Contreras Deisy, Arumugaswami Vaithilingaraja
Board of Governors Regenerative Medicine Institute, Cedars-Sinai Medical Center.
Board of Governors Regenerative Medicine Institute, Cedars-Sinai Medical Center; Department of Surgery, Cedars-Sinai Medical Center; Department of Surgery, David Geffen School of Medicine, University of California, Los Angeles;
J Vis Exp. 2016 Aug 23(114):54767. doi: 10.3791/54767.
Zika Virus (ZIKV) is an emerging pathogen that is linked to fetal developmental abnormalities such as microcephaly, eye defects, and impaired growth. ZIKV is an RNA virus of the Flaviviridae family. ZIKV is mainly transmitted by mosquitoes, but can also be spread by maternal to fetal vertical transmission as well as sexual contact. To date, there are no reliable treatment or vaccine options available to protect those infected by the virus. The development of a reproducible, effective Zika virus infectious cell culture system is critical for studying the molecular mechanisms of ZIKV replication as well as drug and vaccine development. In this regard, a protocol describing a mammalian cell-based in vitro Zika virus culture system for viral production and growth analysis is reported here. Details on the formation of plaques by Zika virus on a cell monolayer and plaque assay for measuring viral titer are presented. Viral genome replication kinetics and double-stranded RNA genome replicatory intermediates are determined. This culture platform was utilized to screen against a library of a small set of cytokines resulting in the identification of interferon-α (IFN-α), IFN-β and IFN-γ as potent inhibitors of Zika viral growth. In summary, an in vitro infectious Zika viral culture system and various virological assays are demonstrated in this study, which has the potential to greatly benefit the research community in elucidating further the mechanisms of viral pathogenesis and the evolution of viral virulence. Antiviral IFN-alpha can further be evaluated as a prophylactic, post-exposure prophylactic, and treatment option for Zika virus infections in high-risk populations, including infected pregnant women.
寨卡病毒(ZIKV)是一种新出现的病原体,与胎儿发育异常有关,如小头畸形、眼部缺陷和生长发育受损。寨卡病毒是黄病毒科的一种RNA病毒。寨卡病毒主要通过蚊子传播,但也可通过母婴垂直传播以及性接触传播。迄今为止,尚无可靠的治疗方法或疫苗可供保护那些感染该病毒的人。建立一种可重复、有效的寨卡病毒感染性细胞培养系统对于研究寨卡病毒复制的分子机制以及药物和疫苗开发至关重要。在这方面,本文报道了一种描述用于病毒生产和生长分析的基于哺乳动物细胞的体外寨卡病毒培养系统的方案。介绍了寨卡病毒在细胞单层上形成噬斑的细节以及用于测量病毒滴度的噬斑测定法。测定了病毒基因组复制动力学和双链RNA基因组复制中间体。利用该培养平台对一小部分细胞因子文库进行筛选,结果鉴定出干扰素-α(IFN-α)、干扰素-β和干扰素-γ是寨卡病毒生长的有效抑制剂。总之,本研究展示了一种体外感染性寨卡病毒培养系统和各种病毒学检测方法,这有可能极大地造福研究界,进一步阐明病毒致病机制和病毒毒力的演变。抗病毒干扰素-α可进一步作为高危人群(包括感染孕妇)寨卡病毒感染的预防、暴露后预防和治疗选择进行评估。