Comparison of different primers for rapid detection of Salmonella using the polymerase chain reaction

被引:23
作者
Gooding, CM
Choudary, PV
机构
[1] Univ Calif Davis, Dept Entomol, Davis, CA 95616 USA
[2] Univ Calif Davis, Antibody Engn Lab, Davis, CA 95616 USA
关键词
D O I
10.1006/mcpr.1999.0257
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Salmonella is the leading cause of food-borne diarrhoeas in the US. In recent years polymerase chain reaction (PCR) has become the method of choice for rapid and sensitive detection of Salmonellae in contaminated foods. As a result, several different primer sets have been reported for use in PCR-based assay systems, in order to identify an optimal primer set from among the wide range of primers reported in the literature, we synthesized five different pairs and evaluated their relative performance in PCR under uniform assay conditions using a common panel of the target (Salmonella) and non-target (non-Salmonella) bacterial strains. Of the five sets of primers tested, the one designed on the basis of a 199 bp repeat sequence of S. weltevreden [Jitrapakdee et al. (1995) Molecular and Cellular Probes 9, 375-382] gave optimal results with most bacterial strains examined. (C) 1999 Academic Press.
引用
收藏
页码:341 / 347
页数:7
相关论文
共 12 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]   RAPID AND ALTERNATIVE METHODS FOR THE DETECTION OF SALMONELLAS IN FOODS [J].
BLACKBURN, CD .
JOURNAL OF APPLIED BACTERIOLOGY, 1993, 75 (03) :199-214
[3]   Salmonella [J].
Ekperigin, HE ;
Nagaraja, KV .
VETERINARY CLINICS OF NORTH AMERICA-FOOD ANIMAL PRACTICE, 1998, 14 (01) :17-+
[4]   RAPID DETECTION OF SALMONELLAE IN POULTRY WITH THE MAGNETIC IMMUNO-POLYMERASE CHAIN-REACTION ASSAY [J].
FLUIT, AC ;
WIDJOJOATMODJO, MN ;
BOX, ATA ;
TORENSMA, R ;
VERHOEF, J .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1993, 59 (05) :1342-1346
[5]   Detection of Escherichia coli O157:H7 in ground beef in eight hours [J].
Gooding, CM ;
Choudary, PV .
JOURNAL OF MICROBIOLOGICAL METHODS, 1998, 34 (02) :89-98
[6]   Rapid and sensitive immunomagnetic separation-polymerase chain reaction method for the detection of Escherichia coli O157:H7 in raw milk and ice-cream [J].
Gooding, CM ;
Choudary, PV .
JOURNAL OF DAIRY RESEARCH, 1997, 64 (01) :87-93
[7]   A simple, rapid and sensitive detection of Salmonella in food by polymerase chain reaction [J].
Jitrapakdee, S ;
Tassanakajon, A ;
Boonsaeng, V ;
Piankijagum, S ;
Panyim, S .
MOLECULAR AND CELLULAR PROBES, 1995, 9 (06) :375-382
[8]   Use of the polymerase chain reaction for Salmonella detection [J].
Kwang, J ;
Littledike, ET ;
Keen, JE .
LETTERS IN APPLIED MICROBIOLOGY, 1996, 22 (01) :46-51
[9]   High-level secretory expression of immunologically active intact antibody from the yeast Pichia pastoris [J].
Ogunjimi, AA ;
Chandler, JM ;
Gooding, CM ;
Recinos, A ;
Choudary, PV .
BIOTECHNOLOGY LETTERS, 1999, 21 (06) :561-567
[10]   Adsorption of endogenous polyphenols relieves the inhibition by fruit juices and fresh produce of immuno-PCR detection of Escherichia coli O157:H7 [J].
Ogunjimi, AA ;
Choudary, PV .
FEMS IMMUNOLOGY AND MEDICAL MICROBIOLOGY, 1999, 23 (03) :213-220