Literature DB >> 25713211

Positive Selection Drives Preferred Segment Combinations during Influenza Virus Reassortment.

Konstantin B Zeldovich1, Ping Liu2, Nicholas Renzette3, Matthieu Foll4, Serena T Pham2, Sergey V Venev1, Glen R Gallagher2, Daniel N Bolon5, Evelyn A Kurt-Jones2, Jeffrey D Jensen4, Daniel R Caffrey2, Celia A Schiffer5, Timothy F Kowalik3, Jennifer P Wang6, Robert W Finberg2.   

Abstract

Influenza A virus (IAV) has a segmented genome that allows for the exchange of genome segments between different strains. This reassortment accelerates evolution by breaking linkage, helping IAV cross species barriers to potentially create highly virulent strains. Challenges associated with monitoring the process of reassortment in molecular detail have limited our understanding of its evolutionary implications. We applied a novel deep sequencing approach with quantitative analysis to assess the in vitro temporal evolution of genomic reassortment in IAV. The combination of H1N1 and H3N2 strains reproducibly generated a new H1N2 strain with the hemagglutinin and nucleoprotein segments originating from H1N1 and the remaining six segments from H3N2. By deep sequencing the entire viral genome, we monitored the evolution of reassortment, quantifying the relative abundance of all IAV genome segments from the two parent strains over time and measuring the selection coefficients of the reassorting segments. Additionally, we observed several mutations coemerging with reassortment that were not found during passaging of pure parental IAV strains. Our results demonstrate how reassortment of the segmented genome can accelerate viral evolution in IAV, potentially enabled by the emergence of a small number of individual mutations.
© The Author 2015. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

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Keywords:  deep sequencing; evolution; influenza; mutations; reassortment

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Year:  2015        PMID: 25713211      PMCID: PMC4462674          DOI: 10.1093/molbev/msv044

Source DB:  PubMed          Journal:  Mol Biol Evol        ISSN: 0737-4038            Impact factor:   16.240


  37 in total

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10.  Genetic compatibility and virulence of reassortants derived from contemporary avian H5N1 and human H3N2 influenza A viruses.

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Journal:  PLoS Pathog       Date:  2008-05-23       Impact factor: 6.823

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Authors:  Kristina L Prachanronarong; Aneth S Canale; Ping Liu; Mohan Somasundaran; Shurong Hou; Yu-Ping Poh; Thomas Han; Quan Zhu; Nicholas Renzette; Konstantin B Zeldovich; Timothy F Kowalik; Nese Kurt-Yilmaz; Jeffrey D Jensen; Daniel N A Bolon; Wayne A Marasco; Robert W Finberg; Celia A Schiffer; Jennifer P Wang
Journal:  J Virol       Date:  2019-01-04       Impact factor: 5.103

2.  Influenza A virus preferentially snatches noncoding RNA caps.

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3.  The effective rate of influenza reassortment is limited during human infection.

Authors:  Ashley Sobel Leonard; Micah T McClain; Gavin J D Smith; David E Wentworth; Rebecca A Halpin; Xudong Lin; Amy Ransier; Timothy B Stockwell; Suman R Das; Anthony S Gilbert; Rob Lambkin-Williams; Geoffrey S Ginsburg; Christopher W Woods; Katia Koelle; Christopher J R Illingworth
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5.  Evolutionary conservation and positive selection of influenza A nucleoprotein CTL epitopes for universal vaccination.

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Review 6.  Experimental Approaches to Study Genome Packaging of Influenza A Viruses.

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Review 7.  Mutation and Epistasis in Influenza Virus Evolution.

Authors:  Daniel M Lyons; Adam S Lauring
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8.  Live bird markets as evolutionary epicentres of H9N2 low pathogenicity avian influenza viruses in Korea.

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9.  Intragenic recombination influences rotavirus diversity and evolution.

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