Literature DB >> 35044211

Contribution of RNA-RNA Interactions Mediated by the Genome Packaging Signals for the Selective Genome Packaging of Influenza A Virus.

Sho Miyamoto1,2, Yukiko Muramoto1,3,4, Keiko Shindo1, Yoko Fujita-Fujiharu1,3,4, Takeshi Morikawa1, Ryoma Tamura1,3, Jamie L Gilmore1, Masahiro Nakano1,3,4, Takeshi Noda1,3,4.   

Abstract

The influenza A virus genome is composed of eight single-stranded negative-sense viral RNA segments (vRNAs). The eight vRNAs are selectively packaged into each progeny virion. This process likely involves specific interactions between the vRNAs via segment-specific packaging signals located in both the 3'- and 5'-terminal regions of the respective vRNAs. To assess the importance of vRNA-vRNA interactions via packaging signals for selective genome packaging, we generated mutant viruses possessing silent mutations in the packaging signal region of the hemagglutinin (HA) vRNA. A mutant virus possessing silent mutations in nucleotides (nt) 1664 to 1676 resulted in defects in HA vRNA incorporation and showed a reduction in viral growth. After serial passage, the mutant virus acquired additional mutations in the 5'-terminal packaging signal regions of both the HA and polymerase basic 2 (PB2) vRNAs. These mutations contributed to the recovery of viral growth and HA vRNA packaging efficiency. In addition, an RNA-RNA interaction between the 5' ends of HA and PB2 vRNAs was confirmed in vitro, and this interaction was disrupted following the introduction of silent mutations in the HA vRNA. Thus, our results demonstrated that RNA-RNA interactions between the packaging signal regions of HA vRNA and PB2 vRNA are important for selective genome packaging. IMPORTANCE While numerous viral genomes comprise a single genome segment, the influenza A virus possesses eight segmented genomes. Influenza A virus can benefit from having a segmented genome because the segments can reassort with other strains of the influenza virus to create new genetically distinct strains. The influenza A virus efficiently incorporates one copy of each of its eight genomic segments per viral particle. However, the mechanism by which each segment is specifically selected is poorly understood. The genome segments contain RNA signals that facilitate the incorporation of segments into virus particles. These regions may facilitate specific interactions between the genome segments, creating an eight-segment complex, which can then be packaged into individual particles. In this study, we provide evidence that RNA signals contribute to specific interactions between two of the influenza virus genome segments.

Entities:  

Keywords:  genome; genome packaging; influenza virus

Mesh:

Substances:

Year:  2022        PMID: 35044211      PMCID: PMC8941900          DOI: 10.1128/JVI.01641-21

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   6.549


  40 in total

1.  The influenza A virus PB2, PA, NP, and M segments play a pivotal role during genome packaging.

Authors:  Qinshan Gao; Yi-Ying Chou; Sultan Doğanay; Reza Vafabakhsh; Taekjip Ha; Peter Palese
Journal:  J Virol       Date:  2012-04-24       Impact factor: 5.103

2.  Nucleotide sequence requirements at the 5' end of the influenza A virus M RNA segment for efficient virus replication.

Authors:  Makoto Ozawa; Junko Maeda; Kiyoko Iwatsuki-Horimoto; Shinji Watanabe; Hideo Goto; Taisuke Horimoto; Yoshihiro Kawaoka
Journal:  J Virol       Date:  2009-01-21       Impact factor: 5.103

3.  Genetic applications of an inverse polymerase chain reaction.

Authors:  H Ochman; A S Gerber; D L Hartl
Journal:  Genetics       Date:  1988-11       Impact factor: 4.562

4.  Identification of potential conserved RNA secondary structure throughout influenza A coding regions.

Authors:  Walter N Moss; Salvatore F Priore; Douglas H Turner
Journal:  RNA       Date:  2011-05-02       Impact factor: 4.942

5.  The structure of the influenza A virus genome.

Authors:  Bernadeta Dadonaite; Brad Gilbertson; Michael L Knight; Sanja Trifkovic; Steven Rockman; Alain Laederach; Lorena E Brown; Ervin Fodor; David L V Bauer
Journal:  Nat Microbiol       Date:  2019-07-22       Impact factor: 17.745

6.  Exploitation of nucleic acid packaging signals to generate a novel influenza virus-based vector stably expressing two foreign genes.

Authors:  Tokiko Watanabe; Shinji Watanabe; Takeshi Noda; Yutaka Fujii; Yoshihiro Kawaoka
Journal:  J Virol       Date:  2003-10       Impact factor: 5.103

7.  SWAN: sliding window analysis of nucleotide sequence variability.

Authors:  V Proutski; E Holmes
Journal:  Bioinformatics       Date:  1998-06       Impact factor: 6.937

8.  Codon usage bias and the evolution of influenza A viruses. Codon Usage Biases of Influenza Virus.

Authors:  Emily H M Wong; David K Smith; Raul Rabadan; Malik Peiris; Leo L M Poon
Journal:  BMC Evol Biol       Date:  2010-08-19       Impact factor: 3.260

9.  Characterisation of influenza A viruses with mutations in segment 5 packaging signals.

Authors:  Edward C Hutchinson; Helen M Wise; Katerine Kudryavtseva; Martin D Curran; Paul Digard
Journal:  Vaccine       Date:  2009-10-23       Impact factor: 3.641

10.  Pandemic influenza A virus codon usage revisited: biases, adaptation and implications for vaccine strain development.

Authors:  Natalia Goñi; Andrés Iriarte; Victoria Comas; Martín Soñora; Pilar Moreno; Gonzalo Moratorio; Héctor Musto; Juan Cristina
Journal:  Virol J       Date:  2012-11-08       Impact factor: 4.099

View more
  1 in total

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

Authors:  Celia Jakob; Rithu Paul-Stansilaus; Martin Schwemmle; Roland Marquet; Hardin Bolte
Journal:  Nucleic Acids Res       Date:  2022-08-22       Impact factor: 19.160

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.