Rodgers Mary A, Wilkinson Eduan, Vallari Ana, McArthur Carole, Sthreshley Larry, Brennan Catherine A, Cloherty Gavin, de Oliveira Tulio
Infectious Disease Research, Abbott Diagnostics, Abbott Park, Illinois, USA
Wellcome Trust-Africa Centre for Population Health, University of KwaZulu-Natal, Durban, Republic of South Africa.
J Virol. 2017 Feb 28;91(6). doi: 10.1128/JVI.01841-16. Print 2017 Mar 15.
As the epidemiological epicenter of the human immunodeficiency virus (HIV) pandemic, the Democratic Republic of the Congo (DRC) is a reservoir of circulating HIV strains exhibiting high levels of diversity and recombination. In this study, we characterized HIV specimens collected in two rural areas of the DRC between 2001 and 2003 to identify rare strains of HIV. The gp41 region was sequenced and characterized for 172 HIV-positive specimens. The sequences were predominantly subtype A (43.02%), but 7 other subtypes (33.14%), 20 circulating recombinant forms (CRFs; 11.63%), and 20 unclassified (11.63%) sequences were also found. Of the rare and unclassified subtypes, 18 specimens were selected for next-generation sequencing (NGS) by a modified HIV-switching mechanism at the 5' end of the RNA template (SMART) method to obtain full-genome sequences. NGS produced 14 new complete genomes, which included pure subtype C ( = 2), D ( = 1), F1 ( = 1), H ( = 3), and J ( = 1) genomes. The two subtype C genomes and one of the subtype H genomes branched basal to their respective subtype branches but had no evidence of recombination. The remaining 6 genomes were complex recombinants of 2 or more subtypes, including subtypes A1, F, G, H, J, and K and unclassified fragments, including one subtype CRF25 isolate, which branched basal to all CRF25 references. Notably, all recombinant subtype H fragments branched basal to the H clade. Spatial-geographical analysis indicated that the diverse sequences identified here did not expand globally. The full-genome and subgenomic sequences identified in our study population significantly increase the documented diversity of the strains involved in the continually evolving HIV-1 pandemic. Very little is known about the ancestral HIV-1 strains that founded the global pandemic, and very few complete genome sequences are available from patients in the Congo Basin, where HIV-1 expanded early in the global pandemic. By sequencing a subgenomic fragment of the HIV-1 envelope from study participants in the DRC, we identified rare variants for complete genome sequencing. The basal branching of some of the complete genome sequences that we recovered suggests that these strains are more closely related to ancestral HIV-1 strains than to previously reported strains and is evidence that the local diversification of HIV in the DRC continues to outpace the diversity of global strains decades after the emergence of the pandemic.
作为人类免疫缺陷病毒(HIV)大流行的流行病学中心,刚果民主共和国(DRC)是具有高度多样性和重组性的循环HIV毒株的储存库。在本研究中,我们对2001年至2003年间在刚果民主共和国两个农村地区收集的HIV标本进行了特征分析,以鉴定罕见的HIV毒株。对172份HIV阳性标本的gp41区域进行了测序和特征分析。序列主要为A亚型(43.02%),但也发现了其他7种亚型(33.14%)、20种循环重组型(CRFs;11.63%)和20种未分类序列(11.63%)。在罕见和未分类的亚型中,通过改良的RNA模板5'端HIV转换机制(SMART)方法选择了18份标本进行下一代测序(NGS),以获得全基因组序列。NGS产生了14个新的完整基因组,其中包括纯C亚型(=2)、D亚型(=1)、F1亚型(=1)、H亚型(=3)和J亚型(=1)基因组。两个C亚型基因组和一个H亚型基因组在其各自亚型分支的基部发生分支,但没有重组证据。其余6个基因组是2种或更多亚型的复杂重组体,包括A1、F、G、H、J和K亚型以及未分类片段,其中包括一个CRF25亚型分离株,它在所有CRF25参考序列的基部发生分支。值得注意的是,所有重组的H亚型片段都在H进化枝的基部发生分支。空间地理分析表明,这里鉴定出的多样序列并未在全球范围内扩散。我们在研究人群中鉴定出的全基因组和亚基因组序列显著增加了参与不断演变的HIV-1大流行的毒株的记录多样性。关于引发全球大流行的HIV-1祖先毒株知之甚少,而且在HIV-1在全球大流行早期就已传播的刚果盆地,患者的完整基因组序列也非常少。通过对刚果民主共和国研究参与者的HIV-1包膜亚基因组片段进行测序,我们鉴定出了用于全基因组测序的罕见变异体。我们获得的一些完整基因组序列的基部分支表明,这些毒株与HIV-1祖先毒株的关系比与先前报道的毒株更为密切,这证明在大流行出现数十年后,刚果民主共和国HIV的局部多样化仍继续超过全球毒株的多样性。