Perera Nilanka, Miller Joanna L, Zitzmann Nicole
Antiviral Research Unit, Oxford Glycobiology Institute, Department of Biochemistry, University of Oxford, Oxford, UK.
Department of Medicine, Faculty of Medical Sciences, University of Sri Jayewardenepura, Nugegoda, Sri Lanka.
Cell Microbiol. 2017 May;19(5). doi: 10.1111/cmi.12734. Epub 2017 Mar 8.
Symptomatic dengue virus (DENV) infections range from mild fever to severe haemorrhagic disease and death. Host-viral interactions play a significant role in deciding the fate of the infection. The unfolded protein response (UPR) is a prosurvival cellular reaction induced in response to DENV-mediated endoplasmic reticulum stress. The UPR has complex interactions with the cellular autophagy machinery, apoptosis, and innate immunity. DENV has evolved to manipulate the UPR to facilitate its replication and to evade host immunity. Our knowledge of this intertwined network of events is continuously developing. A better understanding of the UPR mediated antiviral and proviral effects will shed light on dengue disease pathogenesis and may help development of anti-DENV therapeutics. This review summarizes the role of the UPR in viral replication, autophagy, and DENV-induced inflammation to describe how a host response contributes to DENV pathogenesis.
有症状的登革病毒(DENV)感染范围从轻度发热到严重出血性疾病甚至死亡。宿主与病毒的相互作用在决定感染的转归中起重要作用。未折叠蛋白反应(UPR)是细胞因DENV介导的内质网应激而引发的一种促生存反应。UPR与细胞自噬机制、细胞凋亡及固有免疫存在复杂的相互作用。DENV已进化出操纵UPR以促进其复制并逃避宿主免疫的能力。我们对这一相互交织的事件网络的认识在不断发展。更好地理解UPR介导的抗病毒和促病毒作用将有助于阐明登革热疾病的发病机制,并可能有助于开发抗DENV疗法。本综述总结了UPR在病毒复制、自噬及DENV诱导的炎症中的作用,以描述宿主反应如何促成DENV发病机制。