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The influenza A virus genome packaging network - complex, flexible and yet unsolved

Journal

NUCLEIC ACIDS RESEARCH
Volume 50, Issue 16, Pages 9023-9038

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/nar/gkac688

Keywords

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Funding

  1. French NationalResearch Agency (ANR) [ANR-19-CE11-0027]
  2. GermanResearch Foundation (DFG)
  3. European Union [955974]
  4. FluCode Project [ANR-19-CE11-0027]
  5. Agence Nationale de la Recherche (ANR) [ANR-19-CE11-0027] Funding Source: Agence Nationale de la Recherche (ANR)
  6. Marie Curie Actions (MSCA) [955974] Funding Source: Marie Curie Actions (MSCA)

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The genome of influenza A virus consists of eight unique viral RNA segments, and reassortment events can create new IAVs. Recent research suggests that a viral genome packaging mechanism promotes reassortment by delivering the genome segments into the virus particle. However, there is a current shortage of functionally validated intersegmental RNA-RNA interactions in understanding this mechanism.
The genome of influenza A virus (IAV) consists of eight unique viral RNA segments. This genome organization allows genetic reassortment between co-infecting IAV strains, whereby new IAVs with altered genome segment compositions emerge. While it is known that reassortment events can create pandemic IAVs, it remains impossible to anticipate reassortment outcomes with pandemic prospects. Recent research indicates that reassortment is promoted by a viral genome packaging mechanism that delivers the eight genome segments as a supramolecular complex into the virus particle. This finding holds promise of predicting pandemic IAVs by understanding the intermolecular interactions governing this genome packaging mechanism. Here, we critically review the prevailing mechanistic model postulating that IAV genome packaging is orchestrated by a network of intersegmental RNA-RNA interactions. Although we find supporting evidence, including segment-specific packaging signals and experimentally proposed RNA-RNA interaction networks, this mechanistic model remains debatable due to a current shortage of functionally validated intersegmental RNA-RNA interactions. We speculate that identifying such functional intersegmental RNA-RNA contacts might be hampered by limitations of the utilized probing techniques and the inherent complexity of the genome packaging mechanism. Nevertheless, we anticipate that improved probing strategies combined with a mutagenesis-based validation could facilitate their discovery.

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