Sequential disruption of SPLASH-identified vRNA–vRNA interactions challenges their role in influenza A virus genome packaging

Author:

Jakob Celia12,Lovate Gabriel L3,Desirò Daniel4ORCID,Gießler Lara1,Smyth Redmond P56ORCID,Marquet Roland7ORCID,Lamkiewicz Kevin389ORCID,Marz Manja38910,Schwemmle Martin12ORCID,Bolte Hardin12ORCID

Affiliation:

1. Institute of Virology, Medical Center – University of Freiburg , Freiburg , Germany

2. Faculty of Medicine, University of Freiburg , Freiburg , Germany

3. RNA Bioinformatics and High-Throughput Analysis, Faculty of Mathematics and Computer Science, Friedrich Schiller University Jena , Germany

4. Department of Biochemistry, University of Cambridge , Cambridge CB2 1QW , UK

5. Helmholtz Institute for RNA-based Infection Research, Helmholtz Centre for Infection Research , Würzburg , Germany

6. Julius-Maximilians-Universität Würzburg, Faculty of Medicine , Würzburg , Germany

7. Architecture et Réactivité de l’ARN, Université de Strasbourg, CNRS, IBMC , Strasbourg , France

8. German Center for Integrative Biodiversity Research (iDiv) , Halle-Jena-Leipzig , Germany

9. European Virus Bioinformatics Center (EVBC) , Jena , Germany

10. FLI Leibniz Institute for Age Research , Jena , Germany

Abstract

Abstract 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.

Funder

FluCode Project

French National Research Agency

German Research Foundation

DFG

European Union's Horizon 2020

Marie Skłodowska-Curie Actions Innovative Training Networks

Helmholtz Association Young Investigator Group

Publisher

Oxford University Press (OUP)

Subject

Genetics

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