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使用靶向yst基因的地高辛配体标记探针检测致病性小肠结肠炎耶尔森菌。

Detection of pathogenic Yersinia enterocolitica using a digoxigenin labelled probe targeting the yst gene.

作者信息

Durisin M D, Ibrahim A, Griffiths M W

机构信息

Department of Food Science, University of Guelph, Ontario, Canada.

出版信息

J Appl Microbiol. 1998 Feb;84(2):285-92. doi: 10.1046/j.1365-2672.1998.00344.x.

Abstract

A 145 base pair digoxigenin-d-UTP-labelled probe, specific for pathogenic Yersinia enterocolitica heat-stable enterotoxin yst gene, was prepared by PCR. The probe was used in DNA-DNA colony hybridization and dot-blot hybridization assays. The specificity of the probe was confirmed using 52 strains representing all Yersinia spp., except Y. pestis. Out of a total of 25 Y. enterocolitica strains screened, the probe correctly identified all 18 pathogenic strains. Among the other Yersinia spp. screened, only one strain of Y. kristensenii was positively detected by the yst probe but could be differentiated by its weak signal response as compared with that obtained by pathogenic strains of Y. enterocolitica.

摘要

通过聚合酶链反应(PCR)制备了一种145个碱基对的地高辛配基-d-UTP标记探针,该探针针对致病性小肠结肠炎耶尔森菌热稳定肠毒素yst基因具有特异性。该探针用于DNA-DNA菌落杂交和斑点印迹杂交试验。使用代表除鼠疫耶尔森菌外的所有耶尔森菌属的52株菌株,证实了该探针的特异性。在总共筛选的25株小肠结肠炎耶尔森菌菌株中,该探针正确鉴定了所有18株致病菌株。在筛选的其他耶尔森菌属中,yst探针仅阳性检测到一株克里斯滕森耶尔森菌,但与小肠结肠炎耶尔森菌致病菌株获得的信号反应相比,其信号反应较弱,可据此进行区分。

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