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A 群脑膜炎奈瑟菌克隆流行期间主要外膜蛋白缺乏抗原多样化及与疾病的关系。

Lack of antigenic diversification of major outer membrane proteins during clonal waves of Neisseria meningitidis serogroup A colonization and disease.

机构信息

Swiss Tropical and Public Health Institute, Basel, Switzerland.

出版信息

Pathog Dis. 2013 Feb;67(1):4-10. doi: 10.1111/2049-632X.12000. Epub 2012 Nov 28.

DOI:10.1111/2049-632X.12000
PMID:23620114
Abstract

In particular in the 'meningitis belt' of sub-Saharan Africa, epidemic meningococcal meningitis is a severe public health problem. In the past decades, serogroup A lineages have been the dominant etiologic agents, but also other serogroups have caused outbreaks. A comprehensive vaccine based on subcapsular outer membrane proteins (OMPs) is not available. Here, we have investigated whether meningococcal populations overcome herd immunity by changing antigenic properties of their OMPs. Meningococcal isolates were collected in the context of longitudinal studies in Ghana between 2002 and 2008 and in Burkina Faso between 2006 and 2007. Serogroup A strains isolated during two clonal waves of colonization and disease showed no diversification in the genes encoding their PorA, PorB, and FetA proteins. However, we detected occasional allelic exchange of opa genes, as well as wide variation in the number of intragenic tandem repeats, showing that phase variation of Opa protein expression is a frequent event. Altogether we observed a remarkable antigenic stability of the PorA, PorB and FetA proteins over years. Our results indicate that while herd immunity may be responsible for the disappearance of meningococcal clones over time, it is not a strong driving force for antigenic diversification of the major OMPs analyzed here.

摘要

特别是在撒哈拉以南非洲的“脑膜炎带”,流行性脑脊髓膜炎是一个严重的公共卫生问题。在过去几十年中,A 群血清型一直是主要的病原体,但其他血清型也引起了暴发。目前还没有基于荚膜表面蛋白(OMP)的综合疫苗。在这里,我们研究了脑膜炎奈瑟菌种群是否通过改变其 OMP 的抗原特性来克服群体免疫。在 2002 年至 2008 年期间在加纳和 2006 年至 2007 年期间在布基纳法索进行的纵向研究中收集了脑膜炎奈瑟菌分离株。在两次克隆波定殖和疾病期间分离的 A 群菌株在其编码 PorA、PorB 和 FetA 蛋白的基因中没有多样化。然而,我们检测到了偶尔的 opa 基因的等位基因交换,以及基因内串联重复的广泛变化,表明 Opa 蛋白表达的相位变异是一个频繁发生的事件。总的来说,我们观察到 PorA、PorB 和 FetA 蛋白的抗原稳定性在数年内非常显著。我们的结果表明,虽然群体免疫可能是导致脑膜炎奈瑟菌克隆随时间消失的原因,但它不是分析的主要 OMP 抗原多样化的强大驱动力。

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