SA MRC Centre for TB Research, Stellenbosch University, Tygerberg, South Africa; DST/NRF Centre of Excellence for Biomedical TB Research, Stellenbosch University, Tygerberg, South Africa; Division of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, Stellenbosch University, Tygerberg, South Africa.
SA MRC Centre for TB Research, Stellenbosch University, Tygerberg, South Africa; DST/NRF Centre of Excellence for Biomedical TB Research, Stellenbosch University, Tygerberg, South Africa; Division of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, Stellenbosch University, Tygerberg, South Africa.
Infect Genet Evol. 2018 Dec;66:361-375. doi: 10.1016/j.meegid.2017.08.021. Epub 2017 Aug 23.
An arms race is an appropriate metaphor to use for the interaction of man and Mycobacterium tuberculosis (M.tb) through the millennia. Estimates of the time of infection of modern humans with M.tb often pre-date the Out-of-Africa migration. Humans have adapted to the changing environment during the migration with respect to climate, food sources and encounters with local pathogens. More recently, there has been adaptation to the demographic changes brought about in the majority of the human population by the Neolithic revolution. By chance and/or selection, specific variants in immune defence have arisen in different population groups. These select for M.tb strains more fit to cause disease and be transmitted, sometimes by exploiting defence systems effective on other bacteria. The different selection pressures on the M.tb lineages carried by specific human groups have resulted in a worldwide M.tb population that is geographically structured according to the humans historically found there. A similar structure is seen with pathogens such as M. leprae and Helicobacter pylori. Modern M.tb strains have emerged which may be more fit, such as the Beijing lineage, leading to their rapid spread both in the areas where they arose, and into new areas after recent introduction. The speed at which this is occurring is outpacing coevolution for the time being. By using the results of genome wide and other association studies, as well as admixture mapping and 'natural experiments' in areas where both a number of populations, admixed populations, and a variety of M.tb strains occur, we can investigate the forces that have driven the coevolution of man and M.tb. The diversity of human and bacterial genetic background may be used in the future to discover and target the specific host-pathogen interactions leading to tuberculosis diseases, which suggests the potential for rational design of vaccines and host-directed therapies.
从几千年的时间来看,人类与结核分枝杆菌(Mycobacterium tuberculosis,M.tb)的相互作用可以用军备竞赛来恰当比喻。现代人类感染 M.tb 的时间估计常常早于走出非洲的迁徙。人类已经适应了在迁徙过程中气候、食物来源和与当地病原体的接触等环境变化。最近,由于新石器时代革命给大多数人类人口带来的人口变化,人类也发生了适应。由于偶然和/或选择,不同人群中出现了特定的免疫防御变体。这些变体选择了更适合引起疾病和传播的 M.tb 菌株,有时是通过利用对其他细菌有效的防御系统。特定人类群体携带的 M.tb 谱系所受到的不同选择压力导致了全球范围内的 M.tb 人群,根据历史上在那里发现的人类进行地理结构划分。M. leprae 和 Helicobacter pylori 等病原体也存在类似的结构。已经出现了一些可能更适合的现代 M.tb 菌株,例如北京谱系,导致它们在出现的地区以及最近引入后进入新地区迅速传播。目前,这种情况的发生速度暂时超过了共同进化。通过使用全基因组和其他关联研究的结果,以及混合人群的混合映射和“自然实验”,以及同时存在多个人群、混合人群和多种 M.tb 菌株的地区,我们可以研究驱动人类和 M.tb 共同进化的力量。人类和细菌遗传背景的多样性将来可能被用于发现和针对导致结核病的特定宿主-病原体相互作用,这表明疫苗和宿主导向疗法的合理设计具有潜力。