Department of Immunology and Microbial Science IMM-6, The Scripps Research Institute, La Jolla, California, USA.
J Virol. 2012 Apr;86(8):4578-85. doi: 10.1128/JVI.06604-11. Epub 2012 Feb 15.
Several arenaviruses, chiefly Lassa virus (LASV), cause hemorrhagic fever (HF) disease in humans and pose a significant public health concern in regions where they are endemic. On the other hand, evidence indicates that the globally distributed prototypic arenavirus lymphocytic choriomeningitis virus (LCMV) is a neglected human pathogen. The phosphatidylinositol 3-kinase (PI3K)/Akt pathway participates in many cellular processes, including cell survival and differentiation, and also has been shown to play important roles in different steps of the life cycles of a variety of viruses. Here we report that the inhibition of the PI3K/Akt pathway inhibited budding and to a lesser extent RNA synthesis, but not cell entry, of LCMV. Accordingly, BEZ-235, a PI3K inhibitor currently in cancer clinical trials, inhibited LCMV multiplication in cultured cells. These findings, together with those previously reported for Junin virus (JUNV), indicate that targeting the PI3K/Akt pathway could represent a novel antiviral strategy to combat human-pathogenic arenaviruses.
几种沙粒病毒,主要是拉萨病毒(LASV),会导致人类发生出血热(HF)疾病,并且在其流行的地区对公共卫生构成重大威胁。另一方面,有证据表明,在全球范围内分布的原型沙粒病毒淋巴细胞性脉络丛脑膜炎病毒(LCMV)是一种被忽视的人类病原体。磷酸肌醇 3-激酶(PI3K)/ Akt 途径参与许多细胞过程,包括细胞存活和分化,并且已经表明在多种病毒生命周期的不同步骤中发挥重要作用。在这里,我们报告说,PI3K/Akt 途径的抑制抑制了 LCMV 的出芽,在较小程度上抑制了 RNA 合成,但不抑制细胞进入。因此,目前正在癌症临床试验中的 PI3K 抑制剂 BEZ-235 抑制了培养细胞中的 LCMV 增殖。这些发现与先前报道的胡宁病毒(JUNV)的发现一起表明,靶向 PI3K/Akt 途径可能代表一种针对人类致病性沙粒病毒的新型抗病毒策略。