Liedmann Swantje, Hrincius Eike R, Guy Cliff, Anhlan Darisuren, Dierkes Rüdiger, Carter Robert, Wu Gang, Staeheli Peter, Green Douglas R, Wolff Thorsten, McCullers Jonathan A, Ludwig Stephan, Ehrhardt Christina
Institute of Molecular Virology (IMV), Center for Molecular Biology of Inflammation (ZMBE), University of Muenster, Von-Esmarch-Street 56, D-48149 Muenster, Germany.
Department of Infectious Diseases, St. Jude Children's Research Hospital, 262 Danny Thomas Place, Memphis, Tennessee 38105-3678, USA.
Nat Commun. 2014 Dec 9;5:5645. doi: 10.1038/ncomms6645.
The type I interferon (IFN) response represents the first line of defence to invading pathogens. Internalized viral ribonucleoproteins (vRNPs) of negative-strand RNA viruses induce an early IFN response by interacting with retinoic acid inducible gene I (RIG-I) and its recruitment to mitochondria. Here we employ three-dimensional stochastic optical reconstruction microscopy (STORM) to visualize incoming influenza A virus (IAV) vRNPs as helical-like structures associated with mitochondria. Unexpectedly, an early IFN induction in response to vRNPs is not detected. A distinct amino-acid motif in the viral polymerases, PB1/PA, suppresses early IFN induction. Mutation of this motif leads to reduced pathogenicity in vivo, whereas restoration increases it. Evolutionary dynamics in these sequences suggest that completion of the motif, combined with viral reassortment can contribute to pandemic risks. In summary, inhibition of the immediate anti-viral response is 'pre-packaged' in IAV in the sequences of vRNP-associated polymerase proteins.
I型干扰素(IFN)反应是抵御入侵病原体的第一道防线。负链RNA病毒的内化病毒核糖核蛋白(vRNP)通过与视黄酸诱导基因I(RIG-I)相互作用并将其募集到线粒体来诱导早期IFN反应。在这里,我们采用三维随机光学重建显微镜(STORM)将传入的甲型流感病毒(IAV)vRNP可视化为与线粒体相关的螺旋状结构。出乎意料的是,未检测到针对vRNP的早期IFN诱导。病毒聚合酶PB1/PA中一个独特的氨基酸基序抑制早期IFN诱导。该基序的突变导致体内致病性降低,而恢复则增加致病性。这些序列中的进化动态表明,该基序的完成与病毒重配相结合可能会导致大流行风险。总之,IAV中vRNP相关聚合酶蛋白序列中“预先包装”了对即时抗病毒反应的抑制。