Zimpel Cristina Kraemer, Patané José Salvatore L, Guedes Aureliano Coelho Proença, de Souza Robson F, Silva-Pereira Taiana T, Camargo Naila C Soler, de Souza Filho Antônio F, Ikuta Cássia Y, Neto José Soares Ferreira, Setubal João Carlos, Heinemann Marcos Bryan, Guimaraes Ana Marcia Sa
Laboratory of Applied Research in Mycobacteria, Department of Microbiology, Institute of Biomedical Sciences, University of São Paulo, São Paulo, Brazil.
Department of Preventive Veterinary Medicine and Animal Health, School of Veterinary Medicine and Animal Sciences, University of São Paulo, São Paulo, Brazil.
Front Microbiol. 2020 May 7;11:843. doi: 10.3389/fmicb.2020.00843. eCollection 2020.
is the main causative agent of zoonotic tuberculosis in humans and frequently devastates livestock and wildlife worldwide. Previous studies suggested the existence of genetic groups of strains based on limited DNA markers (a.k.a. clonal complexes), and the evolution and ecology of this pathogen has been only marginally explored at the global level. We have screened over 2,600 publicly available genomes and newly sequenced four wildlife strains, gathering 1,969 genomes from 23 countries and at least 24 host species, including humans, to complete a phylogenomic analyses. We propose the existence of four distinct global lineages of (Lb1, Lb2, Lb3, and Lb4) underlying the current disease distribution. These lineages are not fully represented by clonal complexes and are dispersed based on geographic location rather than host species. Our data divergence analysis agreed with previous studies reporting independent archeological data of ancient (South Siberian infected skeletons at ∼2,000 years before present) and indicates that extant originated between 715 and 3,556 years BP, with later emergence in the New World and Oceania, likely influenced by trades among countries.
是人类人畜共患结核病的主要病原体,经常在全球范围内破坏牲畜和野生动物。先前的研究表明,基于有限的DNA标记(又称克隆复合体)存在菌株的遗传群体,并且这种病原体的进化和生态在全球层面上仅得到了很少的探索。我们筛选了2600多个公开可用的基因组,并新测序了4个野生动物菌株,从23个国家和至少24种宿主物种(包括人类)收集了1969个基因组,以完成系统发育基因组分析。我们提出,在当前疾病分布的基础上存在四种不同的全球谱系(Lb1、Lb2、Lb3和Lb4)。这些谱系不能完全由克隆复合体来代表,并且是根据地理位置而不是宿主物种分散的。我们的数据分歧分析与先前报告古代(约2000年前南西伯利亚受感染骨骼)独立考古数据的研究一致,并表明现存的起源于公元前715年至3556年之间,后来在新世界和大洋洲出现,可能受到国家间贸易的影响。