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Efficient Replication Of Rhesus Cytomegalovirus Variants In Multiple Rhesus And Human Cell Types

机译:恒河猴巨细胞病毒变种在多种恒河猴和人类细胞类型中的高效复制

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Rhesus cytomegalovirus infection of rhesus macaques has emerged as a model for human cytomegalovirus pathogenesis. The UL128-UL131 locus of the human virus is a primary determinant for viral entry into epithelial cells, an important cell type during cytomegalovirus infection. Rhesus cytomegalovirus strain 68-1 spreads slowly when grown in cultured rhesus epithelial cells, and it does not code for ORFs corresponding to UL128 and the second exon of UL130. We repaired the UL128-UL131 locus of strain 68-1, using rhesus cytomegalovirus strain 180.92 as template, to generate BRh68-1.1. We also repaired a mutation in the UL36 ORF in BRh68-1.1 to make BRh68-1.2. Both repaired derivatives replicate much more efficiently than parental 68-1 virus in rhesus epithelial cells, suggesting that strain 68-1 may be attenuated. Intriguingly, BRh68-1.1 and BRh68-1.2 replicate efficiently in cultured human epithelial cells and endothelial cells. The extended human cell host range of the repaired viruses raises the possibility that rhesus cytomegalovirus-like viruses will be found in humans.
机译:恒河猴猕猴的巨细胞病毒感染已经成为人类巨细胞病毒发病机理的模型。人病毒的UL128-UL131基因座是病毒进入上皮细胞(在巨细胞病毒感染期间的一种重要细胞类型)的主要决定因素。当在培养的恒河猴上皮细胞中生长时,恒河猴巨细胞病毒株68-1传播缓慢,并且它不编码对应于UL128和UL130第二外显子的ORF。我们使用恒河猴巨细胞病毒菌株180.92作为模板修复了菌株68-1的UL128-UL131基因座,以生成BRh68-1.1。我们还修复了BRh68-1.1中UL36 ORF中的一个突变,使其成为BRh68-1.2。在恒河猴上皮细胞中,两种修复的衍生物比亲本68-1病毒复制效率更高,这表明68-1株可能被减毒。有趣的是,BRh68-1.1和BRh68-1.2在培养的人上皮细胞和内皮细胞中有效复制。修复病毒的人类细胞宿主范围扩大,增加了在人体内发现恒河猴巨细胞病毒样病毒的可能性。

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