Miller Craig, Bielefeldt-Ohmann Helle, MacMillan Martha, Huitron-Resendiz Salvador, Henriksen Steven, Elder John, VandeWoude Susan
Department of Microbiology, Immunology, and Pathology, College of Veterinary Medicine and Biomedical Sciences, Colorado State University, Fort Collins, CO 80523-1619, USA.
Vet Immunol Immunopathol. 2011 Oct 15;143(3-4):282-91. doi: 10.1016/j.vetimm.2011.06.006. Epub 2011 Jun 12.
Feline immunodeficiency virus (FIV) is a naturally occurring lentivirus of domestic cats, and is the causative agent of feline AIDS. Similar to human immunodeficiency virus (HIV), the pathogenesis of FIV involves infection of lymphocytes and macrophages, and results in chronic progressive immune system collapse and death. Neuropathologic correlates of FIV infection have not yet been elucidated, and may be relevant to understanding HIV-associated neurologic disease (neuroAIDS). As in HIV, FIV strains have been shown to express differential tendencies towards development of clinical neuroAIDS. To interrogate viral genetic determinants that might contribute to neuropathogenicity, cats were exposed to two well-characterized FIV strains with divergent clinical phenotypes and a chimeric strain as follows: FIV(PPR) (PPR, relatively apathogenic but associated with neurologic manifestations), FIV(C36) (C36, immunopathogenic but without associated neurologic disease), and Pcenv (a chimeric virus consisting of a PPR backbone with substituted C36 env region). A sham inoculum control group was also included. Peripheral nerve conduction velocity, CNS imaging studies, viral loads and hematologic analysis were performed over a 12 month period. At termination of the study (350 days post-inoculation), brain sections were obtained from four anatomic locations known to be involved in human and primate lentiviral neuroAIDS. Histological and immunohistochemical evaluation with seven markers of inflammation revealed that Pcenv infection resulted in mild inflammation of the CNS, microglial activation, neuronal degeneration and apoptosis, while C36 and PPR strains induced minimal neuropathologic changes. Conduction velocity aberrations were noted peripherally in all three groups at 63 weeks post-infection. Pcenv viral load in this study was intermediate to the parental strains (C36 demonstrating the highest viral load and PPR the lowest). These results collectively suggest that (i) 3' C36 genomic elements contribute to viral replication characteristics, and (ii) 5' PPR genomic elements contribute to CNS manifestations. This study illustrates the potential for FIV to provide valuable information about neuroAIDS pathogenesis related to genotype and viral kinetics, as well as to identify strains useful to evaluation of therapeutic intervention.
猫免疫缺陷病毒(FIV)是家猫自然感染的一种慢病毒,是猫艾滋病的病原体。与人类免疫缺陷病毒(HIV)相似,FIV的发病机制涉及淋巴细胞和巨噬细胞的感染,并导致慢性进行性免疫系统崩溃和死亡。FIV感染的神经病理学相关性尚未阐明,可能与理解HIV相关神经疾病(神经艾滋病)有关。与HIV一样,FIV毒株已被证明在临床神经艾滋病的发展中表现出不同的倾向。为了探究可能导致神经致病性的病毒遗传决定因素,将猫暴露于两种具有不同临床表型的特征明确的FIV毒株和一种嵌合毒株,如下所示:FIV(PPR)(PPR,相对无致病性但与神经表现相关)、FIV(C36)(C36,具有免疫致病性但无相关神经疾病)和Pcenv(一种嵌合病毒,由具有替代C36 env区域的PPR主干组成)。还包括一个假接种对照组。在12个月的时间内进行外周神经传导速度、中枢神经系统成像研究、病毒载量和血液学分析。在研究结束时(接种后第350天),从已知与人类和灵长类慢病毒神经艾滋病有关的四个解剖位置获取脑切片。用七种炎症标志物进行组织学和免疫组织化学评估发现,Pcenv感染导致中枢神经系统轻度炎症、小胶质细胞活化、神经元变性和凋亡,而C36和PPR毒株诱导的神经病理学变化最小。在感染后63周时,所有三组在外周均观察到传导速度异常。本研究中Pcenv的病毒载量介于亲本毒株之间(C36的病毒载量最高,PPR的最低)。这些结果共同表明:(i)3' C36基因组元件有助于病毒复制特征,(ii)' PPR基因组元件有助于中枢神经系统表现。本研究说明了FIV在提供有关与基因型和病毒动力学相关的神经艾滋病发病机制的有价值信息方面的潜力,以及识别对评估治疗干预有用的毒株的潜力。