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产肠毒素脆弱拟杆菌与菌血症的关联。

Association of enterotoxigenic Bacteroides fragilis with bacteremia.

作者信息

Kato N, Kato H, Watanabe K, Ueno K

机构信息

Institute of Anaerobic Bacteriology, Gifu University School of Medicine, Japan.

出版信息

Clin Infect Dis. 1996 Dec;23 Suppl 1:S83-6. doi: 10.1093/clinids/23.supplement_1.s83.

Abstract

Polymerase chain reaction (PCR) assay was compared with cell culture assay performed with use of HT29/C1 (human colonic epithelial) cells for identifying strains of enterotoxin-producing Bacteroides fragilis (ETBF) isolated from extraintestinal specimens. A total of 188 unselected strains obtained over 2 years at a central clinical laboratory in Tokyo were tested. Overall, 35 strains (18.6%) were positive by cell culture and PCR assay, 152 strains were negative by both assays, and 1 strain was negative by cell culture assay but positive by the PCR assay; the same results were obtained in repeated assays. Among 64 strains from blood, 18 (28.1%) were ETBF, a rate that was significantly higher (P < .05) than the 17 ETBF (13.7%) among 124 strains from other sites. These results suggest that PCR assay is a simple and reliable tool for detecting ETBF and that enterotoxin may be a virulence factor in bacteremia caused by B. fragilis.

摘要

将聚合酶链反应(PCR)检测法与使用HT29/C1(人结肠上皮)细胞进行的细胞培养检测法相比较,以鉴定从肠外标本中分离出的产肠毒素脆弱拟杆菌(ETBF)菌株。对东京一家中心临床实验室在两年内获得的总共188株未经筛选的菌株进行了检测。总体而言,35株菌株(18.6%)通过细胞培养和PCR检测呈阳性,152株菌株两种检测均为阴性,1株菌株细胞培养检测为阴性但PCR检测为阳性;重复检测得到相同结果。在64株血液来源的菌株中,18株(28.1%)为ETBF,这一比例显著高于其他部位来源的124株菌株中的17株ETBF(13.7%)(P < .05)。这些结果表明,PCR检测法是检测ETBF的一种简单且可靠的工具,并且肠毒素可能是脆弱拟杆菌引起菌血症的一种毒力因子。

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