Specific and sensitive two-step polymerase chain reaction assay for the detection of Salmonella species

被引:6
作者
Haedicke, W
Wolf, H
Ehret, W
Reischl, U
机构
[1] UNIV REGENSBURG,INST MED MIKROBIOL & HYG,D-93053 REGENSBURG,GERMANY
[2] ZENT KLINIKUM,INST LAB MED,D-86156 AUGSBURG,GERMANY
关键词
D O I
10.1007/BF01709372
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
A polymerase chain reaction (PCR) assay was applied for the selective amplification of a characteristic sequence within a Salmonella-specific chromosomal fragment, A two-temperature PCR cycle enhanced both the speed and overall sensitivity of the amplification procedure, Twenty-one well-characterized Salmonella strains and a number of non-Salmonella strains were tested, With the exception of the rarely isolated Salmonella arizonae strain, the PCR-based approach enabled the specific identification of Salmonella with a detection limit of 10(3) organisms, In combination with a nested PCR assay, as few as ten organisms were detectable, Specificity was demonstrated as no distinct amplification products were detectable with any of the tested non-Salmonella strains, With a pre-enrichment step using paramagnetic anti-Salmonella beads, an increase in sensitivity was observed in the case of clinical samples while the amplification process was not influenced.
引用
收藏
页码:603 / 607
页数:5
相关论文
共 16 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]   FOODBORNE SALMONELLOSIS [J].
BAIRDPARKER, AC .
LANCET, 1990, 336 (8725) :1231-1235
[3]  
BLACKBURN C, 1991, EUROPEAN FOOD DRINK, V15, P35
[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 LISTERIA-MONOCYTOGENES IN CHEESE WITH THE MAGNETIC IMMUNO-POLYMERASE CHAIN-REACTION ASSAY [J].
FLUIT, AC ;
TORENSMA, R ;
VISSER, MJC ;
AARSMAN, CJM ;
POPPELIER, MJJG ;
KELLER, BHI ;
KLAPWIJK, P ;
VERHOEF, J .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1993, 59 (05) :1289-1293
[6]   SALMONELLA-ARIZONA IN THE UNITED-KINGDOM FROM 1966 TO 1990 [J].
HALL, MLM ;
ROWE, B .
EPIDEMIOLOGY AND INFECTION, 1992, 108 (01) :59-65
[7]  
KUHN H, 1994, IMMUN INFEKT, V22, P69
[8]   RAPID ISOLATION OF K88+ ESCHERICHIA-COLI BY USING IMMUNOMAGNETIC PARTICLES [J].
LUND, A ;
HELLEMANN, AL ;
VARTDAL, F .
JOURNAL OF CLINICAL MICROBIOLOGY, 1988, 26 (12) :2572-2575
[9]   ISOLATION OF A SALMONELLA-SPECIFIC DNA HYBRIDIZATION PROBE [J].
OLSEN, JE ;
AABO, S ;
NIELSEN, EO ;
NIELSEN, BB .
APMIS, 1991, 99 (02) :114-120
[10]   MAGNETIC SEPARATION TECHNIQUES IN DIAGNOSTIC MICROBIOLOGY [J].
OLSVIK, O ;
POPOVIC, T ;
SKJERVE, E ;
CUDJOE, KS ;
HORNES, E ;
UGELSTAD, J ;
UHLEN, M .
CLINICAL MICROBIOLOGY REVIEWS, 1994, 7 (01) :43-54