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通过聚合酶链反应鉴定尿路致病性大肠杆菌中的S、F1C和三种PapG菌毛粘附素。

Identification of S, F1C and three PapG fimbrial adhesins in uropathogenic Escherichia coli by polymerase chain reaction.

作者信息

Mitsumori K, Terai A, Yamamoto S, Yoshida O

机构信息

Department of Urology, Faculty of Medicine, Kyoto University, Japan.

出版信息

FEMS Immunol Med Microbiol. 1998 Aug;21(4):261-8. doi: 10.1111/j.1574-695X.1998.tb01173.x.

Abstract

S and F1C fimbrial adhesins often expressed by uropathogenic Escherichia coli are genetically homologous. A multiply primed polymerase chain reaction (PCR) was developed for discriminating the S (sfa) and F1C (foc) fimbrial operons. A total of 270 uropathogenic E coli strains and 80 fecal isolates were examined. PCR specifically detected the sfa and foc alleles in 105 (93%) of 113 sfa/foc+ strains by DNA hybridization. Furthermore, 87% of sfa+ uropathogenic E. coli simultaneously possessed the genes encoding the class III P fimbrial adhesin (prsG(J96)), alpha-hemolysin and cytotoxic necrotizing factor 1. Statistical analysis showed the class II P fimbrial adhesin (papG(IA2)) and F1C fimbria to be associated with high relative virulence in pyelonephritis and cystitis, respectively. The multiply primed PCR developed should be useful for assessing the contribution of the S and F1C fimbriae in the pathogenesis of urinary tract infections.

摘要

尿路致病性大肠杆菌常表达的S和F1C菌毛黏附素在基因上具有同源性。已开发出一种多重引物聚合酶链反应(PCR)用于区分S(sfa)和F1C(foc)菌毛操纵子。共检测了270株尿路致病性大肠杆菌菌株和80株粪便分离株。通过DNA杂交,PCR在113株sfa/foc+菌株中的105株(93%)中特异性检测到了sfa和foc等位基因。此外,87%的sfa+尿路致病性大肠杆菌同时拥有编码III类P菌毛黏附素(prsG(J96))、α-溶血素和细胞毒性坏死因子1的基因。统计分析表明,II类P菌毛黏附素(papG(IA2))和F1C菌毛分别与肾盂肾炎和膀胱炎的高相对毒力相关。所开发的多重引物PCR对于评估S和F1C菌毛在尿路感染发病机制中的作用应是有用的。

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