Mlera Luwanika, Melik Wessam, Bloom Marshall E
Rocky Mountain Laboratories, Laboratory of Virology, National Institutes of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT, USA.
Pathog Dis. 2014 Jul;71(2):137-63. doi: 10.1111/2049-632X.12178. Epub 2014 May 12.
In nature, vector-borne flaviviruses are persistently cycled between either the tick or mosquito vector and small mammals such as rodents, skunks, and swine. These viruses account for considerable human morbidity and mortality worldwide. Increasing and substantial evidence of viral persistence in humans, which includes the isolation of RNA by RT-PCR and infectious virus by culture, continues to be reported. Viral persistence can also be established in vitro in various human, animal, arachnid, and insect cell lines in culture. Although some research has focused on the potential roles of defective virus particles, evasion of the immune response through the manipulation of autophagy and/or apoptosis, the precise mechanism of flavivirus persistence is still not well understood. We propose additional research for further understanding of how viral persistence is established in different systems. Avenues for additional studies include determining whether the multifunctional flavivirus protein NS5 has a role in viral persistence, the development of relevant animal models of viral persistence, and investigating the host responses that allow vector-borne flavivirus replication without detrimental effects on infected cells. Such studies might shed more light on the viral-host relationships and could be used to unravel the mechanisms for establishment of persistence.
在自然界中,虫媒传播的黄病毒在蜱或蚊子媒介与小型哺乳动物(如啮齿动物、臭鼬和猪)之间持续循环。这些病毒在全球范围内导致了相当多的人类发病和死亡。不断有大量证据表明病毒在人类中持续存在,包括通过逆转录聚合酶链反应(RT-PCR)分离RNA以及通过培养分离出感染性病毒。病毒持续性也可以在体外培养的各种人类、动物、蛛形纲动物和昆虫细胞系中建立。尽管一些研究集中在缺陷病毒颗粒的潜在作用、通过操纵自噬和/或凋亡来逃避免疫反应,但黄病毒持续性的确切机制仍未得到充分理解。我们建议进行更多研究,以进一步了解病毒在不同系统中如何建立持续性。更多研究的途径包括确定多功能黄病毒蛋白NS5是否在病毒持续性中起作用、开发相关的病毒持续性动物模型,以及研究允许虫媒传播的黄病毒复制而不对感染细胞产生有害影响的宿主反应。此类研究可能会更深入地揭示病毒与宿主的关系,并可用于阐明建立持续性的机制。