LeBouder Fanny, Morello Eric, Rimmelzwaan Guus F, Bosse Françoise, Péchoux Christine, Delmas Bernard, Riteau Béatrice
Unité de Virologie et Immunologie Moléculaires, UR 892 INRA, Domaine de Vilvert, 78352 Jouy-en-Josas, France.
J Virol. 2008 Jul;82(14):6820-8. doi: 10.1128/JVI.00246-08. Epub 2008 Apr 30.
For influenza viruses to become infectious, the proteolytic cleavage of hemagglutinin (HA) is essential. This usually is mediated by trypsin-like proteases in the respiratory tract. The binding of plasminogen to influenza virus A/WSN/33 leads to the cleavage of HA, a feature determining its pathogenicity and neurotropism in mice. Here, we demonstrate that plasminogen also promotes the replication of other influenza virus strains. The inhibition of the conversion of plasminogen into plasmin blocked influenza virus replication. Evidence is provided that the activation of plasminogen is mediated by the host cellular protein annexin II, which is incorporated into the virus particles. Indeed, the inhibition of plasminogen binding to annexin II by using a competitive inhibitor inhibits plasminogen activation into plasmin. Collectively, these results indicate that the annexin II-mediated activation of plasminogen supports the replication of influenza viruses, which may contribute to their pathogenicity.
流感病毒要具有传染性,血凝素(HA)的蛋白水解切割至关重要。这通常由呼吸道中的类胰蛋白酶介导。纤溶酶原与甲型流感病毒A/WSN/33的结合导致HA的切割,这一特征决定了其在小鼠中的致病性和嗜神经性。在此,我们证明纤溶酶原也促进其他流感病毒株的复制。抑制纤溶酶原向纤溶酶的转化可阻断流感病毒复制。有证据表明纤溶酶原的激活由宿主细胞蛋白膜联蛋白II介导,该蛋白被整合到病毒颗粒中。实际上,使用竞争性抑制剂抑制纤溶酶原与膜联蛋白II的结合可抑制纤溶酶原激活为纤溶酶。总体而言,这些结果表明膜联蛋白II介导的纤溶酶原激活支持流感病毒的复制,这可能有助于其致病性。