Lilja Anders E, Chang W L William, Barry Peter A, Becerra S Patricia, Shenk Thomas E
Department of Molecular Biology, Lewis Thomas Laboratory, Princeton University, Princeton, NJ 08544, USA.
J Virol. 2008 Mar;82(5):2170-81. doi: 10.1128/JVI.02316-07. Epub 2007 Dec 19.
Rhesus cytomegalovirus (RhCMV) is an emerging model for human cytomegalovirus (HCMV) pathogenesis that facilitates experimental CMV infection of a natural primate host closely related to humans. We have generated a library of RhCMV mutants with lesions in genes whose HCMV orthologues have been characterized as nonessential for replication in human fibroblasts, and we characterized their replication in rhesus fibroblasts and epithelial cells. The RhCMV mutants grew well in fibroblasts, as predicted by earlier studies with HCMV. However, mutations in four genes caused replication defects in rhesus retinal pigment epithelial cells: Rh01 (an HCMV TRL1 orthologue), Rh159 (HCMV UL148), Rh160 (HCMV UL132), and Rh203 (HCMV US22). Growth of the Rh01-deficient mutant was examined in detail. After entry into epithelial cells, the mutant expressed representative viral proteins, accumulated viral DNA, and generated infectious virus, but it failed to spread efficiently. We conclude that Rh01 is a cell tropism determinant that has the potential to dramatically affect virus spread and pathogenesis.
恒河猴巨细胞病毒(RhCMV)是人类巨细胞病毒(HCMV)发病机制研究中新兴的一种模型,它有助于在与人类密切相关的天然灵长类宿主中进行实验性CMV感染。我们构建了一个RhCMV突变体文库,这些突变体的基因发生了损伤,其HCMV同源基因已被证明对在人成纤维细胞中复制并非必需,并且我们对它们在恒河猴成纤维细胞和上皮细胞中的复制情况进行了表征。正如早期对HCMV的研究所预测的那样,RhCMV突变体在成纤维细胞中生长良好。然而,四个基因的突变导致其在恒河猴视网膜色素上皮细胞中出现复制缺陷:Rh01(HCMV TRL1的同源物)、Rh159(HCMV UL148)、Rh160(HCMV UL132)和Rh203(HCMV US22)。我们对Rh01缺陷型突变体的生长情况进行了详细研究。该突变体进入上皮细胞后,能够表达代表性的病毒蛋白,积累病毒DNA,并产生有感染性的病毒,但它无法有效地传播。我们得出结论,Rh01是一种细胞嗜性决定因素,有可能显著影响病毒的传播和发病机制。