Development of a rapid PCR assay specific for Staphylococcus saprophyticus and application to direct detection from urine samples

被引:42
作者
Martineau, F
Picard, FJ
Ménard, C
Roy, PH
Ouellette, M
Bergeron, MG
机构
[1] CHU Quebec, Ctr Rech Infectiol, Quebec City, PQ G1V 4G2, Canada
[2] Univ Laval, Fac Med, Div Microbiol, Quebec City, PQ G1V 4G2, Canada
[3] Univ Laval, Dept Biochim, Ste Foy, PQ G1K 7P4, Canada
关键词
D O I
10.1128/JCM.38.9.3280-3284.2000
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Staphylococcus saprophyticus is one of the most frequently encountered microorganisms associated with acute urinary tract infections (UTIs) in young, sexually active female outpatients. Conventional identification methods based on biochemical characteristics can efficiently identify S. saprophyticus, but the rapidities of these methods need to be improved. Rapid and direct identification of this bacterium from urine samples would be useful to improve time required for the diagnosis of S. saprophyticus infections in the clinical microbiology laboratory, We have developed a PCR-based assay for the specific detection of S. saprophyticus. An arbitrarily primed PCR amplification product of 380 bp specific for S. saprophyticus was sequenced and used to design a set of S. saprophyticus-specific PCR amplification primers. The PCR assay was specific for S. saprophyticus when tested with DNA from 49 gram-positive and 31 gram-negative bacterial species. This assay was also able to amplify efficiently DNA from all 60 strains of S. saprophyticus from various origins tested. This assay was adapted for direct detection from urine samples. The sensitivity levels achieved with urine samples was 19 CFU with 30 cycles of amplification and 0.5 CFU with 40 cycles of amplification. This PCR assay fur the specific detection of S. saprophyticus is simple and rapid (approximately 90 min, including the time for urine specimen preparation).
引用
收藏
页码:3280 / 3284
页数:5
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