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质粒在1型痢疾志贺氏菌菌株毒力相关特性及O抗原表达中的作用。

Role of plasmids in virulence-associated attributes and in O-antigen expression in Shigella dysenteriae type 1 strains.

作者信息

Haider K, Azad A K, Qadri F, Nahar S, Ciznar I

机构信息

International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka.

出版信息

J Med Microbiol. 1990 Sep;33(1):1-9. doi: 10.1099/00222615-33-1-1.

Abstract

The association of plasmids with virulence characters and O-antigen expression was studied in two virulent and seven avirulent mutant strains of Shigella dysenteriae type 1. Deletion of a 12-Mda segment from a 140-Mda plasmid in two smooth avirulent mutants made the derivatives avirulent in the Sereny test and non-invasive in HeLa cells. The mutants were unable to bind Congo red, and did not express the virulence marker antigen. Mutants completely lacking the 140-Mda plasmid also showed similar avirulent characters. However, rough mutants retained the ability to bind Congo red. Our results indicate that the essential gene(s) for virulence may be located on the 140-Mda plasmid, a small deletion from which may lead to avirulence. This deletion did not affect the protein antigen expression nor change their antigenicity. Analysis of lipopolysaccharide (LPS) patterns showed that strains containing the 6-Mda plasmid produced the complete LPS and were smooth, whereas strains containing either the 140- or a 4- or 2-Mda plasmid, in the absence of the 6-Mda plasmid, produced smaller amounts of O antigen and were rough. Western-blot analysis and crossed immuno-electrophoresis gave similar results. The 140-, 4-, or 2-Mda plasmid, in the absence of the 6-Mda plasmid, may code for non-specific galactosyl transferase-like activity which can add, non-specifically and at a reduced level, the galactose residue (the first sugar in the O antigen repeat unit) to the LPS core.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在两株强毒株和七株1型痢疾志贺氏菌无毒突变株中研究了质粒与毒力特性及O抗原表达的关联。两个光滑无毒突变株中140兆达尔质粒上一个12兆达尔片段的缺失,使衍生株在塞雷尼试验中无毒且对HeLa细胞无侵袭性。这些突变株无法结合刚果红,也不表达毒力标记抗原。完全缺失140兆达尔质粒的突变株也表现出类似的无毒特性。然而,粗糙型突变株仍保留结合刚果红的能力。我们的结果表明,毒力必需基因可能位于140兆达尔质粒上,该质粒上的一个小缺失可能导致无毒。这种缺失不影响蛋白质抗原表达,也不改变其抗原性。脂多糖(LPS)模式分析表明,含有6兆达尔质粒的菌株产生完整的LPS且表面光滑,而在没有6兆达尔质粒的情况下,含有140兆达尔或4兆达尔或2兆达尔质粒的菌株产生较少的O抗原且表面粗糙。蛋白质免疫印迹分析和交叉免疫电泳得出了类似结果。在没有6兆达尔质粒的情况下,140兆达尔、4兆达尔或2兆达尔质粒可能编码非特异性半乳糖基转移酶样活性,该活性可将半乳糖残基(O抗原重复单元中的第一个糖)非特异性且以较低水平添加到LPS核心上。(摘要截短于250字)

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