Tongo Marcel, Harkins Gordon W, Dorfman Jeffrey R, Billings Erik, Tovanabutra Sodsai, de Oliveira Tulio, Martin Darren P
KwaZulu-Natal Research Innovation and Sequencing Platform (Krisp), School of Laboratory Medicine and Medical Sciences, College of Health Sciences, Nelson R Mandela School of Medicine, University of KwaZulu-Natal, Durban 4041, South Africa.
Division of Computational Biology, Department of Integrative Biomedical Sciences and Institute of Infectious Disease and Molecular Medicine, Faculty of Health Sciences, University of Cape Town, Cape Town 7925, South Africa.
Virus Evol. 2018 Feb 19;4(1):vey003. doi: 10.1093/ve/vey003. eCollection 2018 Jan.
Subtype A is one of the rare HIV-1 group M (HIV-1M) lineages that is both widely distributed throughout the world and persists at high frequencies in the Congo Basin (CB), the site where HIV-1M likely originated. This, together with its high degree of diversity suggests that subtype A is amongst the fittest HIV-1M lineages. Here we use a comprehensive set of published near full-length subtype A sequences and A-derived genome fragments from both circulating and unique recombinant forms (CRFs/URFs) to obtain some insights into how frequently these lineages have independently seeded HIV-1M sub-epidemics in different parts of the world. We do this by inferring when and where the major subtype A lineages and subtype A-derived CRFs originated. Following its origin in the CB during the 1940s, we track the diversification and recombination history of subtype A sequences before and during its dissemination throughout much of the world between the 1950s and 1970s. Collectively, the timings and numbers of detectable subtype A recombination and dissemination events, the present broad global distribution of the sub-epidemics that were seeded by these events, and the high prevalence of subtype A sequences within the regions where these sub-epidemics occurred, suggest that ancestral subtype A viruses (and particularly sub-subtype A1 ancestral viruses) may have been genetically predisposed to become major components of the present epidemic.
A亚型是罕见的HIV-1 M组(HIV-1M)谱系之一,它在全球广泛分布,并在刚果盆地(CB)以高频率持续存在,而刚果盆地可能是HIV-1M的起源地。这一点,连同其高度的多样性表明,A亚型是适应性最强的HIV-1M谱系之一。在这里,我们使用了一组全面的已发表的近全长A亚型序列以及来自循环型和独特重组型(CRF/URF)的A亚型衍生基因组片段,以深入了解这些谱系在世界不同地区独立引发HIV-1M子流行的频率。我们通过推断主要A亚型谱系和A亚型衍生的CRF的起源时间和地点来做到这一点。在20世纪40年代起源于刚果盆地之后,我们追踪了A亚型序列在20世纪50年代至70年代在世界大部分地区传播之前和期间的多样化和重组历史。总体而言,可检测到的A亚型重组和传播事件的时间和数量、这些事件引发的子流行目前在全球的广泛分布,以及这些子流行发生地区内A亚型序列的高流行率,表明A亚型祖先病毒(特别是A1亚亚型祖先病毒)可能在基因上就倾向于成为当前流行的主要组成部分。