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多重聚合酶链反应检测产志贺毒素大肠杆菌O157:H7

Detection of verotoxin-producing Escherichia coli O157:H7 by multiplex polymerase chain reaction.

作者信息

Nagano I, Kunishima M, Itoh Y, Wu Z, Takahashi Y

机构信息

Department of Parasitology, Gifu University School of Medicine, Japan.

出版信息

Microbiol Immunol. 1998;42(5):371-6. doi: 10.1111/j.1348-0421.1998.tb02297.x.

Abstract

We constructed primers for multiplex polymerase chain reaction (PCR) to detect verotoxin-producing Escherichia coli (VTEC) O157:H7. The multiplex PCR primers were designed from the sequence of the flagellin structural gene of Escherichia coli flagellar type H7 (GenBank under accession number L07388), and from the sequence of the rfbE gene of Escherichia coli O157:H7 (GenBank under accession number S83460). In addition to these primers, we used a primer pair reported by Karch and Meyer (J. Clin. Microbiol. 27: 2751-2757, 1989) to amplify various VT genes from VTEC. All of the examined specimens (18 isolates) of VT-producing E. coli O157:H7 showed a positive result by the multiplex PCR test with the three sets of primers. The sensitivity of detection for VT-producing E. coli O157:H7 was shown to be at least 3,000 cells per PCR tube.

摘要

我们构建了用于多重聚合酶链反应(PCR)的引物,以检测产志贺毒素大肠杆菌(VTEC)O157:H7。多重PCR引物是根据大肠杆菌H7鞭毛型鞭毛蛋白结构基因的序列(GenBank登录号为L07388)以及大肠杆菌O157:H7的rfbE基因序列(GenBank登录号为S83460)设计的。除了这些引物外,我们还使用了Karch和Meyer报道的一对引物(《临床微生物学杂志》27: 2751 - 2757, 1989)从VTEC中扩增各种VT基因。所有检测的产志贺毒素大肠杆菌O157:H7标本(18个分离株)通过使用这三组引物进行的多重PCR检测均呈阳性结果。产志贺毒素大肠杆菌O157:H7的检测灵敏度显示为每PCR管至少3000个细胞。

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