Department of Microbiology and Immunology, University of California, San Francisco, California, USA.
Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford University, Stanford, California, USA.
J Infect Dis. 2023 Oct 18;228(Suppl 6):S427-S445. doi: 10.1093/infdis/jiac426.
Picornaviruses are nonenveloped particles with a single-stranded RNA genome of positive polarity. This virus family includes poliovirus, hepatitis A virus, rhinoviruses, and Coxsackieviruses. Picornaviruses are common human pathogens, and infection can result in a spectrum of serious illnesses, including acute flaccid myelitis, severe respiratory complications, and hand-foot-mouth disease. Despite research on poliovirus establishing many fundamental principles of RNA virus biology and the first transgenic animal model of disease for infection by a human virus, picornaviruses are understudied. Existing knowledge gaps include, identification of molecules required for virus entry, understanding cellular and humoral immune responses elicited during virus infection, and establishment of immune-competent animal models of virus pathogenesis. Such knowledge is necessary for development of pan-picornavirus countermeasures. Defining enterovirus A71 and D68, human rhinovirus C, and echoviruses 29 as prototype pathogens of this virus family may provide insight into picornavirus biology needed to establish public health strategies necessary for pandemic preparedness.
小 RNA 病毒是无包膜的颗粒,具有单链 RNA 基因组的正极性。这个病毒家族包括脊髓灰质炎病毒、甲型肝炎病毒、鼻病毒和柯萨奇病毒。小 RNA 病毒是常见的人类病原体,感染可导致一系列严重疾病,包括急性弛缓性脊髓炎、严重的呼吸道并发症和手足口病。尽管对脊髓灰质炎病毒的研究确立了 RNA 病毒生物学的许多基本原则,以及第一个用于感染人类病毒的转基因动物疾病模型,但小 RNA 病毒的研究还很不足。现有的知识空白包括鉴定病毒进入所需的分子、了解病毒感染期间诱导的细胞和体液免疫反应,以及建立病毒发病机制的免疫功能健全的动物模型。这些知识是开发泛小 RNA 病毒对策所必需的。将肠道病毒 A71 和 D68、人鼻病毒 C 和柯萨奇病毒 29 定义为该病毒家族的原型病原体,可能有助于了解小 RNA 病毒生物学,从而制定大流行准备所需的公共卫生策略。