Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
PLoS Pathog. 2012;8(6):e1002786. doi: 10.1371/journal.ppat.1002786. Epub 2012 Jun 21.
In nature, rabies virus (RABV; genus Lyssavirus, family Rhabdoviridae) represents an assemblage of phylogenetic lineages, associated with specific mammalian host species. Although it is generally accepted that RABV evolved originally in bats and further shifted to carnivores, mechanisms of such host shifts are poorly understood, and examples are rarely present in surveillance data. Outbreaks in carnivores caused by a RABV variant, associated with big brown bats, occurred repeatedly during 2001-2009 in the Flagstaff area of Arizona. After each outbreak, extensive control campaigns were undertaken, with no reports of further rabies cases in carnivores for the next several years. However, questions remained whether all outbreaks were caused by a single introduction and further perpetuation of bat RABV in carnivore populations, or each outbreak was caused by an independent introduction of a bat virus. Another question of concern was related to adaptive changes in the RABV genome associated with host shifts. To address these questions, we sequenced and analyzed 66 complete and 20 nearly complete RABV genomes, including those from the Flagstaff area and other similar outbreaks in carnivores, caused by bat RABVs, and representatives of the major RABV lineages circulating in North America and worldwide. Phylogenetic analysis demonstrated that each Flagstaff outbreak was caused by an independent introduction of bat RABV into populations of carnivores. Positive selection analysis confirmed the absence of post-shift changes in RABV genes. In contrast, convergent evolution analysis demonstrated several amino acids in the N, P, G and L proteins, which might be significant for pre-adaptation of bat viruses to cause effective infection in carnivores. The substitution S/T₂₄₂ in the viral glycoprotein is of particular merit, as a similar substitution was suggested for pathogenicity of Nishigahara RABV strain. Roles of the amino acid changes, detected in our study, require additional investigations, using reverse genetics and other approaches.
在自然界中,狂犬病病毒(RABV;属 Lyssavirus,科 Rhabdoviridae)代表了一组与特定哺乳动物宿主物种相关的系统发育谱系。尽管普遍认为 RABV 最初是在蝙蝠中进化而来,然后进一步转移到食肉动物身上,但这种宿主转移的机制知之甚少,在监测数据中也很少有例子。2001-2009 年,亚利桑那州弗拉格斯塔夫地区的食肉动物中反复爆发了一种与大褐蝙蝠相关的 RABV 变体引起的疫情。每次爆发后,都会开展广泛的控制活动,但在接下来的几年中,食肉动物中没有再报告狂犬病病例。然而,仍存在一些问题,即所有的爆发是否都是由蝙蝠 RABV 在食肉动物种群中的单一引入和进一步持续引起的,还是每次爆发都是由蝙蝠病毒的独立引入引起的。另一个令人关注的问题与与宿主转移相关的 RABV 基因组适应性变化有关。为了解决这些问题,我们对来自 Flagstaff 地区和其他类似的由蝙蝠 RABV 引起的食肉动物爆发的 66 个完整和 20 个近乎完整的 RABV 基因组进行了测序和分析,以及北美和全球流行的主要 RABV 谱系的代表。系统发育分析表明,Flagstaff 的每次爆发都是由蝙蝠 RABV 独立引入食肉动物种群引起的。正选择分析证实 RABV 基因在转移后没有发生变化。相比之下,趋同进化分析表明,N、P、G 和 L 蛋白中的几个氨基酸可能对蝙蝠病毒的早期适应具有重要意义,以有效感染食肉动物。病毒糖蛋白中的 S/T₂₄₂ 取代特别重要,因为 Nishigahara RABV 株的致病性也建议了类似的取代。需要使用反向遗传学和其他方法进一步研究我们研究中检测到的氨基酸变化的作用。