Comparative Evaluation of RTi-PCR and Mini-VIDAS SLM System as Predictive Tools for the Routine Detection of Salmonella spp. in Naturally Contaminated Food Products

被引:7
作者
Elizaquivel, P. [1 ]
Gabaldon, J. A. [3 ]
Aznar, R. [1 ,2 ]
机构
[1] Univ Valencia, Dept Microbiol & Ecol, E-46100 Valencia, Spain
[2] Univ Valencia, Dept Biotechnol, Inst Agroquim & Tecnol Alimentos, Consejo Super Invest Cient, E-46100 Valencia, Spain
[3] Ctr Tecnol Nacl Conserva & Alimentac, Dept Seguridad Alimentaria, Murcia, Spain
关键词
Salmonella spp; Mini-VIDAS SLM; PCR; RTi-PCR; Food; REAL-TIME PCR; RAPID DETECTION; IMMUNOMAGNETIC SEPARATION; COMBINATION; CULTURE; WATER; ELISA; ASSAY; DNA;
D O I
10.1007/s12161-008-9042-3
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
In the present work, we have evaluated a real-time polymerase chain reaction-based method (RTi-PCR) as a routine laboratory test, by comparing the results obtained in two laboratories with the mini-VIDAS SLM (bioM,rieux), a standard accepted immunoenzymatic (enzyme-linked immunosorbent assay) method currently used in the food industry. To that aim, a set of 141 naturally contaminated food samples were analyzed after an enrichment step by conventional PCR and mini-VIDAS and prior to the enrichment by RTi-PCR. Results from both laboratories were statistically analyzed using the kappa coefficients, which indicated a perfect agreement between them. Out of the 141 samples, 11 were positive for Salmonella detection by mini-VIDAS, 35 by conventional PCR in Lab1, and 44 in Lab2. Twenty-eight of them tested positive by RTi-PCR in Lab1 and 31 in Lab2. In order to use the evaluated methods as a diagnostic test, their predictive capacity was analyzed on the basis of their positive and negative predictive values, calculated using the result obtained-after enrichment-by conventional PCR as the "gold standard." Both positive and negative predictive values were higher for RTi-PCR than those obtained for mini-VIDAS, indicating good performance of the RTi-PCR technique-applied without enrichment-in the detection of Salmonella in food products. Overall, results obtained in this study on naturally contaminated food products highlighted that RTi-PCR without enrichment is a better predictive tool than mini-VIDAS.
引用
收藏
页码:102 / 109
页数:8
相关论文
共 35 条
[1]  
ALTMAN DG, 1994, BMJ-BRIT MED J, V11, P308
[2]  
ALTMAN DG, 1994, BMJ-BRIT MED J, V9, P309
[3]   Epidemiology -: Tracing the origins of Salmonella outbreaks [J].
Bäumler, AJ ;
Hargis, BM ;
Tsolis, RM .
SCIENCE, 2000, 287 (5450) :50-52
[4]   DETECTION OF SALMONELLA SPP IN OYSTERS BY PCR [J].
BEJ, AK ;
MAHBUBANI, MH ;
BOYCE, MJ ;
ATLAS, RM .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1994, 60 (01) :368-373
[5]   A New Real-Time PCR Assay for the Specific Detection of Salmonella spp. Targeting the bipA Gene [J].
Calvo, Laia ;
Martinez-Planells, Asuncion ;
Pardos-Bosch, Joana ;
Garcia-Gil, L. Jesus .
FOOD ANALYTICAL METHODS, 2008, 1 (04) :236-242
[6]   A Rapid and Simple DNA Extraction Procedure to Detect Salmonella spp. and Listeria monocytogenes from Fresh Produce Using Real-time PCR [J].
Chua, Trina ;
Bhagwat, Arvind A. .
FOOD ANALYTICAL METHODS, 2009, 2 (02) :96-101
[7]   Real-time PCR detection of Salmonella in suspect foods from a gastroenteritis outbreak in Kerr County, Texas [J].
Daum, LT ;
Barnes, WJ ;
McAvin, JC ;
Neidert, MS ;
Cooper, LA ;
Huff, WB ;
Gaul, L ;
Riggins, WS ;
Morris, S ;
Salmen, A ;
Lohman, KL .
JOURNAL OF CLINICAL MICROBIOLOGY, 2002, 40 (08) :3050-3052
[8]  
ELIZAQUIVEL P, 2008, J FOOD PROT IN PRESS, V71
[9]  
Eriksson E., 2007, BMC Vet. Res, V3, P21, DOI DOI 10.1186/1746-6148-3-21
[10]   Comparison of cultivation and PCR-hybridization for detection of Salmonella in porcine fecal and water samples [J].
Feder, I ;
Nietfeld, JC ;
Galland, J ;
Yeary, T ;
Sargeant, JM ;
Oberst, R ;
Tamplin, ML .
JOURNAL OF CLINICAL MICROBIOLOGY, 2001, 39 (07) :2477-2484