Center for Vaccine Research, University of Pittsburgh, Pittsburgh, PA, USA; University of Pittsburgh Graduate School of Public Health, Pittsburgh, PA, USA.
Center for Vaccine Research, University of Pittsburgh, Pittsburgh, PA, USA; Department of Immunology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Virology. 2019 Jan 2;526:173-179. doi: 10.1016/j.virol.2018.10.021. Epub 2018 Nov 2.
Rift Valley fever virus (RVFV) is a zoonotic disease of livestock that causes several clinical outcomes in people including febrile disease, hemorrhagic fever, and/or encephalitis. After aerosol infection with RVFV, Lewis rats develop lethal encephalitic disease, and we use this as a model for studying disease mechanisms of RVFV infection in the brain. Permeability of the brain vasculature in relation to virus invasion and replication is not known. Here, we found that vascular permeability in the brain occurred late in the course of infection and corresponded temporally to expression of matrix metalloproteinase-9 (MMP-9). Virus replication was ongoing within the central nervous system for several days prior to detectable vascular leakage. Based on this study, vascular permeability was not required for entry of RVFV into the brain of rats. Prevention of vascular leakage late in infection may be an important component for prevention of lethal neurological disease in the rat model.
裂谷热病毒(RVFV)是一种家畜的人畜共患病,可导致人类出现多种临床结果,包括发热、出血热和/或脑炎。经 RVFV 气溶胶感染后,刘易斯大鼠会发展为致命性脑炎,我们将其用作研究 RVFV 感染大脑的疾病机制的模型。病毒入侵和复制与脑血管通透性的关系尚不清楚。在这里,我们发现脑血管通透性在感染过程后期发生,与基质金属蛋白酶 9(MMP-9)的表达具有时间相关性。病毒复制在中枢神经系统内持续数天,之后才出现可检测到的血管渗漏。基于这项研究,RVFV 进入大鼠大脑并不需要血管通透性。在感染后期预防血管渗漏可能是预防大鼠模型中致命性神经疾病的一个重要组成部分。