State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100050, China; Department of Pharmacology, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100050, China.
Special Pathogens Program, National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Manitoba, R3E 3R2, Canada; Department of Medical Microbiology, University of Manitoba, Winnipeg, Manitoba, R3E 0J9, Canada; Key Laboratory of Jilin Province for Zoonosis Prevention and Control, Institute of Military Veterinary, Academy of Military Medical Science, Changchun, China.
Antiviral Res. 2019 Jul;167:68-77. doi: 10.1016/j.antiviral.2019.03.014. Epub 2019 Apr 4.
Lassa virus (LASV) causes Lassa hemorrhagic fever in humans and poses a significant threat to public health in West Africa. Current therapeutic treatments for Lassa fever are limited, making the development of novel countermeasures an urgent priority. In this study, we identified losmapimod, a p38 mitogen-activated protein kinase (MAPK) inhibitor, from 102 screened compounds as an inhibitor of LASV infection. Losmapimod exerted its inhibitory effect against LASV after p38 MAPK down-regulation, and, interestingly, had no effect on other arenaviruses capable of causing viral hemorrhagic fever. Mechanistic studies showed that losmapimod inhibited LASV entry by affecting the stable signal peptide (SSP)-GP2 subunit interface of the LASV glycoprotein, thereby blocking pH-dependent viral fusion. As an aryl heteroaryl bis-carboxyamide derivative, losmapimod represents a novel chemical scaffold with anti-LASV activity, and it provides a new lead structure for the future development of LASV fusion inhibitors.
拉沙病毒(LASV)可引起人类拉沙热,对西非的公共卫生构成重大威胁。目前针对拉沙热的治疗方法有限,因此开发新的对策迫在眉睫。在这项研究中,我们从 102 种筛选出的化合物中鉴定出了一种 p38 丝裂原活化蛋白激酶(MAPK)抑制剂,即洛司帕米,它可以抑制 LASV 感染。洛司帕米通过下调 p38 MAPK 发挥对 LASV 的抑制作用,而且有趣的是,它对其他能够引起病毒性出血热的沙粒病毒没有影响。机制研究表明,洛司帕米通过影响 LASV 糖蛋白的稳定信号肽(SSP)-GP2 亚单位界面来抑制 LASV 进入,从而阻断 pH 依赖性病毒融合。作为一种芳基杂芳基双羧酰胺衍生物,洛司帕米具有抗 LASV 活性,为未来开发 LASV 融合抑制剂提供了新的先导结构。