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首页> 外文期刊>Molecular biology and evolution >Phylogenetic Evidnece for Frequent Positive Selection and Recombination in the Meningococcal Surface Antigen PorB
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Phylogenetic Evidnece for Frequent Positive Selection and Recombination in the Meningococcal Surface Antigen PorB

机译:系统发育的脑膜炎球菌,用于脑膜炎球菌表面抗原PorB中的频繁阳性选择和重组

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摘要

Previous estimates of rates of synonymous (d_s) and nonsynonymous (d_N) substitution among Neisseria meningitidis gene sequences suggested that the surface loops of the variable outer membrane protein PorB were under only weak selection pressure from the host immune response. These findings were consistent with studies indicating that PorB variants were not always protective in immunological and microbiological assays and questioned the suitability of this protein as a vaccine component. PorB, which is expressed at high levels on the surface of the meningococcus, has been implicated in mechanisms of pathogenesis and has also been used as a typing target in epidemiological investigations. In this work, using more precise estimates of selection pressures and recombination rates, we have shown that some residues in the surface loops of PorB are under very strong positive selection, as great as that observed in human immunodeficiency virus-1 surface glycoproteins, whereas amino acids within the loops and the membrane-spanning regions of the protein are under purifying selection, presumably because of structural constraints. Congruence tests showed that recombination occurred at a rate that was not sufficient to erase all phylo-genetic similarly and did not greatly bias selection analysis. Homology models of PorB structure indicated that many strongly selected sites encoded residues that were predicted to be exposed to host immune responses, implying that this protein is under strong immune selection and requires further examination as a potential vaccine candidate. These data show that phylogenetic inference can be used to complement immunological and biochemical data in the choice of vaccine candidates.
机译:先前对脑膜炎奈瑟氏球菌基因序列中同义(d_s)和非同义(d_N)替代率的估计表明,可变外膜蛋白PorB的表面环仅在弱于宿主免疫反应的选择压力下。这些发现与表明PorB变体在免疫学和微生物学分析中并不总是具有保护作用的研究一致,并质疑该蛋白作为疫苗成分的适用性。在脑膜炎球菌表面高水平表达的PorB与发病机理有关,也已被用作流行病学研究中的分型靶标。在这项工作中,使用更精确的选择压力和重组率估算,我们显示了PorB表面环中的某些残基处于非常强的正选择状态,与人类免疫缺陷病毒1表面糖蛋白中观察到的残基一样大,而氨基可能是由于结构限制,蛋白质的环和跨膜区域内的酸正在纯化选择中。一致性测试表明重组发生的速率不足以类似地擦除所有系统发育,并且没有对选择分析产生很大的偏见。 PorB结构的同源性模型表明,许多强烈选择的位点编码的残基被预测会暴露于宿主免疫反应,这表明该蛋白处于强免疫选择状态,需要作为潜在的疫苗候选者进行进一步检查。这些数据表明,系统发育推论可用于补充候选疫苗的免疫学和生化数据。

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