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由不同vaa基因编码的人型支原体粘附素大小和抗原变异的分子基础。

Molecular basis of size and antigenic variation of a Mycoplasma hominis adhesin encoded by divergent vaa genes.

作者信息

Zhang Q, Wise K S

机构信息

Department of Molecular Microbiology and Immunology, School of Medicine, University of Missouri-Columbia 65212, USA.

出版信息

Infect Immun. 1996 Jul;64(7):2737-44. doi: 10.1128/iai.64.7.2737-2744.1996.

Abstract

The molecular basis for the size and antigenic diversity of the variable adherence-associated (Vaa) antigen, a major surface protein and a putative adhesin (of Mycoplasma hominis, is described. Size-variant alleles of the single-copy vaa gene encode abundant surface lipoproteins containing one to four nearly identical, tandem repetitive units of 121 amino acids in the central region of the mature Vaa product. Gain or loss of central repeats in vaa genes gives rise to distinct size-variant Vaa antigens in clonal populations of this organism. The N-terminal and repeat regions of Vaa contain highly conserved sequences, while the C-terminal region, implicated as the adherence-mediating module, is highly variable and divergent among different strains of this pathogen. Sequence variation in this region may underlie the strain-dependent binding of some monoclonal antibodies to Vaa products. The Vaa antigen is expressed in vivo during chronic, active arthritis associated with M. hominis infection and is highly immunogenic in the human host. Size variation and C-terminal antigenic divergence of Vaa could affect the adherence of M. hominis and evasion of antibody-mediated immunity, thereby contributing to the organism's adaptive capability in the human host. Variation in vaa genes reveals a distinct pattern of mutations generating mycoplasma surface variation.

摘要

本文描述了可变黏附相关(Vaa)抗原的大小和抗原多样性的分子基础,Vaa抗原是一种主要的表面蛋白,也是人型支原体的一种假定黏附素。单拷贝vaa基因的大小变异等位基因编码丰富的表面脂蛋白,在成熟Vaa产物的中心区域含有一至四个几乎相同的121个氨基酸的串联重复单元。vaa基因中中心重复序列的增减导致该生物体克隆群体中出现不同大小变异的Vaa抗原。Vaa的N端和重复区域包含高度保守的序列,而作为黏附介导模块的C端区域高度可变,在该病原体的不同菌株之间存在差异。该区域的序列变异可能是一些单克隆抗体与Vaa产物的菌株依赖性结合的基础。Vaa抗原在与人类支原体感染相关的慢性活动性关节炎期间在体内表达,并且在人类宿主中具有高度免疫原性。Vaa的大小变异和C端抗原差异可能影响人型支原体的黏附以及逃避抗体介导的免疫,从而有助于该生物体在人类宿主中的适应能力。vaa基因的变异揭示了产生支原体表面变异的独特突变模式。

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