Comas Iñaki, Hailu Elena, Kiros Teklu, Bekele Shiferaw, Mekonnen Wondale, Gumi Balako, Tschopp Rea, Ameni Gobena, Hewinson R Glyn, Robertson Brian D, Goig Galo A, Stucki David, Gagneux Sebastien, Aseffa Abraham, Young Douglas, Berg Stefan
Genomics and Health Unit, FISABIO Public Health, Valencia 46020, Spain; CIBER (Centros de Investigación Biomédica en Red) in Epidemiology and Public Health, Instituto de Salud Carlos III, Madrid 28029, Spain.
Armauer Hansen Research Institute, PO Box 1005, Addis Ababa, Ethiopia.
Curr Biol. 2015 Dec 21;25(24):3260-6. doi: 10.1016/j.cub.2015.10.061. Epub 2015 Dec 10.
Colonial medical reports claimed that tuberculosis (TB) was largely unknown in Africa prior to European contact, providing a "virgin soil" for spread of TB in highly susceptible populations previously unexposed to the disease [1, 2]. This is in direct contrast to recent phylogenetic models which support an African origin for TB [3-6]. To address this apparent contradiction, we performed a broad genomic sampling of Mycobacterium tuberculosis in Ethiopia. All members of the M. tuberculosis complex (MTBC) arose from clonal expansion of a single common ancestor [7] with a proposed origin in East Africa [3, 4, 8]. Consistent with this proposal, MTBC lineage 7 is almost exclusively found in that region [9-11]. Although a detailed medical history of Ethiopia supports the view that TB was rare until the 20(th) century [12], over the last century Ethiopia has become a high-burden TB country [13]. Our results provide further support for an African origin for TB, with some genotypes already present on the continent well before European contact. Phylogenetic analyses reveal a pattern of serial introductions of multiple genotypes into Ethiopia in association with human migration and trade. In place of a "virgin soil" fostering the spread of TB in a previously naive population, we propose that increased TB mortality in Africa was driven by the introduction of European strains of M. tuberculosis alongside expansion of selected indigenous strains having biological characteristics that carry a fitness benefit in the urbanized settings of post-colonial Africa.
殖民时期的医学报告称,在欧洲人接触之前,非洲基本上不存在肺结核(TB),这为结核病在以前未接触过该疾病的高度易感人群中传播提供了一片“处女地”[1,2]。这与最近支持结核病起源于非洲的系统发育模型形成了直接对比[3-6]。为了解决这一明显的矛盾,我们对埃塞俄比亚的结核分枝杆菌进行了广泛的基因组采样。结核分枝杆菌复合群(MTBC)的所有成员都起源于一个共同祖先的克隆扩增[7],推测起源于东非[3,4,8]。与这一推测一致,MTBC谱系7几乎只在该地区被发现[9-11]。尽管埃塞俄比亚的详细病史支持了结核病在20世纪之前很罕见的观点[12],但在过去的一个世纪里,埃塞俄比亚已成为结核病高负担国家[13]。我们的结果为结核病起源于非洲提供了进一步的支持,一些基因型在欧洲人接触之前就已经在非洲大陆存在了。系统发育分析揭示了多种基因型随着人类迁移和贸易相继引入埃塞俄比亚的模式。我们认为,非洲结核病死亡率的上升并非是因为“处女地”促进了结核病在以前未接触过该疾病的人群中的传播,而是由于欧洲结核分枝杆菌菌株的引入,以及具有在殖民后非洲城市化环境中具有适应性优势的特定本土菌株的扩张。