Department of Microbiology, Immunology and Molecular Genetics, University of California-Los Angeles, CA 90095, USA.
Expert Rev Mol Med. 2011 Feb 24;13:e6. doi: 10.1017/S1462399410001754.
In recent years, several paramyxoviruses have emerged to infect humans, including previously unidentified zoonoses. Hendra and Nipah viruses (henipaviruses within this family) were first identified in the 1990s in Australia, Malaysia and Singapore, causing epidemics with high mortality and morbidity rates in affected animals and humans. Other paramyxoviruses, such as Menangle virus, Tioman virus, human metapneumovirus and avian paramyxovirus 1, which cause less morbidity in humans, have also been recently identified. Although the Paramyxoviridae family of viruses has been previously recognised as biomedically and veterinarily important, the recent emergence of these paramyxoviruses has focused our attention on this family. Antiviral drugs can be designed to target specific important determinants of the viral life cycle. Therefore, identifying and understanding the mechanistic underpinnings of viral entry, replication, assembly and budding will be critical in the development of antiviral therapeutic agents. This review focuses on the molecular mechanisms discovered and the antiviral strategies pursued in recent years for emerging paramyxoviruses, with particular emphasis on viral entry and exit mechanisms.
近年来,有几种副粘病毒已出现感染人类,包括先前未识别的人畜共患病。亨德拉病毒和尼帕病毒(该科内的亨尼帕病毒)于 20 世纪 90 年代在澳大利亚、马来西亚和新加坡首次被发现,导致受感染动物和人类的死亡率和发病率很高的流行。其他副粘病毒,如曼南格病毒、蒂奥曼病毒、人类偏肺病毒和禽副粘病毒 1,在人类中引起的发病率较低,最近也被发现。尽管副粘病毒科的病毒以前被认为具有重要的医学和兽医意义,但这些副粘病毒的最近出现引起了我们对该家族的关注。抗病毒药物可以设计针对病毒生命周期的特定重要决定因素。因此,鉴定和理解病毒进入、复制、组装和出芽的机制基础对于开发抗病毒治疗剂至关重要。本综述重点介绍了近年来发现的针对新兴副粘病毒的分子机制和抗病毒策略,特别强调了病毒进入和退出机制。