Abstract

A segmented genome enables influenza virus to undergo reassortment when two viruses infect the same cell. Although reassortment is involved in the creation of pandemic influenza strains and is routinely used to produce influenza vaccines, our understanding of the factors that drive the emergence of dominant gene constellations during this process is incomplete. Recently, we defined a spectrum of interactions between the gene segments of the A/Udorn/307/72 (H3N2) (Udorn) strain that occur within virus particles, a major interaction being between the NA and PB1 gene segments. In addition, we showed that the Udorn PB1 is preferentially incorporated into reassortant viruses that express the Udorn NA. Here we use an influenza vaccine seed production model where eggs are coinfected with Udorn and the high yielding A/Puerto Rico/8/34 (H1N1) (PR8) virus and track viral genotypes through the reassortment process under antibody selective pressure to determine the impact of Udorn NA-PB1 co-selection. We discovered that 86% of the reassortants contained the PB1 from the Udorn parent after the initial co-infection and this bias towards Udorn PB1 was maintained after two further passages. Included in these were certain gene constellations containing Udorn HA, NA, and PB1 that confered low replicative fitness yet rapidly became dominant at the expense of more fit progeny, even when co-infection ratios of the two viruses favoured PR8. Fitness was not compromised, however, in the corresponding reassortants that also contained Udorn NP. Of particular note is the observation that relatively unfit reassortants could still fulfil the role of vaccine seed candidates as they provided high haemagglutinin (HA) antigen yields through co-production of non-infectious particles and/or by more HA molecules per virion. Our data illustrate the dynamics and complexity of reassortment and highlight how major gene segment interactions formed during packaging, in addition to antibody pressure, initially restrict the reassortant viruses that are formed.

Highlights

  • Reassortment, or the swapping of gene segments, is a major mechanism of influenza virus evolution

  • To examine the spectrum of reassortants generated through the initial stages of the classical reassortment process (Figure 1A), the model seasonal strain Udorn (H3N2) was reassorted with the highly egg-adapted Puerto Rico/8/34 (PR8) strain (H1N1) in four different co-infection conditions representing independent experiments (Figure 1B)

  • In this study we utilised a model of vaccine seed production with the aim of assessing the influence of selective pressures on viral reassortment over multiple passages

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Summary

Introduction

Reassortment, or the swapping of gene segments, is a major mechanism of influenza virus evolution. The observed interactions were numerous, with hundreds being detected in the population of virus particles as a whole These findings led us to propose that the ability of the influenza virus genome to utilise different sets of interactions to package one of each of the eight gene segments provides sufficient flexibility to allow reassortment to occur between different influenza viruses. Of this suite of interactions, some were found at very high frequency, indicating these were likely present in the majority of virus particles. This supported the notion that the stronger interactions are preferentially maintained and shape the gene constellations of resulting reassortant progeny

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