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马传染性贫血病毒长末端重复序列在长期隐性感染携带小马不同储存组织中的变异性及分区特征分析

Characterization of EIAV LTR variability and compartmentalization in various reservoir tissues of long-term inapparent carrier ponies.

作者信息

Reis Jenner K P, Craigo Jodi K, Cook Sheila J, Issel Charles J, Montelaro Ronald C

机构信息

Department of Molecular Genetics and Biochemistry, School of Medicine, University of Pittsburgh, Pittsburgh, PA 15261, USA.

出版信息

Virology. 2003 Jun 20;311(1):169-80. doi: 10.1016/s0042-6822(03)00168-5.

Abstract

Dynamic genomic variation resulting in changes in envelope antigenicity has been established as a fundamental mechanism of persistence by equine infectious anemia virus (EIAV), as observed with other lentiviruses, including HIV-1. In addition to the reported changes in envelope sequences, however, certain studies indicate the viral LTR as a second variable EIAV gene, with the enhancer region being designated as hypervariable. These observations have lead to the suggestion that LTR variation may alter viral replication properties to optimize to the microenvironment of particular tissue reservoirs. To test this hypothesis directly, we examined the population of LTR quasispecies contained in various tissues of two inapparent carrier ponies experimentally infected with a reference EIAV biological clone for 18 months. The results of these studies demonstrated that the EIAV LTR is in fact highly conserved with respect to the infecting LTR species after 1.5 years of persistent infection and regardless of the tissue reservoir. Thus, these comprehensive analyses demonstrate for the first time that the EIAV LTR is highly conserved during long-term persistent infection and that the observed variations in viral LTR are associated more with in vitro adaptation to replication in cultured cells rather than in vivo replication in natural target cells.

摘要

与其他慢病毒(包括HIV-1)一样,马传染性贫血病毒(EIAV)导致包膜抗原性变化的动态基因组变异已被确认为病毒持续存在的基本机制。然而,除了已报道的包膜序列变化外,某些研究表明病毒长末端重复序列(LTR)是EIAV的第二个可变基因,其增强子区域被指定为高变区。这些观察结果提示,LTR变异可能会改变病毒复制特性,以优化适应特定组织储存库的微环境。为了直接验证这一假设,我们检测了两匹经实验感染参考EIAV生物克隆18个月的无症状携带小马的各种组织中所含的LTR准种群体。这些研究结果表明,在持续感染1.5年后,无论组织储存库如何,EIAV LTR相对于感染的LTR种类实际上高度保守。因此,这些全面分析首次证明,EIAV LTR在长期持续感染期间高度保守,并且观察到的病毒LTR变异更多地与体外适应在培养细胞中的复制有关,而非与在天然靶细胞中的体内复制有关。

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