Laboratorio de Virología, Departamento de Química Biológica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires (UBA), 1428, Buenos Aires, Argentina.
IQUIBICEN, Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET)-UBA, Ciudad Universitaria, 1428, Buenos Aires, Argentina.
Arch Virol. 2022 Mar;167(3):935-940. doi: 10.1007/s00705-022-05388-9. Epub 2022 Feb 8.
In the present study, we analyzed the modulation of p38 cell signaling by Junín virus (JUNV) and evaluated the antiviral activity of p38 inhibitors against JUNV. While JUNV induced a progressive activation of p38 throughout the infection in Vero cells, a partial downregulation of p38 phosphorylation was observed in HEK293 and HeLa cells. The compounds SB203580 and SB202190, which are selective inhibitors of p38, significantly reduced viral protein expression and viral yield in the cell lines examined, indicating that the p38 signaling pathway might be a promising antiviral target against JUNV infection.
在本研究中,我们分析了 Junín 病毒(JUNV)对 p38 细胞信号的调节作用,并评估了 p38 抑制剂对 JUNV 的抗病毒活性。虽然 JUNV 在 Vero 细胞感染过程中诱导了 p38 的渐进性激活,但在 HEK293 和 HeLa 细胞中观察到 p38 磷酸化的部分下调。p38 的选择性抑制剂 SB203580 和 SB202190 显著降低了所检测细胞系中的病毒蛋白表达和病毒产量,表明 p38 信号通路可能是针对 JUNV 感染的有前途的抗病毒靶点。