Department of Veterinary Medicine, University of Cambridge, Cambridge, UK.
J Virol. 2011 Oct;85(19):10332-45. doi: 10.1128/JVI.05290-11. Epub 2011 Jul 27.
Since the demonstration that almost 80% of human immunodeficiency virus type 1 (HIV-1) infections result from the transmission of a single variant from the donor, biological features similar to those of HIV mucosal transmission have been reported for macaques inoculated with simian immunodeficiency virus (SIV). Here we describe the early diversification events and the impact of challenge doses on viral kinetics and on the number of variants transmitted in macaques infected with the chimeric simian/human immunodeficiency virus SHIV(sf162p4). We show that there is a correlation between the dose administered and the number of variants transmitted and that certain inoculum variants are preferentially transmitted. This could provide insight into the viral determinants of transmission and could aid in vaccine development. Challenge through the mucosal route with high doses results in the transmission of multiple variants in all the animals. Such an unrealistic scenario could underestimate potential intervention measures. We thus propose the use of molecular evolution analysis to aid in the determination of challenge doses that better mimic the transmission dynamics seen in natural HIV-1 infection.
自证明近 80%的人类免疫缺陷病毒 1 型(HIV-1)感染是由供体传播的单一变异体引起以来,已报道接种猴免疫缺陷病毒(SIV)的猕猴具有类似于 HIV 粘膜传播的生物学特征。在这里,我们描述了早期多样化事件以及挑战剂量对病毒动力学和感染嵌合猴/人免疫缺陷病毒 SHIV(sf162p4)的猕猴中传播的变异体数量的影响。我们表明,给予的剂量与传播的变异体数量之间存在相关性,并且某些接种物变异体优先传播。这可以深入了解传播的病毒决定因素,并有助于疫苗的开发。通过粘膜途径用高剂量进行挑战会导致所有动物传播多种变异体。这种不切实际的情况可能会低估潜在的干预措施。因此,我们建议使用分子进化分析来辅助确定更能模拟自然 HIV-1 感染中观察到的传播动力学的挑战剂量。