United States Army Medical Research Institute of Infectious Diseases-USAMRIID, Fort Detrick, MD, USA.
Virology. 2012;431(1-2):58-70. doi: 10.1016/j.virol.2012.05.012. Epub 2012 Jun 9.
Detailed ultrastructural studies of Rift Valley fever virus (RVFV) in the mouse model are needed to develop and characterize a small animal model of RVF for the evaluation of potential vaccines and therapeutics. In this study, the ultrastructural features of RVFV infection in the mouse model were analyzed. The main changes in the liver included the presence of viral particles in hepatocytes and hepatic stem cells accompanied by hepatocyte apoptosis. However, viral particles were observed rarely in the liver; in contrast, particles were extremely abundant in the CNS. Despite extensive lymphocytolysis, direct evidence of viral replication was not observed in the lymphoid tissue. These results correlate with the acute-onset hepatitis and delayed-onset encephalitis that are dominant features of severe human RVF, but suggest that host immune-mediated mechanisms contribute significantly to pathology. The results of this study expand our knowledge of RVFV-host interactions and further characterize the mouse model of RVF.
详细的裂谷热病毒(RVFV)在小鼠模型中的超微结构研究对于开发和表征裂谷热的小动物模型以评估潜在的疫苗和疗法是必要的。在这项研究中,分析了 RVFV 感染在小鼠模型中的超微结构特征。肝脏的主要变化包括肝细胞和肝干细胞中存在病毒颗粒,伴随着肝细胞凋亡。然而,肝脏中很少观察到病毒颗粒;相反,颗粒在中枢神经系统中极为丰富。尽管淋巴细胞大量溶解,但在淋巴组织中未观察到病毒复制的直接证据。这些结果与急性发作性肝炎和迟发性脑炎相关,这是严重人类 RVF 的主要特征,但表明宿主免疫介导的机制对病理学有重要贡献。这项研究的结果扩展了我们对 RVFV-宿主相互作用的认识,并进一步描述了 RVF 的小鼠模型。