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检测α、β、γ和δ紧密黏附素,这是四种由紧密黏附型微生物病原体表达的紧密黏附素衍生物。

Detection of intimins alpha, beta, gamma, and delta, four intimin derivatives expressed by attaching and effacing microbial pathogens.

作者信息

Adu-Bobie J, Frankel G, Bain C, Goncalves A G, Trabulsi L R, Douce G, Knutton S, Dougan G

机构信息

Department of Biochemistry, Imperial College of Science, Technology and Medicine, London, United Kingdom.

出版信息

J Clin Microbiol. 1998 Mar;36(3):662-8. doi: 10.1128/JCM.36.3.662-668.1998.

Abstract

Intimins are outer membrane proteins expressed by enteric bacterial pathogens capable of inducing intestinal attachment-and-effacement lesions. A eukaryotic cell-binding domain is located within a 280-amino-acid (Int280) carboxy terminus of intimin polypeptides. Polyclonal antiserum was raised against Int280 from enteropathogenic Escherichia coli (EPEC) serotypes O127:H6 and O114:H2 (anti-Int280-H6 and anti-Int280-H2, respectively), and Western blot analysis was used to explore the immunological relationship between the intimin polypeptides expressed by different clinical EPEC and enterohemorrhagic E. coli (EHEC) isolates, a rabbit diarrheagenic E. coli strain (RDEC-1), and Citrobacter rodentium. Anti-Int280-H6 serum reacted strongly with some EPEC serotypes, whereas anti-Int280-H2 serum reacted strongly with strains belonging to different EPEC and EHEC serotypes, RDEC-1, and C. rodentium. These observations were confirmed by using purified Int280 in an enzyme-linked immunosorbent assay and by immunogold and immunofluorescence labelling of whole bacterial cells. Some bacterial strains were recognized poorly by either antiserum (e.g., EPEC O86:H34 and EHEC O157:H7). By using PCR primers designed on the basis of the intimin-encoding eae gene sequences of serotype O127:H6, O114:H2, and O86:H34 EPEC and serotype O157:H7 EHEC, we could distinguish between different eae gene derivatives. Accordingly, the different intimin types were designated alpha, beta, delta, and gamma, respectively.

摘要

紧密黏附素是肠道细菌病原体表达的外膜蛋白,能够诱导肠道黏附-消除性损伤。真核细胞结合结构域位于紧密黏附素多肽280个氨基酸(Int280)的羧基末端。制备了针对肠致病性大肠杆菌(EPEC)O127:H6和O114:H2血清型Int280的多克隆抗血清(分别为抗Int280-H6和抗Int280-H2),并采用蛋白质免疫印迹分析来探究不同临床EPEC和肠出血性大肠杆菌(EHEC)分离株、兔致泻性大肠杆菌菌株(RDEC-1)以及鼠柠檬酸杆菌表达的紧密黏附素多肽之间的免疫关系。抗Int280-H6血清与某些EPEC血清型强烈反应,而抗Int280-H2血清与不同EPEC和EHEC血清型、RDEC-1以及鼠柠檬酸杆菌的菌株强烈反应。通过在酶联免疫吸附测定中使用纯化的Int280以及对全菌细胞进行免疫金和免疫荧光标记,证实了这些观察结果。一些细菌菌株与任何一种抗血清的反应都较弱(例如,EPEC O86:H34和EHEC O157:H7)。通过使用基于O127:H6、O114:H2和O86:H34 EPEC血清型以及O157:H7 EHEC血清型的编码紧密黏附素的eae基因序列设计的PCR引物,我们能够区分不同的eae基因衍生物。因此,不同的紧密黏附素类型分别被命名为α、β、δ和γ。

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Development of a universal intimin antiserum and PCR primers.通用紧密黏附素抗血清和PCR引物的研制。
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