Abstract

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.

Highlights

  • IntroductionThe influenza A virus (IAV) genome comprises eight individual ribonucleoprotein (RNP)

  • The influenza A virus (IAV) genome comprises eight individual ribonucleoprotein (RNP)complexes each with a single-stranded negative-sense viral RNA segment encoding one or more proteins

  • Udorn PB1 gene, we used overlapping PCR to divide the PB1 gene segment into approximate thirds and create plasmids encoding a series of chimeric PB1 genes containing sections swapped between

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Summary

Introduction

The influenza A virus (IAV) genome comprises eight individual ribonucleoprotein (RNP). Complexes each with a single-stranded negative-sense viral RNA (vRNA) segment encoding one or more proteins. In each RNP complex, the vRNA is encapsidated by nucleoprotein (NP) and the 30 and 50 termini show inverted complementarity and associate to form a double stranded structure referred to as the panhandle [1]. The termini are attached to the viral RNA-dependent. Each RNP is an independent unit for transcription and replication of the associated vRNA [4,5]. Each gene segment encodes at least one essential viral protein, complicating packaging of the viral genome, as the virus must incorporate one copy of each vRNA to be fully infectious. Single-molecule fluorescent in situ hybridization analysis directly showed that only one copy of each

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