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猫免疫缺陷病毒感染无症状期的外周免疫表型和病毒启动子变异。

Peripheral immunophenotype and viral promoter variants during the asymptomatic phase of feline immunodeficiency virus infection.

机构信息

Department of Pathology, Microbiology and Immunology, School of Veterinary Medicine, University California, Davis, 4206 Vet Med 3A, Davis, CA 95616, USA.

Department of Pathology, Microbiology and Immunology, School of Veterinary Medicine, University California, Davis, 4206 Vet Med 3A, Davis, CA 95616, USA.

出版信息

Virus Res. 2014 Jan 22;179:34-43. doi: 10.1016/j.virusres.2013.11.017. Epub 2013 Nov 28.

Abstract

Feline immunodeficiency virus (FIV)-infected cats enter a clinically asymptomatic phase during chronic infection. Despite the lack of overt clinical disease, the asymptomatic phase is characterized by persistent immunologic impairment. In the peripheral blood obtained from cats experimentally infected with FIV-C for approximately 5 years, we identified a persistent inversion of the CD4/CD8 ratio. We cloned and sequenced the FIV-C long terminal repeat containing the viral promoter from cells infected with the inoculating virus and from in vivo-derived peripheral blood mononuclear cells and CD4 T cells isolated at multiple time points throughout the asymptomatic phase. Relative to the inoculating virus, viral sequences amplified from cells isolated from all of the infected animals demonstrated multiple single nucleotide mutations and a short deletion within the viral U3, R and U5 regions. A transcriptionally inactivating proviral mutation in the U3 promoter AP-1 site was identified at multiple time points from all of the infected animals but not within cell-associated viral RNA. In contrast, no mutations were identified within the sequence of the viral dUTPase gene amplified from PBMC isolated at approximately 5 years post-infection relative to the inoculating sequence. The possible implications of these mutations to viral pathogenesis are discussed.

摘要

猫免疫缺陷病毒(FIV)感染的猫在慢性感染期间进入临床无症状阶段。尽管没有明显的临床疾病,但无症状阶段的特征是持续的免疫功能障碍。在从大约感染 FIV-C 5 年的猫中获得的外周血中,我们发现 CD4/CD8 比值持续倒置。我们从感染接种病毒的细胞和从无症状期多个时间点分离的体内衍生的外周血单核细胞和 CD4 T 细胞中克隆和测序了包含病毒启动子的 FIV-C 长末端重复序列。与接种病毒相比,从所有感染动物分离的细胞中扩增的病毒序列显示出多个单核苷酸突变和病毒 U3、R 和 U5 区域内的短缺失。在所有感染动物的多个时间点均发现了 U3 启动子 AP-1 位点的转录失活前病毒突变,但在细胞相关的病毒 RNA 中未发现突变。相比之下,从感染后约 5 年分离的 PBMC 中扩增的病毒 dUTPase 基因序列与接种序列相比,未发现任何突变。讨论了这些突变对病毒发病机制的可能影响。

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