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Determination of virus burst size in vivo using a single-cycle SIV in rhesus macaques

机译:使用单周期SIV测定猕猴体内的病毒爆发大小

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摘要

A single-cycle simian immunodeficiency virus (scSIV) that undergoes only one round of infection and replication was constructed to calculate the total number of virons produced by an SIV-infected cell in vivo. Four Mamu-A*01 rhesus macaques were inoculated on two occasions 11 weeks apart with the scSIV by ex vivo infection and i.v. reinfusion of autologous cells. After each inoculation, plasma viral loads peaked between 1 and 2.5 days and then declined exponentially in one or two phases to below detection limits within 2 weeks. Although higher levels of SIV-specific cytotoxic T lymphocytes and modest increases in antibody responses were observed for each animal after the second inoculation, decay rates of the infected cells were only minimally affected. Analyzing the viral load data with a mathematical model, the in vivo viral burst size averaged 4.0 × 104 and 5.5 × 104 virions per cell for the first and second inoculations, respectively, with no significant difference between the two inoculations. This estimate, in conjunction with our prior understanding of other quantitative viral and cellular parameters during SIV and HIV infection, provides critical insights into the dynamic process of viral production and its interplay with the infected host in vivo.
机译:构建仅经历一轮感染和复制的单周期猿猴免疫缺陷病毒(scSIV),以计算体内被SIV感染的细胞所产生的viron总数。通过离体感染和静脉内注射,每隔11周用scSIV接种4只Mamu-A * 01恒河猴。再注入自体细胞。每次接种后,血浆病毒载量在1到2.5天之间达到峰值,然后在一两个阶段内呈指数下降,在2周内降至检测极限以下。尽管在第二次接种后,每只动物均观察到更高水平的SIV特异性细胞毒性T淋巴细胞和适度的抗体反应增加,但感染细胞的衰变率受到的影响很小。用数学模型分析病毒载量数据,第一次和第二次接种的体内病毒爆发大小平均为每个细胞4.0×10 4 和5.5×10 4 病毒粒子,分别,两次接种之间没有显着差异。结合我们先前对SIV和HIV感染期间其他定量病毒和细胞参数的了解,该估计值对病毒产生的动态过程及其与体内感染宿主的相互作用提供了重要的见解。

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