Desrosiers R C, Lifson J D, Gibbs J S, Czajak S C, Howe A Y, Arthur L O, Johnson R P
New England Regional Primate Research Center, Harvard Medical School, Southborough, Massachusetts 01772-9102, USA.
J Virol. 1998 Feb;72(2):1431-7. doi: 10.1128/JVI.72.2.1431-1437.1998.
Deletion mutants of the pathogenic clone of simian immunodeficiency virus isolate 239 (SIVmac239) were derived that are missing nef, vpr, and upstream sequences (US) in the U3 region of the LTR (SIVmac239 delta3), nef, vpx, and US (SIVmac239 delta3x), and nef, vpr, vpx, and US (SIVmac239 delta4). These multiply deleted derivatives replicated well in the continuously growing CEMx174 cell line and were infectious for rhesus monkeys. However, on the basis of virus load measurements, strength of antibody responses, and lack of disease progression, these mutants were highly attenuated. Measurements of cell-associated viral load agreed well with assays of plasma viral RNA load and with the strengths of the antibody responses; thus, these measurements likely reflected the extent of viral replication in vivo. A derivative of SIVmac239 lacking vif sequences (SIVmac239 delta vif) could be consistently grown only in a vif-complementing cell line. This delta vif virus appeared to be very weakly infectious for rhesus monkeys on the basis of sensitive antibody tests only. The weak antibody responses elicited by SIVmac239 delta vif were apparently in response to low levels of replicating virus since they were not elicited by heat-inactivated virus and the anti-SIV antibody responses persisted for greater than 1 year. These results, and the results of previous studies, allow a rank ordering of the relative virulence of nine mutant strains of SIVmac according to the following order: delta vpr > delta vpx > delta vpr delta vpx approximately delta nef > delta3 > delta3x > or = delta4 > delta vif > delta5. The results also demonstrate that almost any desired level of attenuation can be achieved, ranging from still pathogenic in a significant proportion of animals (delta vpr and delta vpx) to not detectably infectious (delta5), simply by varying the number and location of deletions in these five loci.
猿猴免疫缺陷病毒分离株239(SIVmac239)致病克隆的缺失突变体被构建出来,包括在长末端重复序列(LTR)的U3区域缺失nef、vpr和上游序列(US)的突变体(SIVmac239 delta3)、缺失nef、vpx和US的突变体(SIVmac239 delta3x)以及缺失nef、vpr、vpx和US的突变体(SIVmac239 delta4)。这些多重缺失的衍生物在持续生长的CEMx174细胞系中复制良好,并且对恒河猴具有感染性。然而,基于病毒载量测量、抗体反应强度以及疾病进展情况,这些突变体的毒力显著减弱。细胞相关病毒载量的测量结果与血浆病毒RNA载量测定以及抗体反应强度结果高度一致;因此,这些测量结果很可能反映了体内病毒复制的程度。缺失vif序列的SIVmac239衍生物(SIVmac239 delta vif)只能在一个能补充vif的细胞系中持续生长。仅基于灵敏的抗体检测,这种delta vif病毒对恒河猴的感染性似乎非常弱。SIVmac239 delta vif引发的微弱抗体反应显然是对低水平复制病毒的反应,因为热灭活病毒不会引发这种反应,并且抗SIV抗体反应持续超过1年。这些结果以及先前研究的结果,使得可以根据以下顺序对九种SIVmac突变株的相对毒力进行排序:delta vpr > delta vpx > delta vpr delta vpx ≈ delta nef > delta3 > delta3x > 或 = delta4 > delta vif > delta5。结果还表明,几乎可以通过改变这五个基因座中的缺失数量和位置,实现从在相当比例的动物中仍具致病性(delta vpr和delta vpx)到无法检测到感染性(delta5)的几乎任何所需程度的减毒。