DETECTION OF UROVIRULENCE FACTORS IN ESCHERICHIA-COLI BY MULTIPLEX POLYMERASE CHAIN-REACTION

被引:232
作者
YAMAMOTO, S
TERAI, A
YURI, K
KURAZONO, H
TAKEDA, Y
YOSHIDA, O
机构
[1] KYOTO UNIV,FAC MED,DEPT MICROBIOL,SAKYO KU,KYOTO 60601,JAPAN
[2] KYOTO UNIV,FAC MED,DEPT UROL,SAKYO KU,KYOTO 60601,JAPAN
[3] DAINIPPON PHARMACEUT CO LTD,CHUO KU,OSAKA 541,JAPAN
[4] INT MED CTR JAPAN,RES INST,SHINJUKU KU,TOKYO 162,JAPAN
来源
FEMS IMMUNOLOGY AND MEDICAL MICROBIOLOGY | 1995年 / 12卷 / 02期
关键词
ESCHERICHIA COLI; UROVIRULENCE FACTOR; POLYMERASE CHAIN REACTION (PCR);
D O I
10.1016/0928-8244(95)00053-A
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Primers to amplify the genes encoding the virulence factors of uropathogenic Escherichia coli, such as pilus associated with pyelonephritis (pap), haemolysin (hly), aerobactin (aer) and cytotoxic necrotizing factor 1 (cnf1) genes, were designed, The above primers along with previously reported primers for S fimbriae(sfa) and afimbrial adhesin I (afaI) genes were combined to develop a multiplex polymerase chain reaction (PCR) for detection of the respective virulence factors and for the identification of uropathogenic E. coli. The multiplex PCR to detect pap, sfa, afaI, hly, aer and cnf1 genes was highly specific and the sensitivity was found to be about 5 x 10(3) colony forming units of E. coli per mi. A total of 194 E. coli strains isolated from patients with simple acute cystitis were examined by the multiplex PCR and the results were in complete agreement with that obtained by DNA colony hybridization test. The multiplex PCR developed was, therefore, concluded to be a useful, sensitive and rapid assay system to identify uropathogenic E, coli,
引用
收藏
页码:85 / 90
页数:6
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