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流感嗜血杆菌中脂多糖表位表达的染色体位点鉴定。

Identification of a chromosomal locus for expression of lipopolysaccharide epitopes in Haemophilus influenzae.

作者信息

Weiser J N, Lindberg A A, Manning E J, Hansen E J, Moxon E R

机构信息

Oxford University, Department of Paediatrics, United Kingdom.

出版信息

Infect Immun. 1989 Oct;57(10):3045-52. doi: 10.1128/iai.57.10.3045-3052.1989.

Abstract

Lipopolysaccharide (LPS) is a major virulence determinant of Haemophilus influenzae. The organism is able to display an extensive repertoire of different LPS structures through the loss and acquisition of multiple oligosaccharide epitopes in various combinations. This marked heterogeneity of LPS molecules has complicated the analysis of the structure of LPS and its role in pathogenesis. A genomic library was screened for the ability to transform H. influenzae to express novel LPS epitopes defined by reactivity with oligosaccharide specific monoclonal antibodies. A chromosomal locus, lic-1, involved in expression of at least three different epitopes (recognized by monoclonal antibodies 4C4, 12D9, and 6A2), was identified on a 5.6-kilobase restriction endonuclease fragment. Transformation of H. influenzae with subclones from within lic-1 was used to generate a series of isogenic and phenotypic variants. All transformants displayed phase variation for their newly acquired epitopes. Altered binding specificities of LPS with monoclonal antibodies correlated with changes in sugar compositional analysis. The expression of two epitopes was eliminated by introduction of site-specific mutations in lic-1, confirming the role of lic-1 in oligosaccharide biosynthesis.

摘要

脂多糖(LPS)是流感嗜血杆菌的主要毒力决定因素。该生物体能够通过多种寡糖表位以不同组合的丢失和获得来展现出广泛多样的不同LPS结构。LPS分子的这种显著异质性使LPS结构分析及其在发病机制中的作用变得复杂。对一个基因组文库进行筛选,以寻找将流感嗜血杆菌转化为能够表达由与寡糖特异性单克隆抗体反应所定义的新型LPS表位的能力。在一个5.6千碱基的限制性内切酶片段上鉴定出一个与至少三种不同表位(被单克隆抗体4C4、12D9和6A2识别)表达相关的染色体位点lic-1。用来自lic-1内部的亚克隆对流感嗜血杆菌进行转化,以产生一系列同基因和表型变异体。所有转化体对于其新获得的表位均表现出相变。LPS与单克隆抗体结合特异性的改变与糖成分分析的变化相关。通过在lic-1中引入位点特异性突变消除了两种表位的表达,证实了lic-1在寡糖生物合成中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7301/260768/d2c209a0e7bc/iai00070-0132-a.jpg

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