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Viral Dynamics during Primary Simian Immunodeficiency Virus Infection: Effect of Time-Dependent Virus Infectivity

机译:原始猿猴免疫缺陷病毒感染期间的病毒动力学:时间依赖性病毒感染性的影响。

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摘要

A recent experiment involving simian immunodeficiency virus (SIV) infection of macaques revealed that the infectivity of this virus decreased over the first few months of infection. Based on this observation, we introduce a viral dynamic model in which viral infectivity varies over time. The model is fit to viral load data from eight (donor) monkeys infected by intravaginal inoculation of SIVmac251, three monkeys infected by intravenous inoculation of virus isolated from the donors during the ramp-up phase of acute infection, and three monkeys infected by intravenous inoculation of virus isolated at the viral set-point. Although we only analyze data from 14 monkeys, the new model with time-dependent infectivity seems to fit the data significantly better than a widely used model with constant infectivity (P = 2.44 × 10−11). Our results indicate that plasma virus infectivity on average decays ∼8-fold (95% confidence interval [CI] = 5.1 to 10.3) over the course of acute infection, with the decay occurring exponentially with an average rate of 0.28 day−1 (95% CI = 0.14 to 0.42 day−1). The decay rate in set point plasma virus recipient animals is ∼16 times slower than in ramp-up plasma virus recipient animals and ∼6 times slower than in donor animals. Throughout acute infection up to the set-point, the infection rate is higher in ramp-up plasma virus recipient animals than in set-point plasma virus recipient animals. These results show that the infectivity depends upon the source of viral infection.
机译:近期发生的猿猴猿猴免疫缺陷病毒(SIV)感染实验表明,该病毒的感染力在感染的头几个月内下降。基于此观察,我们介绍了一种病毒动力学模型,其中病毒感染性随时间变化。该模型适合以下情况的病毒载量数据:来自在阴道内接种SIVmac251感染的八只(供体)猴子,在急性感染的加速阶段从捐献者中分离出的病毒静脉内接种的三只猴子,以及经过静脉接种的三只猴子的病毒载量数据在病毒设定点分离的病毒。尽管我们仅分析了14只猴子的数据,但新的具有时间依赖性传染性的模型似乎比广泛使用的具有恒定传染性的模型(P = 2.44×10 −11 )更适合数据。我们的结果表明,血浆病毒感染性在急性感染过程中平均衰减约8倍(95%置信区间[CI] = 5.1至10.3),衰减呈指数形式,平均发生率为0.28天- 1 (95%CI = 0.14至0.42天 -1 )。设定点血浆病毒受体动物的衰变速率比增加血浆病毒受体动物的衰变速率慢约16倍,比供体动物慢约6倍。在直至设定点的急性感染中,增加血浆病毒受体动物的感染率要高于设定血浆病毒受体动物的感染率。这些结果表明,传染性取决于病毒感染的来源。

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