Institute of Virology, Medical Center - University of Freiburg, Freiburg, Germany.
Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Nucleic Acids Res. 2023 Jul 7;51(12):6479-6494. doi: 10.1093/nar/gkad442.
A fundamental step in the influenza A virus (IAV) replication cycle is the coordinated packaging of eight distinct genomic RNA segments (i.e. vRNAs) into a viral particle. Although this process is thought to be controlled by specific vRNA-vRNA interactions between the genome segments, few functional interactions have been validated. Recently, a large number of potentially functional vRNA-vRNA interactions have been detected in purified virions using the RNA interactome capture method SPLASH. However, their functional significance in coordinated genome packaging remains largely unclear. Here, we show by systematic mutational analysis that mutant A/SC35M (H7N7) viruses lacking several prominent SPLASH-identified vRNA-vRNA interactions involving the HA segment package the eight genome segments as efficiently as the wild-type virus. We therefore propose that the vRNA-vRNA interactions identified by SPLASH in IAV particles are not necessarily critical for the genome packaging process, leaving the underlying molecular mechanism elusive.
流感病毒(IAV)复制周期的一个基本步骤是将八个不同的基因组 RNA 片段(即 vRNA)协调包装到病毒颗粒中。尽管该过程被认为是由基因组片段之间的特定 vRNA-vRNA 相互作用控制的,但很少有功能相互作用得到验证。最近,使用 RNA 互作组捕获方法 SPLASH 在纯化的病毒粒子中检测到大量潜在的功能 vRNA-vRNA 相互作用。然而,它们在协调基因组包装中的功能意义在很大程度上仍不清楚。在这里,我们通过系统的突变分析表明,缺失几个涉及 HA 片段的 SPLASH 鉴定的 vRNA-vRNA 相互作用的突变型 A/SC35M(H7N7)病毒能够像野生型病毒一样有效地包装八个基因组片段。因此,我们提出 SPLASH 在 IAV 粒子中鉴定的 vRNA-vRNA 相互作用不一定对基因组包装过程至关重要,这使得潜在的分子机制难以捉摸。