Department of Zoology, University of Oxford, South Parks Road, Oxford, OX1 3PS, UK.
Sci Rep. 2017 Jan 23;7:41126. doi: 10.1038/srep41126.
Hyperinvasive lineages of Neisseria meningitidis, which persist despite extensive horizontal genetic exchange, are a major cause of meningitis and septicaemia worldwide. Over the past 50 years one such lineage of meningococci, known as serogroup A, clonal complex 5 (A:cc5), has caused three successive pandemics, including epidemics in sub-Saharan Africa. Although the principal antigens that invoke effective immunity have remained unchanged, distinct A:cc5 epidemic clones have nevertheless emerged. An analysis of whole genome sequence diversity among 153 A:cc5 isolates identified eleven genetic introgression events in the emergence of the epidemic clones, which primarily involved variants of core genes encoding metabolic processes. The acquired DNA was identical to that found over many years in other, unrelated, hyperinvasive meningococci, suggesting that the epidemic clones emerged by acquisition of pre-existing metabolic gene variants, rather than 'virulence' associated or antigen-encoding genes. This is consistent with mathematical models which predict the association of transmission fitness with the emergence and maintenance of virulence in recombining commensal organisms.
脑膜炎奈瑟菌的超强侵袭性谱系尽管存在广泛的水平基因交换,但仍是导致全球脑膜炎和败血症的主要原因。在过去的 50 年中,这种脑膜炎球菌的谱系之一,称为血清群 A、克隆复合体 5(A:cc5),已经引起了三次连续的大流行,包括撒哈拉以南非洲的流行。尽管引起有效免疫的主要抗原保持不变,但不同的 A:cc5 流行克隆已经出现。对 153 株 A:cc5 分离株的全基因组序列多样性分析表明,在流行克隆的出现中发生了 11 次遗传基因渗入事件,主要涉及代谢过程核心基因的变体。获得的 DNA 与多年来在其他不相关的超强侵袭性脑膜炎球菌中发现的 DNA 完全相同,这表明流行克隆的出现是通过获得先前存在的代谢基因变体,而不是与“毒力”相关或抗原编码基因。这与数学模型一致,该模型预测了在重组共生生物中,传播适应性与毒力的出现和维持之间的关联。