Department of Biology, The Pennsylvania State University, University Park, PA 16802, USA; E-Mail:
Viruses. 2010 Dec;2(12):2663-80. doi: 10.3390/v2122663. Epub 2010 Dec 10.
CD4 decline is a hallmark of disease onset in individuals infected with Feline Immunodeficiency Virus (FIV) or Human Immunodeficiency Virus type 1 (HIV-1). Cats that are infected with a poorly replicating, apathogenic FIV (PLV) prior to exposure to a virulent FIV strain (FIVC) maintain CD4 numbers by mechanisms that are not correlated with a measurable adaptive immune response or reduction in circulating viral load. We employed population genetic approaches based on the 3' portion of the viral genome to estimate the population structure of FIVC from single and dual infected cats. In dual infected cats, FIVC effective population size was decreased during the initial viral expansion phase, and after three weeks of infection, the population declined sharply. The FIVC population recovered to pre-bottleneck levels approximately seven weeks post-FIVC infection. However, the population emerging from the bottleneck in dual infected cats was distinct based on estimates of temporal population structure and substitution profiles. The transition to transversion rate ratio (κ) increased from early to late phases in dual infected cats due primarily to a decrease in transversions whereas in single infected cats, κ declined over time. Although one clone with extensive G to A substitutions, indicative of host cytidine deaminase editing, was recovered from a dual infected cat during the bottleneck, the post bottleneck population had an overall reduction in G to A substitutions. These data are consistent with a model of PLV-induced host restriction, putatively involving host DNA editing, that alters the dynamics of FIVC throughout the course of infection leading to disease attenuation.
CD4 下降是感染猫免疫缺陷病毒 (FIV) 或人类免疫缺陷病毒 1 型 (HIV-1) 的个体疾病发作的标志。在接触毒力 FIV 株 (FIVC) 之前,感染复制能力差、无致病性 FIV (PLV) 的猫通过与可测量的适应性免疫反应或循环病毒载量降低无关的机制维持 CD4 数量。我们采用基于病毒基因组 3' 部分的群体遗传学方法,估计来自单感染和双感染猫的 FIVC 的群体结构。在双感染猫中,FIVC 有效种群大小在病毒初始扩张阶段减少,感染三周后,种群急剧下降。FIVC 种群在感染 FIVC 约七周后恢复到瓶颈前水平。然而,基于时间种群结构和替代模式的估计,双感染猫中从瓶颈中出现的 FIVC 种群是不同的。双感染猫中,转换到颠换的比率 (κ) 在双感染猫中从早期到晚期增加,主要是由于颠换减少,而在单感染猫中,κ 随时间下降。尽管从瓶颈期的一只双感染猫中恢复了一个具有广泛 G 到 A 取代的克隆,表明宿主胞嘧啶脱氨酶编辑,但瓶颈后种群的总体 G 到 A 取代减少。这些数据与 PLV 诱导的宿主限制模型一致,推测涉及宿主 DNA 编辑,该模型改变了 FIVC 在整个感染过程中的动态,导致疾病衰减。