Polymerase Chain Reaction for the Rapid Detection and Serovar Identification of Salmonella in Food and Feeding Stuff

被引:48
作者
Malorny, Burkhard [1 ]
Huehn, Stephan [1 ]
Dieckmann, Ralf [1 ]
Kraemer, Nadine [1 ]
Helmuth, Reiner [1 ]
机构
[1] Fed Inst Risk Assessment, Natl Salmonella Reference Lab, D-12277 Berlin, Germany
关键词
Salmonella; Detection; Rapid Methods; Food; Feed; Serovar Identification; Real-time PCR; REAL-TIME PCR; MULTIPLEX PCR; IMMUNOMAGNETIC SEPARATION; MULTICENTER VALIDATION; REACTION ASSAY; SELECTIVE AMPLIFICATION; DIAGNOSTIC PCR; GENE SEQUENCE; FECAL SAMPLES; ENTERICA;
D O I
10.1007/s12161-008-9057-9
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
The polymerase chain reaction (PCR) is one of the most important rapid methods for the sensitive and specific detection of pathogenic and spoilage microorganisms. The method is increasingly applied in surveillance and monitoring programs to detect pathogens, especially for ensuring the safety and quality of food. The food-borne pathogen Salmonella together with Campylobacter is the most predominant bacterial pathogen in Europe, causing approximately 160,000 confirmed human cases per year. During the last two decades, the importance of Salmonella for food safety triggered the development of dozens of PCR-based detection methods. They promise significant advantages compared to the traditional culture-based methods with respect to speed, easiness, reliability, sensitivity, cost effectiveness, and automation. However, many of them are not applicable because of lacking validation procedures. Meanwhile, PCR has internationally been standardized and guidelines as well as standards for the validation of alternative methods, such as PCR, were established. This review will give an overview of the historical development of PCR-based methods for the detection of Salmonella including validation aspects and summarizes the state-of-the-art for the detection of Salmonella in food and feeding stuff by real-time PCR. Furthermore, current multiplex PCR-based serovar-specific identification methods will be reviewed.
引用
收藏
页码:81 / 95
页数:15
相关论文
共 133 条
[1]   SALMONELLA IDENTIFICATION BY THE POLYMERASE CHAIN-REACTION [J].
AABO, S ;
RASMUSSEN, OF ;
ROSSEN, L ;
SORENSEN, PD ;
OLSEN, JE .
MOLECULAR AND CELLULAR PROBES, 1993, 7 (03) :171-178
[2]   Effects of amplification facilitators on diagnostic PCR in the presence of blood, feces, and meat [J].
Abu Al-Soud, W ;
Rådström, P .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (12) :4463-4470
[3]   Efficient priming of PCR with short oligonucleotides conjugated to a minor groove binder [J].
Afonina, I ;
Zivarts, M ;
Kutyavin, I ;
Lukhtanov, E ;
Gamper, H ;
Meyer, RB .
NUCLEIC ACIDS RESEARCH, 1997, 25 (13) :2657-2660
[4]   Identification by subtractive hybridization of sequences specific for Salmonella enterica serovar Enteritidis [J].
Agron, PG ;
Walker, RL ;
Kinde, H ;
Sawyer, SJ ;
Hayes, DC ;
Wollard, J ;
Andersen, GL .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2001, 67 (11) :4984-4991
[5]  
[Anonymous], 2003, 161402003 ISO
[6]  
[Anonymous], 2007, AMTLICHE SAMMLUNG UN
[7]  
[Anonymous], 2007, 65792002AMD12007 EN
[8]  
[Anonymous], 2005, 208362005 ISOTS
[9]  
[Anonymous], 2005, 221742005 ISO
[10]   Salmonella serovar identification using PCR-based detection of gene presence and absence [J].
Arrach, Nabil ;
Porwollik, Steffen ;
Cheng, Pui ;
Cho, Ann ;
Long, Fred ;
Choi, Sang-Ho ;
McClelland, Michael .
JOURNAL OF CLINICAL MICROBIOLOGY, 2008, 46 (08) :2581-2589