Guinea R, Carrasco L
Centro de Biologia Molecular, Universidad Autónoma de Madrid, Canto Blanco, Spain.
FEBS Lett. 1994 Aug 8;349(3):327-30. doi: 10.1016/0014-5793(94)00695-4.
The selective inhibitor of the vacuolar proton-ATPase, concanamycin A, powerfully blocks influenza virus entry into cells, if present during the initial times of virus infection. Attachment of virus particles to cells is not prevented by concanamycin A, rather the exit of influenza virus from endosomes is the step blocked by this macrolide antibiotic. Inhibition of influenza virus entry into cells by concanamycin A or by nigericin takes place under acidic conditions. Moreover, if the pH gradient is abolished by pre-incubation of cells in acidic pH, influenza virus entry does not occur even in the absence of any inhibitors. These results indicate that acidic conditions per se are not sufficient to promote virus entry into cells; rather this step of virus infection requires a pH gradient.
液泡质子 - ATP酶的选择性抑制剂—— concanamycin A,如果在病毒感染初期存在,能有力地阻止流感病毒进入细胞。Concanamycin A 不会阻止病毒颗粒与细胞的附着,而是这种大环内酯类抗生素会阻断流感病毒从内体中释放出来这一步骤。Concanamycin A 或尼日利亚菌素在酸性条件下会抑制流感病毒进入细胞。此外,如果通过在酸性pH条件下预孵育细胞来消除pH梯度,即使没有任何抑制剂,流感病毒也不会进入细胞。这些结果表明,酸性条件本身不足以促进病毒进入细胞;相反,病毒感染的这一步骤需要pH梯度。