Ryman K D, Klimstra W B, Nguyen K B, Biron C A, Johnston R E
Department of Microbiology and Immunology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, USA.
J Virol. 2000 Apr;74(7):3366-78. doi: 10.1128/jvi.74.7.3366-3378.2000.
Infection of adult 129 Sv/Ev mice with consensus Sindbis virus strain TR339 is subclinical due to an inherent restriction in early virus replication and viremic dissemination. By comparing the pathogenesis of TR339 in 129 Sv/Ev mice and alpha/beta interferon receptor null (IFN-alpha/betaR(-/-)) mice, we have assessed the contribution of IFN-alpha/beta in restricting virus replication and spread and in determining cell and tissue tropism. In adult 129 Sv/Ev mice, subcutaneous inoculation with 100 PFU of TR339 led to extremely low-level virus replication and viremia, with clearance under way by 96 h postinoculation (p.i.). In striking contrast, adult IFN-alpha/betaR(-/-) mice inoculated subcutaneously with 100 PFU of TR339 succumbed to the infection within 84 h. By 24 h p.i. a high-titer serum viremia had seeded infectious virus systemically, coincident with the systemic induction of the proinflammatory cytokines interleukin-12 (IL-12) p40, IFN-gamma, tumor necrosis factor alpha, and IL-6. Replicating virus was located in macrophage-dendritic cell (DC)-like cells at 24 h p.i. in the draining lymph node and in the splenic marginal zone. By 72 h p.i. virus replication was widespread in macrophage-DC-like cells in the spleen, liver, lung, thymus, and kidney and in fibroblast-connective tissue and periosteum, with sporadic neuroinvasion. IFN-alpha/beta-mediated restriction of TR339 infection was mimicked in vitro in peritoneal exudate cells from 129 Sv/Ev versus IFN-alpha/betaR(-/-) mice. Thus, IFN-alpha/beta protects the normal adult host from viral infection by rapidly conferring an antiviral state on otherwise permissive cell types, both locally and systemically. Ablation of the IFN-alpha/beta system alters the apparent cell and tissue tropism of the virus and renders macrophage-DC-lineage cells permissive to infection.
由于早期病毒复制和病毒血症传播存在内在限制,成年129 Sv/Ev小鼠感染辛德毕斯病毒TR339株呈亚临床状态。通过比较TR339在129 Sv/Ev小鼠和α/β干扰素受体缺失(IFN-α/βR(-/-))小鼠中的发病机制,我们评估了IFN-α/β在限制病毒复制和传播以及确定细胞和组织嗜性方面的作用。在成年129 Sv/Ev小鼠中,皮下接种100 PFU的TR339导致极低水平的病毒复制和病毒血症,接种后96小时(p.i.)病毒开始清除。与之形成鲜明对比的是,皮下接种100 PFU的TR339的成年IFN-α/βR(-/-)小鼠在84小时内死于感染。接种后24小时,高滴度血清病毒血症已将感染性病毒播散至全身,同时促炎细胞因子白细胞介素-12(IL-12)p40、IFN-γ、肿瘤坏死因子α和IL-6被全身诱导。接种后24小时,复制的病毒位于引流淋巴结和脾边缘区的巨噬细胞-树突状细胞(DC)样细胞中。接种后72小时,病毒复制广泛存在于脾脏、肝脏、肺、胸腺和肾脏的巨噬细胞-DC样细胞以及成纤维细胞-结缔组织和骨膜中,并伴有散发性神经侵袭。在来自129 Sv/Ev与IFN-α/βR(-/-)小鼠的腹腔渗出细胞中,体外模拟了IFN-α/β介导的对TR339感染的限制。因此,IFN-α/β通过在局部和全身迅速赋予原本允许感染的细胞类型抗病毒状态,保护正常成年宿主免受病毒感染。IFN-α/β系统的缺失改变了病毒明显的细胞和组织嗜性,并使巨噬细胞-DC谱系细胞易于感染。