Brosch R, Gordon S V, Marmiesse M, Brodin P, Buchrieser C, Eiglmeier K, Garnier T, Gutierrez C, Hewinson G, Kremer K, Parsons L M, Pym A S, Samper S, van Soolingen D, Cole S T
Unité de Génétique Moléculaire Bactérienne, Laboratoire de Génomique des Microorganismes Pathogènes, and Centre National de Référence des Mycobactéries, Institut Pasteur, 25-28 Rue du Docteur Roux, 75724 Paris Cedex 15, France.
Proc Natl Acad Sci U S A. 2002 Mar 19;99(6):3684-9. doi: 10.1073/pnas.052548299. Epub 2002 Mar 12.
The distribution of 20 variable regions resulting from insertion-deletion events in the genomes of the tubercle bacilli has been evaluated in a total of 100 strains of Mycobacterium tuberculosis, Mycobacterium africanum, Mycobacterium canettii, Mycobacterium microti, and Mycobacterium bovis. This approach showed that the majority of these polymorphisms did not occur independently in the different strains of the M. tuberculosis complex but, rather, resulted from ancient, irreversible genetic events in common progenitor strains. Based on the presence or absence of an M. tuberculosis specific deletion (TbD1), M. tuberculosis strains can be divided into ancestral and "modern" strains, the latter comprising representatives of major epidemics like the Beijing, Haarlem, and African M. tuberculosis clusters. Furthermore, successive loss of DNA, reflected by region of difference 9 and other subsequent deletions, was identified for an evolutionary lineage represented by M. africanum, M. microti, and M. bovis that diverged from the progenitor of the present M. tuberculosis strains before TbD1 occurred. These findings contradict the often-presented hypothesis that M. tuberculosis, the etiological agent of human tuberculosis evolved from M. bovis, the agent of bovine disease. M. canettii and ancestral M. tuberculosis strains lack none of these deleted regions, and, therefore, seem to be direct descendants of tubercle bacilli that existed before the M. africanum-->M. bovis lineage separated from the M. tuberculosis lineage. This observation suggests that the common ancestor of the tubercle bacilli resembled M. tuberculosis or M. canettii and could well have been a human pathogen already.
在总共100株结核分枝杆菌、非洲分枝杆菌、堪氏分枝杆菌、田鼠分枝杆菌和牛分枝杆菌中,评估了由结核杆菌基因组中插入 - 缺失事件产生的20个可变区的分布情况。这种方法表明,这些多态性中的大多数并非在结核分枝杆菌复合群的不同菌株中独立发生,而是源于共同祖代菌株中古老的、不可逆转的遗传事件。根据是否存在结核分枝杆菌特异性缺失(TbD1),结核分枝杆菌菌株可分为祖先菌株和“现代”菌株,后者包括北京、哈勒姆和非洲结核分枝杆菌簇等主要流行菌株的代表。此外,在非洲分枝杆菌、田鼠分枝杆菌和牛分枝杆菌所代表的进化谱系中,发现了由差异区9和其他后续缺失所反映的DNA连续丢失,该谱系在TbD1出现之前就从当前结核分枝杆菌菌株的祖代中分化出来。这些发现与经常提出的假说相矛盾,该假说认为人类结核病的病原体结核分枝杆菌是由牛病病原体牛分枝杆菌进化而来。堪氏分枝杆菌和祖先结核分枝杆菌菌株没有这些缺失区域中的任何一个,因此,似乎是在非洲分枝杆菌→牛分枝杆菌谱系与结核分枝杆菌谱系分离之前就存在的结核杆菌的直接后代。这一观察结果表明,结核杆菌的共同祖先类似于结核分枝杆菌或堪氏分枝杆菌,很可能已经是一种人类病原体。