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脑膜炎奈瑟菌免疫原性自转运蛋白App的鉴定与特性分析

Identification and characterization of App: an immunogenic autotransporter protein of Neisseria meningitidis.

作者信息

Hadi H A, Wooldridge K G, Robinson K, Ala'Aldeen D A

机构信息

Molecular Bacteriology and Immunology Group, Division of Microbiology, School of Clinical Laboratory Sciences, University of Nottingham, Nottingham NG7 2UH, UK.

出版信息

Mol Microbiol. 2001 Aug;41(3):611-23. doi: 10.1046/j.1365-2958.2001.02516.x.

Abstract

In a search for immunogenic virulence factors in Neisseria meningitidis, we have identified a gene encoding a predicted 160 kDa protein with homology to the autotransporter family of proteins. Members of this family are secreted or surface exposed and are often associated with virulence in Gram-negative bacterial pathogens. We named the gene adhesion and penetration protein (app), because of its extensive homology to the hap gene of Haemophilus influenzae. We reconstructed the gene with reference to genomic sequence data and cloned and expressed the protein in Escherichia coli. Rabbit antiserum raised against recombinant App reacted with proteins in all meningococcal isolates examined, which represented clonal groups responsible for the majority of meningococcal invasive disease. Antibodies to the protein were detected in the sera of patients convalescing from meningococcal infection. Purified App had strong stimulating activity for T cells isolated from a number of healthy donors and from one convalescent patient. We confirmed that App is surface localized, cleaved and secreted by N. meningitidis. Importantly, the rabbit anti-App serum killed the organism in the presence of complement. Thus, App is conserved among meningococci, immunogenic in humans and potentially involved in virulence. It therefore merits further investigation as a component of a future multivalent vaccine.

摘要

在寻找脑膜炎奈瑟菌的免疫原性毒力因子的过程中,我们鉴定出一个基因,该基因编码一种预测分子量为160 kDa的蛋白质,与自转运蛋白家族的蛋白质具有同源性。这个家族的成员是分泌型或表面暴露型的,并且常常与革兰氏阴性细菌病原体的毒力相关。由于它与流感嗜血杆菌的hap基因具有广泛的同源性,我们将该基因命名为黏附与穿透蛋白(app)。我们参照基因组序列数据重建了该基因,并在大肠杆菌中克隆和表达了该蛋白质。用重组App免疫家兔产生的抗血清与所有检测的脑膜炎球菌分离株中的蛋白质发生反应,这些分离株代表了导致大多数脑膜炎球菌侵袭性疾病的克隆群。在从脑膜炎球菌感染中康复的患者血清中检测到了针对该蛋白质的抗体。纯化的App对从一些健康供体和一名康复患者分离的T细胞具有强烈的刺激活性。我们证实App定位于脑膜炎奈瑟菌的表面,可被其切割并分泌。重要的是,兔抗App血清在补体存在的情况下可杀死该菌。因此,App在脑膜炎球菌中是保守的,在人类中具有免疫原性,并且可能参与毒力作用。因此,作为未来多价疫苗的一个组成部分,它值得进一步研究。

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