Pandrea Ivona, Silvestri Guido, Onanga Richard, Veazey Ronald S, Marx Preston A, Hirsch Vanessa, Apetrei Cristian
Tulane National Primate Research Center, Covington, LA 70433, USA.
J Med Primatol. 2006 Aug;35(4-5):194-201. doi: 10.1111/j.1600-0684.2006.00168.x.
To define potential common features of simian immunodeficiency virus (SIV) infections in different naturally infected host species, we compared the dynamics of viral replication in 31 African green monkeys (10 sabeus, 15 vervets and seven Caribbean AGMs), 14 mandrills and three sooty mangabeys (SMs) that were experimentally infected with their species-specific viruses.
After infection, these SIVs replicated rapidly reaching viral loads (VLs) of 10(5)-10(9) copies/ml of plasma between days 9-14 post-infection (p.i). Set point viremia was established between days 42 and 60 p.i., with levels of approximately 10(5)-10(6) copies/ml in SM and mandrills, and lower levels (10(3)-10(5) copies/ml) in AGMs. VL during the chronic phase did not correlate with viral genome structure: SIVmnd-2 (a vpx-containing virus) and SIVmnd-1 (which does not contain vpu or vpx) replicated to similar levels in mandrills. VL was dependent on virus strain: vervets infected with three different viral strains showed different patterns of viral replication. The pattern of viral replication of SIVagm.sab, which uses both CCR5 and CXCR4 co-receptors was similar to those of the other viruses.
Our results show a common pattern of SIV replication in naturally and experimentally infected hosts. This is similar overall to that observed in pathogenic SIV infection of macaques. This result indicates that differences in clinical outcome between pathogenic and non-pathogenic infections rely on host responses rather than the characteristics of the virus itself.
为了确定不同自然感染宿主物种中猴免疫缺陷病毒(SIV)感染的潜在共同特征,我们比较了31只非洲绿猴(10只 sabeus、15只黑长尾猴和7只加勒比非洲绿猴)、14只山魈和3只乌黑白眉猴(SM)在实验感染其物种特异性病毒后的病毒复制动态。
感染后,这些SIV迅速复制,在感染后(p.i)第9至14天之间血浆病毒载量(VL)达到10⁵ - 1⁰⁹拷贝/毫升。在感染后第42至60天建立了稳定期病毒血症,SM和山魈中的水平约为10⁵ - 1⁰⁶拷贝/毫升,而非洲绿猴中的水平较低(10³ - 10⁵拷贝/毫升)。慢性期的VL与病毒基因组结构无关:SIVmnd - 2(一种含vpx的病毒)和SIVmnd - 1(不含vpu或vpx)在山魈中复制到相似水平。VL取决于病毒株:感染三种不同病毒株的黑长尾猴表现出不同的病毒复制模式。使用CCR5和CXCR4共受体的SIVagm.sab的病毒复制模式与其他病毒相似。
我们的结果显示了SIV在自然感染和实验感染宿主中的共同复制模式。这总体上与猕猴致病性SIV感染中观察到的模式相似。这一结果表明,致病性和非致病性感染之间临床结果的差异取决于宿主反应而非病毒本身的特征。