Baer Alan, Shafagati Nazly, Benedict Ashwini, Ammosova Tatiana, Ivanov Andrey, Hakami Ramin M, Terasaki Kaori, Makino Shinji, Nekhai Sergei, Kehn-Hall Kylene
National Center for Biodefense and Infectious Diseases, School of Systems Biology, George Mason University, Manassas, VA, USA.
Center for Sickle Cell Disease, Department of Medicine, Howard University, Washington, D.C., USA.
Antiviral Res. 2016 Mar;127:79-89. doi: 10.1016/j.antiviral.2016.01.007. Epub 2016 Jan 20.
Rift Valley fever virus (RVFV), genus Phlebovirus family Bunyaviridae, is an arthropod-borne virus endemic throughout sub-Saharan Africa. Recent outbreaks have resulted in cyclic epidemics with an increasing geographic footprint, devastating both livestock and human populations. Despite being recognized as an emerging threat, relatively little is known about the virulence mechanisms and host interactions of RVFV. To date there are no FDA approved therapeutics or vaccines for RVF and there is an urgent need for their development. The Ser/Thr protein phosphatase 1 (PP1) has previously been shown to play a significant role in the replication of several viruses. Here we demonstrate for the first time that PP1 plays a prominent role in RVFV replication early on during the viral life cycle. Both siRNA knockdown of PP1α and a novel PP1-targeting small molecule compound 1E7-03, resulted in decreased viral titers across several cell lines. Deregulation of PP1 was found to inhibit viral RNA production, potentially through the disruption of viral RNA transcript/protein interactions, and indicates a potential link between PP1α and the viral L polymerase and nucleoprotein. These results indicate that PP1 activity is important for RVFV replication early on during the viral life cycle and may prove an attractive therapeutic target.
裂谷热病毒(RVFV)属于布尼亚病毒科白蛉病毒属,是一种节肢动物传播的病毒,在撒哈拉以南非洲地区流行。最近的疫情导致周期性流行,地理范围不断扩大,对牲畜和人类种群都造成了破坏。尽管被认为是一种新出现的威胁,但人们对RVFV的毒力机制和宿主相互作用了解相对较少。迄今为止,美国食品药品监督管理局(FDA)尚未批准用于裂谷热的治疗药物或疫苗,因此迫切需要开发此类药物和疫苗。丝氨酸/苏氨酸蛋白磷酸酶1(PP1)先前已被证明在几种病毒的复制中起重要作用。在此,我们首次证明PP1在病毒生命周期早期的RVFV复制中起显著作用。PP1α的小干扰RNA(siRNA)敲低以及一种新型的靶向PP1的小分子化合物1E7-03,均导致几种细胞系中的病毒滴度降低。发现PP1失调会抑制病毒RNA的产生,可能是通过破坏病毒RNA转录本/蛋白质相互作用实现的,这表明PP1α与病毒L聚合酶和核蛋白之间存在潜在联系。这些结果表明,PP1活性在病毒生命周期早期对RVFV复制很重要,可能是一个有吸引力的治疗靶点。