Abstract

Influenza virus exhibits two morphologies – spherical and filamentous. Strains that have been grown extensively in laboratory substrates are comprised predominantly of spherical virions while clinical or low passage isolates produce a mixture of spheres and filamentous virions of varying lengths. The filamentous morphology can be lost upon continued passage in embryonated chicken eggs, a common laboratory substrate for influenza viruses. The fact that the filamentous morphology is maintained in nature but lost in favor of a spherical morphology in ovo suggests that filaments confer a selective advantage within the infected host that is not necessary for growth in laboratory substrates. Indeed, we have recently shown that filament-producing variant viruses are selected upon passage of the spherical laboratory strain A/Puerto Rico/8/1934 (H1N1) [PR8] in guinea pigs. Toward determining the nature of the selective advantage conferred by filaments, we sought to identify functional differences between spherical and filamentous particles. We compared the wild-type PR8 virus to two previously characterized recombinant PR8 viruses in which single point mutations within M1 confer a filamentous morphology. Our results indicate that these filamentous PR8 mutants have higher neuraminidase activities than the spherical PR8 virus. Conversely, no differences were observed in HAU:PFU or HAU:RNA ratios, binding avidity, sensitivity to immune serum in hemagglutination inhibition assays, or virion stability at elevated temperatures. Based on these results, we propose that the pleomorphic nature of influenza virus particles is important for the optimization of neuraminidase functions in vivo.

Highlights

  • Influenza A virus (IAV) is an enveloped virus containing eight negative-sense RNA gene segments [1]

  • Our findings suggest a role of the viral NA protein in the fitness advantage conferred by filamentous virion morphology: by two independent measures, the two filamentous rPR8 mutants displayed higher neuraminidase activities compared to rPR8wt, but did not differ significantly in binding avidity, inhibition of binding by antiserum, infectivity or thermostability

  • Each of the functional assays that we applied to our spherical and filamentous PR8 viruses required normalization of the input of each virus. This normalization would be achieved by counting virus particles in transmission electron micrographs, but this approach was not practical given that the preparations used were relatively dilute and concentration by centrifugation can alter virus morphology

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Summary

Introduction

Influenza A virus (IAV) is an enveloped virus containing eight negative-sense RNA gene segments [1]. It is the causative agent of seasonal epidemics of respiratory illness as well as occasional pandemics, the most recent of which occurred in 2009 [2]. IAV is pleomorphic, producing virions of spherical and filamentous morphology [3]. Strains that produce predominantly spherical or ovoid virions have typically been passaged many times within laboratory substrates, while filament-producing strains occur in primary or low passage isolates [4,5]. We define filaments as any virion 300 nm in length or longer ($3x the diameter of a typical spherical virion). Studies performed using reverse genetics systems have identified the M1 matrix protein as the major genetic determinant of virion morphology, portions of the viral nucleoprotein (NP) as well as the cytoplasmic tails of the M2 ion channel, hemagglutinin (HA) and neuraminidase (NA) proteins have been shown to affect virion morphology as well [7,8,9,10,11,12,13]

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