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Determination of virus burst size in vivo using a single-cycle SIV in rhesus macaques
被引:116
作者:
Chen, Hannah Yuan
Di Mascio, Michele
Perelson, Alan S.
Ho, David D.
Zhang, Linqi
机构:
[1] Rockefeller Univ, Aaron Diamond AIDS Res Ctr, New York, NY 10016 USA
[2] NIAID, NIH, Bethesda, MD 20892 USA
[3] Los Alamos Natl Lab, Div Theoret, Los Alamos, NM 87545 USA
[4] Chinese Acad Med Sci, Inst Pathogen Biol, AIDS Res Ctr, Beijing 100730, Peoples R China
[5] Tsinghua Univ, Peking Union Med Coll, Beijing 100730, Peoples R China
来源:
关键词:
dynamic;
HIV;
highly active antiretroviral therapy;
half-life;
modeling;
D O I:
10.1073/pnas.0707449104
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
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 x 10(4) and 5.5 x 10(4) 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.
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页码:19079 / 19084
页数:6
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