Huang Szu-Wei, Wang Sheng-Fan, Lin Yu-Ting, Yen Chia-Hung, Lee Chih-Hao, Wong Wing-Wai, Tsai Hung-Chin, Yang Chia-Jui, Hu Bor-Shen, Lin Yu-Huei, Wang Chin-Tien, Wang Jaang-Jiun, Hu Zixin, Kuritzkes Daniel R, Chen Yen-Hsu, Chen Yi-Ming Arthur
Center for Infectious Disease and Cancer Research (CICAR), Kaohsiung Medical University, Kaohsiung, Taiwan; Institute of Microbiology and Immunology, National Yang-Ming University, Taipei, Taiwan.
Center for Infectious Disease and Cancer Research (CICAR), Kaohsiung Medical University, Kaohsiung, Taiwan; Department of Medical Laboratory Science and Biotechnology, Kaohsiung Medical University, Kaohsiung, Taiwan.
PLoS One. 2014 Dec 11;9(12):e114441. doi: 10.1371/journal.pone.0114441. eCollection 2014.
The circulating recombinant form (CRF) 07_BC is the most prevalent HIV-1 strain among injection drug users (IDUs) in Taiwan. It contains a 7 amino-acid deletion in its p6gag. We conducted a cohort study to compare viral loads and CD4 cell count changes between patients infected with subtype B and CRF07_BC and to elucidate its mechanism. Twenty-one patients infected with CRF07_BC and 59 patients with subtype B were selected from a cohort of 667 HIV-1/AIDS patients whom have been followed up for 3 years. Generalized estimated equation was used to analyze their clinical data and the results showed that patients infected with CRF07_BC had significantly lower viral loads (about 58,000 copies per ml less) than patients with subtype B infection (p = 0.002). The replicative capacity of nine CRF07_BC and four subtype B isolates were compared and the results showed that the former had significantly lower replicative capacity than the latter although all of them were CCR5- tropic and non-syncytium inducing viruses. An HIV-1-NL4-3 mutant virus which contains a 7 amino-acid deletion in p6gag (designated as 7d virus) was generated and its live cycle was investigated. The results showed that 7d virus had significantly lower replication capacity, poorer protease-mediated processing and viral proteins production. Electron microscopic examination of cells infected with wild-type or 7d virus demonstrated that the 7d virus had poorer and slower viral maturation processes: more viruses attached to the cell membrane and higher proportion of immature virions outside the cells. The interaction between p6gag and Alix protein was less efficient in cells infected with 7d virus. In conclusion, patients infected with CRF07_BC had significantly lower viral loads than patients infected with subtype B and it may due to the deletion of 7 amino acids which overlaps with Alix protein-binding domain of the p6gag.
循环重组型(CRF)07_BC是台湾注射吸毒者(IDU)中最普遍的HIV-1毒株。其p6gag存在7个氨基酸的缺失。我们进行了一项队列研究,比较B亚型和CRF07_BC感染患者的病毒载量和CD4细胞计数变化,并阐明其机制。从667例接受了3年随访的HIV-1/AIDS患者队列中,选取了21例CRF07_BC感染患者和59例B亚型患者。采用广义估计方程分析他们的临床数据,结果显示,CRF07_BC感染患者的病毒载量显著低于B亚型感染患者(每毫升约少58,000拷贝)(p = 0.002)。比较了9株CRF07_BC和4株B亚型毒株的复制能力,结果显示,尽管它们均为CCR5嗜性且非合胞体诱导病毒,但前者的复制能力显著低于后者。构建了一种在p6gag中含有7个氨基酸缺失的HIV-1-NL4-3突变病毒(命名为7d病毒),并研究了其生命周期。结果显示,7d病毒的复制能力显著降低,蛋白酶介导的加工和病毒蛋白产生较差。对感染野生型或7d病毒的细胞进行电子显微镜检查表明,7d病毒的病毒成熟过程较差且较慢:更多病毒附着在细胞膜上,细胞外未成熟病毒粒子的比例更高。在感染7d病毒的细胞中,p6gag与Alix蛋白之间的相互作用效率较低。总之,CRF07_BC感染患者的病毒载量显著低于B亚型感染患者,这可能是由于p6gag中与Alix蛋白结合域重叠的7个氨基酸缺失所致。