Laboratory of Molecular Virology and Epidemiology, AIDS Research Center, National Institute of Infectious Diseases, Shinjuku-ku, Tokyo, Japan.
PLoS One. 2009 Aug 18;4(8):e6666. doi: 10.1371/journal.pone.0006666.
A growing number of emerging HIV-1 recombinants classified as circulating recombinant forms (CRFs) have been identified in Southeast Asia in recent years, establishing a molecular diversity of increasing complexity in the region. Here, we constructed a replication-competent HIV-1 clone for CRF33_01B (designated p05MYKL045.1), a newly identified recombinant comprised of CRF01_AE and subtype B. p05MYKL045.1 was reconstituted by cloning of the near full-length HIV-1 sequence from a newly-diagnosed individual presumably infected heterosexually in Kuala Lumpur, Malaysia. The chimeric clone, which contains the 5' LTR (long terminal repeat) region of p93JP-NH1 (a previously isolated CRF01_AE infectious clone), showed robust viral replication in the human peripheral blood mononuclear cells. This clone demonstrated robust viral propagation and profound syncytium formation in CD4+, CXCR4-expressing human glioma NP-2 cells, indicating that p05MYKL045.1 is a CXCR4-using virus. Viral propagation, however, was not detected in various human T cell lines including MT-2, M8166, Sup-T1, H9, Jurkat, Molt-4 and PM1. p05MYKL045.1 appears to proliferate only in restricted host range, suggesting that unknown viral and/or cellular host factors may play a role in viral infectivity and replication in human T cell lines. Availability of a CRF33_01B molecular clone will be useful in facilitating the development of vaccine candidates that match the HIV-1 strains circulating in Southeast Asia.
近年来,东南亚地区发现了越来越多的新型 HIV-1 重组病毒,被归类为循环重组形式(CRF),这表明该地区的 HIV-1 分子多样性变得越来越复杂。在这里,我们构建了一个具有复制能力的 HIV-1 克隆,用于 CRF33_01B(命名为 p05MYKL045.1),这是一种新发现的重组病毒,由 CRF01_AE 和 B 亚型组成。p05MYKL045.1 是通过从马来西亚吉隆坡的一个新诊断的个体中克隆全长 HIV-1 序列而重新构建的,该个体可能是通过异性性行为感染的。该嵌合克隆包含了 p93JP-NH1 的 5'LTR(长末端重复序列)区域(之前分离到的 CRF01_AE 感染性克隆),在人外周血单核细胞中显示出强大的病毒复制能力。该克隆在表达 CXCR4 的人胶质细胞瘤 NP-2 细胞中表现出强大的病毒增殖和明显的合胞体形成能力,表明 p05MYKL045.1 是一种 CXCR4 利用型病毒。然而,在各种人类 T 细胞系中,包括 MT-2、M8166、Sup-T1、H9、Jurkat、Molt-4 和 PM1,均未检测到病毒的增殖。p05MYKL045.1 似乎仅在有限的宿主范围内增殖,这表明未知的病毒和/或细胞宿主因素可能在人类 T 细胞系中的病毒感染和复制中发挥作用。CRF33_01B 分子克隆的出现将有助于开发与东南亚流行的 HIV-1 株相匹配的疫苗候选物。