Buskiewicz Iwona A, Koenig Andreas, Huber Sally A, Budd Ralph C
Department of Pathology, Vermont Center for Immunology & Infectious Diseases, University of Vermont, Burlington, VT 05405, USA.
Future Virol. 2012 Dec;7(12):1221-1236. doi: 10.2217/fvl.12.115.
Picornaviruses are small, nonenveloped, positive-stranded RNA viruses, which cause a wide range of animal and human diseases, based on their distinct tissue and cell type tropisms. Myocarditis, poliomyelitis, hepatitis and the common cold are the most significant human illnesses caused by picornaviruses. The host response to picornaviruses is complex, and the damage to tissues occurs not only from direct viral replication within infected cells. Picornaviruses exhibit an exceptional ability to evade the early innate immune response, resulting in chronic infection and autoimmunity. This review discusses the detailed aspects of the early innate host response to picornaviruses infection mediated by RIG-I-like helicases, their adaptor, mitochondrial ant iviral signaling protein, innate immune-induced apoptosis, and the role of caspase-8 and its regulatory paralog, FLIP, in these processes.
微小核糖核酸病毒是小型、无包膜的正链RNA病毒,根据其独特的组织和细胞类型嗜性,可导致多种动物和人类疾病。心肌炎、脊髓灰质炎、肝炎和普通感冒是由微小核糖核酸病毒引起的最严重的人类疾病。宿主对微小核糖核酸病毒的反应很复杂,组织损伤不仅源于受感染细胞内的病毒直接复制。微小核糖核酸病毒具有非凡的能力来逃避早期先天免疫反应,从而导致慢性感染和自身免疫。本综述讨论了由视黄酸诱导基因I样解旋酶介导的宿主对微小核糖核酸病毒感染的早期先天反应的详细方面、其衔接蛋白、线粒体抗病毒信号蛋白、先天免疫诱导的细胞凋亡,以及半胱天冬酶-8及其调节旁系同源物FLIP在这些过程中的作用。