High-throughput single-virion DNA-PAINT reveals structural diversity, cooperativity, and flexibility during selective packaging in influenza

TL;DR

This study uses a new imaging technique to reveal how influenza virus segments are packaged, showing cooperative interactions and structural diversity in virus particles.

Contribution

A multiplexed DNA-PAINT method was developed to analyze genome packaging in thousands of individual influenza virus particles.

Findings

Influenza genome assembly involves multiple pathways guided by interacting segment pairs.

Segment pair interactions influence spatial configurations preserved in mature virions.

The method enables quantification of whole segment interactions, not just sequence motifs.

Abstract

Influenza A, a negative-sense RNA virus, has a genome that consists of eight single-stranded RNA segments. Influenza co-infections can result in reassortant viruses that contain gene segments from multiple strains, causing pandemic outbreaks with severe consequences for human health. The outcome of reassortment is likely influenced by a selective sequence-specific genome packaging mechanism. To uncover the contributions of individual segment pairings to selective packaging, we set out to statistically analyse packaging defects and inter-segment distances in individual A/Puerto Rico/8/34 (H1N1) (PR8) virus particles. To enable such analysis, we developed a multiplexed DNA-PAINT approach capable of assessing the segment stoichiometry of >10 000 individual virus particles in one experiment; our approach can also spatially resolve the individual segments inside complete virus particles with a localization precision of ∼10 nm. Our results show the influenza genome can be assembled through multiple pathways in a redundant and cooperative process guided by preferentially interacting segment pairs and aided by synergistic effects that enhance genome assembly, driving it to completion. Our structural evidence indicates that the interaction strength of segment pairs affects the spatial configuration of the gene segments, which appears to be preserved in mature virions. As our method quantified the interactions of whole influenza segments instead of identifying individual sequence-based interactions, our results can serve as a template to quantify the contributions of individual sequence motifs to selective packaging.

Graphical Abstract

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