Escaffre Olivier, Halliday Hailey, Borisevich Viktoriya, Casola Antonella, Rockx Barry
Department of Pathology, University of Texas Medical Branch, Galveston, TX, USA.
Department of Pediatrics, University of Texas Medical Branch, Galveston, TX, USA.
J Gen Virol. 2015 Oct;96(10):2961-2970. doi: 10.1099/jgv.0.000243. Epub 2015 Jul 14.
Nipah virus (NiV) is a zoonotic emerging pathogen that can cause severe and often fatal respiratory disease in humans. The pathogenesis of NiV infection of the human respiratory tract remains unknown. Reactive oxygen species (ROS) produced by airway epithelial cells in response to viral infections contribute to lung injury by inducing inflammation and oxidative stress; however, the role of ROS in NiV-induced respiratory disease is unknown. To investigate whether NiV induces oxidative stress in human respiratory epithelial cells, we used oxidative stress markers and monitored antioxidant gene expression. We also used ROS scavengers to assess their role in immune response modulation. Oxidative stress was confirmed in infected cells and correlated with the reduction in antioxidant enzyme gene expression. Infected cells treated by ROS scavengers resulted in a significant decrease of the (F2)-8-isoprostane marker, inflammatory responses and virus replication. In conclusion, ROS are induced during NiV infection in human respiratory epithelium and contribute to the inflammatory response. Understanding how oxidative stress contributes to NiV pathogenesis is crucial for therapeutic development.
尼帕病毒(NiV)是一种人畜共患的新兴病原体,可导致人类严重且往往致命的呼吸道疾病。NiV感染人类呼吸道的发病机制尚不清楚。气道上皮细胞在病毒感染时产生的活性氧(ROS)通过诱导炎症和氧化应激导致肺损伤;然而,ROS在NiV诱导的呼吸道疾病中的作用尚不清楚。为了研究NiV是否会在人呼吸道上皮细胞中诱导氧化应激,我们使用了氧化应激标志物并监测抗氧化基因表达。我们还使用ROS清除剂来评估它们在免疫反应调节中的作用。在感染细胞中证实了氧化应激,并且与抗氧化酶基因表达的降低相关。用ROS清除剂处理感染细胞导致(F2)-8-异前列腺素标志物、炎症反应和病毒复制显著减少。总之,在人呼吸道上皮细胞感染NiV期间会诱导ROS产生,并导致炎症反应。了解氧化应激如何促成NiV发病机制对于治疗开发至关重要。