escherichia coli O157:H7, Listeria monocytogenes and Salmonella strains by real-time PCR
    Bhagwat, AA
    [J]. INTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY, 2003, 84 (02) : 217 - 224
  • [2] The evaluation of a fluorogenic polymerase chain reaction assay for the detection of Salmonella species in food commodities
    Chen, S
    Yee, A
    Griffiths, M
    Larkin, C
    Yamashiro, CT
    Behari, R
    PaszkoKolva, C
    Rahn, K
    DeGrandis, SA
    [J]. INTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY, 1997, 35 (03) : 239 - 250
  • [3] ERS, 2001, EC FOODB DIS EST BEN
  • [4] Fung DYC, 2002, J AOAC INT, V85, P1000
  • [5] Optimization of a 12-hour TaqMan PCR-based method for detection of Salmonella bacteria in meat
    Josefsen, M. H.
    Krause, M.
    Hansen, F.
    Hoorfar, J.
    [J]. APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2007, 73 (09) : 3040 - 3048
  • [6] Multiplex PCR for simultaneous detection of Salmonella spp., Listeria monocytogenes, and Escherichia coli O157:H7 in meat samples
    Kawasaki, S
    Horikoshi, N
    Okada, Y
    Takeshita, K
    Sameshima, T
    Kawamoto, S
    [J]. JOURNAL OF FOOD PROTECTION, 2005, 68 (03) : 551 - 556
  • [7] Application of a molecular beacon -: real-time PCR technology to detect Salmonella species contaminating fruits and vegetables
    Liming, SH
    Bhagwat, AA
    [J]. INTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY, 2004, 95 (02) : 177 - 187
  • [8] An improved PCR primer pair based on 16S rDNA for the specific detection of Salmonella serovars in food samples
    Lin, CK
    Hung, CL
    Hsu, SC
    Tsai, CC
    Tsen, HY
    [J]. JOURNAL OF FOOD PROTECTION, 2004, 67 (07) : 1335 - 1343
  • [9] NUCLEOTIDE-SEQUENCE OF IAGA AND IAGB GENES INVOLVED IN INVASION OF HELA-CELLS BY SALMONELLA-ENTERICA SUBSP ENTERICA SER TYPHI
    MIRAS, I
    HERMANT, D
    ARRICAU, N
    POPOFF, MY
    [J]. RESEARCH IN MICROBIOLOGY, 1995, 146 (01) : 17 - 20
  • [10] Evaluation of an immunomagnetic separation-real-time PCR assay for the rapid detection of Salmonella in meat
    Notzon, Angelika
    Helmuth, Reiner
    Bauer, Johann
    [J]. JOURNAL OF FOOD PROTECTION, 2006, 69 (12) : 2896 - 2901