Sampathkumar Raghavan, Shadabi Elnaz, Luo Ma
Department of Medical Microbiology, University of Manitoba, Winnipeg, MB, Canada R3E 0J9.
Adv Virol. 2012;2012:508967. doi: 10.1155/2012/508967. Epub 2012 May 16.
As of February 2012, 50 circulating recombinant forms (CRFs) have been reported for HIV-1 while one CRF for HIV-2. Also according to HIV sequence compendium 2011, the HIV sequence database is replete with 414,398 sequences. The fact that there are CRFs, which are an amalgamation of sequences derived from six or more subtypes (CRF27_cpx (cpx refers to complex) is a mosaic with sequences from 6 different subtypes besides an unclassified fragment), serves as a testimony to the continual divergent evolution of the virus with its approximate 1% per year rate of evolution, and this phenomena per se poses tremendous challenge for vaccine development against HIV/AIDS, a devastating disease that has killed 1.8 million patients in 2010. Here, we explore the interaction between HIV-1 and host genetic variation in the context of HIV/AIDS and antiretroviral therapy response.
截至2012年2月,已报告了50种HIV-1的循环重组形式(CRF),而HIV-2只有1种CRF。同样根据《2011年HIV序列汇编》,HIV序列数据库中存有414,398条序列。存在CRF这一事实,即由六种或更多亚型的序列融合而成(CRF27_cpx(cpx指复杂型)除了一个未分类片段外,是来自6种不同亚型序列的镶嵌体),证明了该病毒以每年约1%的进化速率持续发生分化进化,而这一现象本身就给针对艾滋病(一种在2010年已导致180万患者死亡的毁灭性疾病)的疫苗研发带来了巨大挑战。在此,我们在艾滋病及抗逆转录病毒治疗反应的背景下,探讨HIV-1与宿主基因变异之间的相互作用。