Gilbertson Brad, Zheng Tian, Gerber Marie, Printz-Schweigert Anne, Ong Chi, Marquet Roland, Isel Catherine, Rockman Steven, Brown Lorena
Department of Microbiology and Immunology, The University of Melbourne at the Peter Doherty Institute of Infection and Immunity, Parkville 3010, Victoria, Australia.
Architecture et Réactivité de l'ARN, Université de Strasbourg, CNRS, IBMC, 15 rue René Descartes, Strasbourg 67084, France.
Viruses. 2016 Aug 20;8(8):238. doi: 10.3390/v8080238.
The influenza A virus genome comprises eight negative-sense viral RNAs (vRNAs) that form individual ribonucleoprotein (RNP) complexes. In order to incorporate a complete set of each of these vRNAs, the virus uses a selective packaging mechanism that facilitates co-packaging of specific gene segments but whose molecular basis is still not fully understood. Recently, we used a competitive transfection model where plasmids encoding the A/Puerto Rico/8/34 (PR8) and A/Udorn/307/72 (Udorn) PB1 gene segments were competed to show that the Udorn PB1 gene segment is preferentially co-packaged into progeny virions with the Udorn NA gene segment. Here we created chimeric PB1 genes combining both Udorn and PR8 PB1 sequences to further define the location within the Udorn PB1 gene that drives co-segregation of these genes and show that nucleotides 1776-2070 of the PB1 gene are crucial for preferential selection. In vitro assays examining specific interactions between Udorn NA vRNA and purified vRNAs transcribed from chimeric PB1 genes also supported the importance of this region in the PB1-NA interaction. Hence, this work identifies an association between viral genes that are co-selected during packaging. It also reveals a region potentially important in the RNP-RNP interactions within the supramolecular complex that is predicted to form prior to budding to allow one of each segment to be packaged in the viral progeny. Our study lays the foundation to understand the co-selection of specific genes, which may be critical to the emergence of new viruses with pandemic potential.
甲型流感病毒基因组由八个负链病毒RNA(vRNA)组成,这些vRNA形成各自的核糖核蛋白(RNP)复合体。为了纳入这些vRNA中的每一种的完整集合,病毒使用一种选择性包装机制,该机制促进特定基因片段的共包装,但其分子基础仍未完全了解。最近,我们使用了一种竞争性转染模型,其中编码A/波多黎各/8/34(PR8)和A/乌东/307/72(乌东)PB1基因片段的质粒相互竞争,结果表明乌东PB1基因片段优先与乌东NA基因片段共包装到子代病毒颗粒中。在这里,我们创建了结合乌东和PR8 PB1序列的嵌合PB1基因,以进一步确定乌东PB1基因中驱动这些基因共分离的位置,并表明PB1基因的1776 - 2070核苷酸对于优先选择至关重要。检测乌东NA vRNA与从嵌合PB1基因转录的纯化vRNA之间特定相互作用的体外试验也支持了该区域在PB1 - NA相互作用中的重要性。因此,这项工作确定了包装过程中共同选择的病毒基因之间的关联。它还揭示了一个在超分子复合体中的RNP - RNP相互作用中可能重要的区域,预计该复合体在出芽之前形成,以使每个片段中的一个被包装到病毒子代中。我们的研究为理解特定基因的共同选择奠定了基础,这可能对具有大流行潜力的新病毒的出现至关重要。