Aaron Diamond AIDS Research Center, 455 First Avenue, 7th Floor, New York, NY 10065, USA.
J Virol. 2010 Dec;84(24):12862-71. doi: 10.1128/JVI.01478-10. Epub 2010 Oct 13.
Fitness disadvantage of the transitional intermediates compared to the initial R5 viruses has been suggested to constitute one of the blockades to coreceptor switching, explaining the late appearance of X4 viruses. Using a simian model for human immunodeficiency virus type 1 (HIV-1) coreceptor switching, we demonstrate in this study that similar molecular evolutionary pathways to coreceptor switch occur in more than one R5 simian/human immunodeficiency virus (SHIV)(SF162P3N)-infected macaque. In infected animals where multiple pathways for expansion or switch to CXCR4 coexist, fitness of the transitional intermediates in coreceptor usage efficiency influences their outgrowth and representation in the infecting virus population. Dualtropic and X4 viruses appear at different disease stages, but they have lower entry efficiency than the coexisting R5 strains, which may explain why they do not outcompete the R5 viruses. Similar observations were made in two infected macaques with coreceptor switch, providing in vivo evidence that fitness disadvantage is an obstacle to X4 emergence and expansion.
与初始 R5 病毒相比,过渡中间体的适应性劣势被认为是阻止辅助受体转换的因素之一,这可以解释 X4 病毒的出现较晚。本研究使用针对人类免疫缺陷病毒 1(HIV-1)辅助受体转换的猴模型,证明在感染 R5 猴/人免疫缺陷病毒(SHIV)(SF162P3N)的猕猴中,存在类似的辅助受体转换的分子进化途径。在存在多种扩展或向 CXCR4 转换途径的感染动物中,辅助受体使用效率中转体中间体的适应性会影响它们在感染病毒群体中的生长和表现。双重嗜性和 X4 病毒出现在不同的疾病阶段,但它们的进入效率低于共存的 R5 株,这可能解释了它们为什么不能与 R5 病毒竞争。在两个发生辅助受体转换的感染猕猴中也观察到了类似的结果,为 X4 的出现和扩展的适应性劣势提供了体内证据。