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Profound Differences in Virus Population Genetics Correspond to Protection from CD4 Decline Resulting from Feline Lentivirus Coinfection

机译:病毒种群遗传学上的深刻差异对应于对猫慢病毒合并感染导致的CD4下降的保护作用。

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摘要

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.
机译:CD4下降是感染猫免疫缺陷病毒(FIV)或1型人类免疫缺陷病毒(HIV-1)的个体疾病发作的标志。在暴露于毒性FIV株(FIVC)之前感染复制能力差,无病原性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值。我们采用了基于病毒基因组3'部分的群体遗传方法来估计来自单只和双重感染猫的FIVC的种群结构。在双重感染的猫中,FIVC有效种群数量在最初的病毒扩展阶段减小,并且在感染三周后,种群急剧下降。 FIVC感染后约7周,FIVC种群恢复到瓶颈前的水平。但是,根据对瞬时种群结构和替代特征的估计,在双重感染的猫中从瓶颈出现的种群是不同的。双重感染猫的过渡到转化率比率(κ)从早期到晚期增加,这主要是由于转化减少,而单一感染猫的κ随着时间的推移而下降。尽管在瓶颈期从双重感染的猫中回收到一个具有广泛的G到A取代的克隆,表明宿主胞苷脱氨酶编辑,但瓶颈后种群的G到A取代总体减少。这些数据与PLV诱导的宿主限制模型一致,该模型被认为涉及宿主DNA编辑,该模型在整个感染过程中改变了FIVC的动力学,导致疾病减轻。

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