Centre for Ecology, Evolution and Environmental Changes (cE3c), Faculdade de Ciências, Universidade de Lisboa, Campo Grande, C2, Room 2.4.11, 1749-016, Lisbon, Portugal.
Biosystems and Integrative Sciences Institute (BioISI), Faculdade de Ciências da Universidade de Lisboa, Lisbon, Portugal.
Sci Rep. 2021 Sep 22;11(1):18789. doi: 10.1038/s41598-021-98226-y.
Genome sequencing has reinvigorated the infectious disease research field, shedding light on disease epidemiology, pathogenesis, host-pathogen interactions and also evolutionary processes exerted upon pathogens. Mycobacterium tuberculosis complex (MTBC), enclosing M. bovis as one of its animal-adapted members causing tuberculosis (TB) in terrestrial mammals, is a paradigmatic model of bacterial evolution. As other MTBC members, M. bovis is postulated as a strictly clonal, slowly evolving pathogen, with apparently no signs of recombination or horizontal gene transfer. In this work, we applied comparative genomics to a whole genome sequence (WGS) dataset composed by 70 M. bovis from different lineages (European and African) to gain insights into the evolutionary forces that shape genetic diversification in M. bovis. Three distinct approaches were used to estimate signs of recombination. Globally, a small number of recombinant events was identified and confirmed by two independent methods with solid support. Still, recombination reveals a weaker effect on M. bovis diversity compared with mutation (overall r/m = 0.037). The differential r/m average values obtained across the clonal complexes of M. bovis in our dataset are consistent with the general notion that the extent of recombination may vary widely among lineages assigned to the same taxonomical species. Based on this work, recombination in M. bovis cannot be excluded and should thus be a topic of further effort in future comparative genomics studies for which WGS of large datasets from different epidemiological scenarios across the world is crucial. A smaller M. bovis dataset (n = 42) from a multi-host TB endemic scenario was then subjected to additional analyses, with the identification of more than 1,800 sites wherein at least one strain showed a single nucleotide polymorphism (SNP). The majority (87.1%) was located in coding regions, with the global ratio of non-synonymous upon synonymous alterations (dN/dS) exceeding 1.5, suggesting that positive selection is an important evolutionary force exerted upon M. bovis. A higher percentage of SNPs was detected in genes enriched into "lipid metabolism", "cell wall and cell processes" and "intermediary metabolism and respiration" functional categories, revealing their underlying importance in M. bovis biology and evolution. A closer look on genes prone to horizontal gene transfer in the MTBC ancestor and included in the 3R (DNA repair, replication and recombination) system revealed a global average negative value for Taijima's D neutrality test, suggesting that past selective sweeps and population expansion after a recent bottleneck remain as major evolutionary drivers of the obligatory pathogen M. bovis in its struggle with the host.
基因组测序为传染病研究领域注入了新的活力,揭示了疾病的流行病学、发病机制、宿主-病原体相互作用以及病原体所经历的进化过程。结核分枝杆菌复合群(MTBC)包含了一种适应动物的成员牛分枝杆菌,可引起陆生哺乳动物的结核病(TB),它是细菌进化的典型模式。与其他 MTBC 成员一样,牛分枝杆菌被假定为一种严格的克隆、缓慢进化的病原体,显然没有重组或水平基因转移的迹象。在这项工作中,我们应用比较基因组学对由来自不同谱系(欧洲和非洲)的 70 株牛分枝杆菌的全基因组序列(WGS)数据集进行了分析,以深入了解塑造牛分枝杆菌遗传多样化的进化力量。我们使用了三种不同的方法来估计重组的迹象。总体而言,通过两种具有可靠支持的独立方法,鉴定并确认了少数重组事件。然而,与突变相比,重组对牛分枝杆菌多样性的影响较弱(总体 r/m=0.037)。在我们的数据集中,牛分枝杆菌不同克隆复合体获得的差异 r/m 平均值与一般概念一致,即重组的程度可能在同一分类物种的不同谱系之间广泛变化。基于这项工作,不能排除牛分枝杆菌中的重组,因此在未来的比较基因组学研究中,应该进一步关注这一问题,而这需要对来自世界各地不同流行情景的大型数据集进行 WGS。然后,对来自多宿主结核病流行情景的较小的牛分枝杆菌数据集(n=42)进行了额外的分析,鉴定出 1800 多个至少有一种菌株显示单核苷酸多态性(SNP)的位点。大多数(87.1%)位于编码区,全球非同义突变与同义突变比值(dN/dS)超过 1.5,表明正选择是对牛分枝杆菌施加的重要进化力量。在“脂质代谢”、“细胞壁和细胞过程”和“中间代谢和呼吸”功能类别中富集的基因中检测到更高百分比的 SNPs,表明它们在牛分枝杆菌生物学和进化中的重要性。对 MTBC 祖先中易发生水平基因转移的基因和包含在 3R(DNA 修复、复制和重组)系统中的基因进行更深入的研究,发现 Tajima's D 中性检验的全球平均值为负值,表明过去的选择清除和近期瓶颈后种群扩张仍然是牛分枝杆菌作为其与宿主斗争的必需病原体的主要进化驱动力。