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针对鼠伤寒沙门氏菌属的基于DNA的诊断测试,其靶向薄的聚集性菌毛的结构基因agfA。

DNA-based diagnostic tests for Salmonella species targeting agfA, the structural gene for thin, aggregative fimbriae.

作者信息

Doran J L, Collinson S K, Burian J, Sarlós G, Todd E C, Munro C K, Kay C M, Banser P A, Peterkin P I, Kay W W

机构信息

Department of Biochemistry and Microbiology, University of Victoria, British Columbia, Canada.

出版信息

J Clin Microbiol. 1993 Sep;31(9):2263-73. doi: 10.1128/jcm.31.9.2263-2273.1993.

Abstract

Salmonella enteritidis 27655-3b and a few diarrheagenic Escherichia coli strains produce morphologically and antigenically related, thin, aggregative fimbriae, collectively named GVVPQ fimbriae (S. K. Collinson, L. Emödy, T. J. Trust, and W. W. Kay, J. Bacteriol. 174:4490-4495, 1992). To determine whether GVVPQ fimbriae are common to Salmonella spp. and other enteropathogenic members of the family Enterobacteriaceae, 113 isolates were phenotypically screened for Congo red binding and aggregative colony morphology. Presumptive positive and representative negative strains were examined by Western blotting (immunoblotting) by using antiserum to SEF 17, the native GVVPQ fimbria of S. enteritidis. Only four S. enteritidis strains and six E. coli isolates possessed substantial amounts of GVVPQ fimbriae after 24 h of incubation on T medium. Following 5 days of incubation, 56 of 93 Salmonella isolates (60%) and 1 of 7 additional E. coli clinical isolates possessed detectable levels of GVVPQ fimbriae. Since variable expression of GVVPQ fimbriae was observed among Salmonella isolates and some E. coli strains produced scant amounts, as revealed by immunoelectron microscopy, the ability to produce these fimbriae was evaluated by genotypic screening. The structural gene for the SEF 17 fimbrin, agfA, was amplified by the polymerase chain reaction, cloned, and sequenced to provide a characterized DNA probe. An agfA DNA fragment hybridized strongly to 603 of 604 (99.8%) Salmonella isolates but very weakly to 31 of 266 other members of the family Enterobacteriaceae including 26 of 137 E. coli strains, 3 of 14 Citrobacter spp., and single isolates of Shigella sonnei and Enterobacter cloacae. The agfA DNA probe proved to be a valuable diagnostic tool for Salmonella isolates arrayed on hydrophobic grid membrane filters. Unique agfA sequences were targeted in the development of a polymerase chain reaction assay specific for Salmonella spp.

摘要

肠炎沙门氏菌27655 - 3b以及一些致泻性大肠杆菌菌株可产生形态和抗原相关的纤细、凝聚性菌毛,统称为GVVPQ菌毛(S.K. 柯林森、L. 埃莫迪、T.J. 特拉斯特和W.W. 凯,《细菌学杂志》174:4490 - 4495,1992年)。为确定GVVPQ菌毛是否为沙门氏菌属以及肠杆菌科其他肠道致病菌所共有,对113株分离株进行了刚果红结合和凝聚性菌落形态的表型筛选。通过使用抗肠炎沙门氏菌天然GVVPQ菌毛SEF 17的抗血清进行蛋白质印迹法(免疫印迹法)检测推定阳性和代表性阴性菌株。在T培养基上孵育24小时后,仅4株肠炎沙门氏菌菌株和6株大肠杆菌分离株含有大量GVVPQ菌毛。孵育5天后,93株沙门氏菌分离株中的56株(60%)以及另外7株大肠杆菌临床分离株中的1株含有可检测水平的GVVPQ菌毛。由于在沙门氏菌分离株中观察到GVVPQ菌毛表达存在差异,且一些大肠杆菌菌株产生的菌毛量很少,免疫电子显微镜显示了这一点,因此通过基因型筛选评估产生这些菌毛的能力。通过聚合酶链反应扩增、克隆并测序SEF 17菌毛蛋白的结构基因agfA,以提供一个特征化的DNA探针。一个agfA DNA片段与604株沙门氏菌分离株中的603株(99.8%)强烈杂交,但与肠杆菌科其他266个成员中的31株杂交非常弱,其中包括137株大肠杆菌菌株中的26株、14株柠檬酸杆菌属中的3株以及宋内志贺氏菌和阴沟肠杆菌的单个分离株。agfA DNA探针被证明是用于排列在疏水网格膜滤器上的沙门氏菌分离株的一种有价值的诊断工具。在开发针对沙门氏菌属的聚合酶链反应检测方法时,独特的agfA序列成为目标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d45/265745/2e255110138a/jcm00021-0034-a.jpg

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