Long read sequencing reveals poxvirus evolution through rapid homogenization of gene arrays

Large DNA viruses rapidly evolve to defeat host defenses. Poxvirus adaptation can involve combinations of recombination-driven gene copy number variation and beneficial single nucleotide variants (SNVs) at the same locus, yet how these distinct mechanisms of genetic diversification might simultaneously facilitate adaptation to immune blocks is unknown. We performed experimental evolution with a vaccinia virus population harboring a SNV in a gene actively undergoing copy number amplification. Comparisons of virus genomes using the Oxford Nanopore Technologies sequencing platform allowed us to phase SNVs within large gene copy arrays for the first time, and uncovered a mechanism of adaptive SNV homogenization reminiscent of gene conversion, which is actively driven by selection. Our work reveals a new mechanism for the fluid gain of beneficial mutations in genetic regions undergoing active recombination in viruses, and illustrates the value of long read sequencing technologies for investigating complex genome dynamics in diverse biological systems.

[1]  C. Suttle,et al.  The kinetoplastid-infecting Bodo saltans virus (BsV), a window into the most abundant giant viruses in the sea , 2017, bioRxiv.

[2]  Robert E. White,et al.  Heterogeneity of the Epstein-Barr Virus (EBV) Major Internal Repeat Reveals Evolutionary Mechanisms of EBV and a Functional Defect in the Prototype EBV Strain B95-8 , 2017, Journal of Virology.

[3]  Guan-Zhu Han,et al.  Extent and evolution of gene duplication in DNA viruses. , 2017, Virus research.

[4]  Brent S. Pedersen,et al.  Nanopore sequencing and assembly of a human genome with ultra-long reads , 2017, Nature Biotechnology.

[5]  Zev N. Kronenberg,et al.  Emergence of a Viral RNA Polymerase Variant during Gene Copy Number Amplification Promotes Rapid Evolution of Vaccinia Virus , 2016, Journal of Virology.

[6]  J. Filée Genomic comparison of closely related Giant Viruses supports an accordion-like model of evolution , 2015, Front. Microbiol..

[7]  N. Loman,et al.  A complete bacterial genome assembled de novo using only nanopore sequencing data , 2015, Nature Methods.

[8]  C. Ellison,et al.  Non-allelic gene conversion enables rapid evolutionary change at multiple regulatory sites encoded by transposable elements , 2015, eLife.

[9]  B. Moss,et al.  Duplication of the A17L Locus of Vaccinia Virus Provides an Alternate Route to Rifampin Resistance , 2014, Journal of Virology.

[10]  Aaron R. Quinlan,et al.  Poretools: a toolkit for analyzing nanopore sequence data , 2014, bioRxiv.

[11]  U. Ramakrishnan,et al.  Asymmetric patterns of reassortment and concerted evolution in Cardamom bushy dwarf virus. , 2014, Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases.

[12]  Ira M. Hall,et al.  SAMBLASTER: fast duplicate marking and structural variant read extraction , 2014, Bioinform..

[13]  Jay Shendure,et al.  Adaptive Gene Amplification As an Intermediate Step in the Expansion of Virus Host Range , 2014, PLoS pathogens.

[14]  David H. Evans,et al.  Genome Scale Patterns of Recombination between Coinfecting Vaccinia Viruses , 2014, Journal of Virology.

[15]  Heng Li Aligning sequence reads, clone sequences and assembly contigs with BWA-MEM , 2013, 1303.3997.

[16]  E. Holmes,et al.  Gene duplication is infrequent in the recent evolutionary history of RNA viruses. , 2013, Molecular biology and evolution.

[17]  Jay Shendure,et al.  Poxviruses Deploy Genomic Accordions to Adapt Rapidly against Host Antiviral Defenses , 2012, Cell.

[18]  Gabor T. Marth,et al.  Haplotype-based variant detection from short-read sequencing , 2012, 1207.3907.

[19]  J. Soppa Ploidy and gene conversion in Archaea. , 2011, Biochemical Society transactions.

[20]  Rebecca Toroney Investigating Roles of Unconventional RNA Primary, Secondary, and Tertiary Motifs in Regulation of the Protein Kinase PKR , 2010 .

[21]  T. Ohta Gene Conversion and Evolution of Gene Families: An Overview , 2010, Genes.

[22]  R. Sanjuán,et al.  Viral Mutation Rates , 2010, Journal of Virology.

[23]  B. Moss,et al.  Simultaneous high-resolution analysis of vaccinia virus and host cell transcriptomes by deep RNA sequencing , 2010, Proceedings of the National Academy of Sciences.

[24]  J. Filée Lateral gene transfer, lineage-specific gene expansion and the evolution of Nucleo Cytoplasmic Large DNA viruses. , 2009, Journal of invertebrate pathology.

[25]  S. Elena,et al.  Extremely High Mutation Rate of a Hammerhead Viroid , 2009, Science.

[26]  D. Gammon,et al.  The 3′-to-5′ Exonuclease Activity of Vaccinia Virus DNA Polymerase Is Essential and Plays a Role in Promoting Virus Genetic Recombination , 2009, Journal of Virology.

[27]  David C. Krakauer,et al.  Complete Genome Viral Phylogenies Suggests the Concerted Evolution of Regulatory Cores and Accessory Satellites , 2008, PloS one.

[28]  S. Mano,et al.  The Evolutionary Rate of Duplicated Genes Under Concerted Evolution , 2008, Genetics.

[29]  D. Cooper,et al.  Gene conversion: mechanisms, evolution and human disease , 2007, Nature Reviews Genetics.

[30]  T. Eickbush,et al.  Finely Orchestrated Movements: Evolution of the Ribosomal RNA Genes , 2007, Genetics.

[31]  H. Yeh,et al.  Reassortment and Concerted Evolution in Banana Bunchy Top Virus Genomes , 2006, Journal of Virology.

[32]  Naruya Saitou,et al.  Genome-Wide Search of Gene Conversions in Duplicated Genes of Mouse and Rat , 2006 .

[33]  David H. Evans,et al.  Enzymatic processing of replication and recombination intermediates by the vaccinia virus DNA polymerase , 2005, Nucleic acids research.

[34]  E. Holmes,et al.  The evolution of large DNA viruses: combining genomic information of viruses and their hosts. , 2004, Trends in microbiology.

[35]  A. Hughes Birth-and-death evolution of protein-coding regions and concerted evolution of non-coding regions in the multi-component genomes of nanoviruses. , 2004, Molecular phylogenetics and evolution.

[36]  D. Rock,et al.  The Genome of Canarypox Virus , 2004, Journal of Virology.

[37]  Brandon S. Gaut,et al.  Extensive gene gain associated with adaptive evolution of poxviruses , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[38]  Steve Rozen,et al.  Abundant gene conversion between arms of palindromes in human and ape Y chromosomes , 2003, Nature.

[39]  Guy Drouin,et al.  Characterization of the Gene Conversions Between the Multigene Family Members of the Yeast Genome , 2002, Journal of Molecular Evolution.

[40]  J. Haber,et al.  Lucky breaks: analysis of recombination in Saccharomyces. , 2000, Mutation research.

[41]  D. Rock,et al.  The Genome of Fowlpox Virus , 2000, Journal of Virology.

[42]  Lukas Wagner,et al.  A Greedy Algorithm for Aligning DNA Sequences , 2000, J. Comput. Biol..

[43]  D H Evans,et al.  Vaccinia virus DNA polymerase promotes DNA pairing and strand-transfer reactions. , 1999, Virology.

[44]  Kenneth H. Wolfe,et al.  Gene Duplication and Gene Conversion in the Caenorhabditis elegans Genome , 1999, Journal of Molecular Evolution.

[45]  J. Silverman,et al.  Regulation of the protein kinase PKR by the vaccinia virus pseudosubstrate inhibitor K3L is dependent on residues conserved between the K3L protein and the PKR substrate eIF2alpha , 1997, Molecular and cellular biology.

[46]  Norman Arnheim,et al.  New HLA–DPB1 alleles generated by interallelic gene conversion detected by analysis of sperm , 1995, Nature Genetics.

[47]  M. Perkus,et al.  Reversal of the interferon-sensitive phenotype of a vaccinia virus lacking E3L by expression of the reovirus S4 gene , 1995, Journal of virology.

[48]  H. W. Chang,et al.  The E3L gene of vaccinia virus encodes an inhibitor of the interferon-induced, double-stranded RNA-dependent protein kinase. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[49]  O. Elroy-Stein,et al.  The vaccinia virus K3L gene product potentiates translation by inhibiting double-stranded-RNA-activated protein kinase and phosphorylation of the alpha subunit of eukaryotic initiation factor 2 , 1992, Journal of virology.

[50]  E. Paoletti,et al.  Extrachromosomal recombination in vaccinia-infected cells requires a functional DNA polymerase participating at a level other than DNA replication. , 1990, Virus research.

[51]  S. Goebel,et al.  The complete DNA sequence of vaccinia virus. , 1990, Virology.

[52]  C. Mathews,et al.  Amplification of the ribonucleotide reductase small subunit gene: analysis of novel joints and the mechanism of gene duplication in vaccinia virus. , 1989, Nucleic acids research.

[53]  M. Merchlinsky,et al.  Intramolecular homologous recombination in cells infected with temperature-sensitive mutants of vaccinia virus , 1989, Journal of virology.

[54]  D. Panicali,et al.  Delineation of the viral products of recombination in vaccinia virus-infected cells , 1988, Journal of virology.

[55]  G. McFadden,et al.  High levels of genetic recombination among cotransfected plasmid DNAs in poxvirus-infected mammalian cells , 1988, Journal of virology.

[56]  L. A. Ball,et al.  High-frequency homologous recombination in vaccinia virus DNA , 1987, Journal of virology.

[57]  J. Crow,et al.  Just and Unjust: E. E. Just (1883–1941) , 1987, Genetics.

[58]  R. Condit,et al.  The preparation of orthopoxvirus DNA. , 1981, Journal of virological methods.

[59]  P. C. Wensink,et al.  A comparison of the ribosomal DNA's of Xenopus laevis and Xenopus mulleri: the evolution of tandem genes. , 1972, Journal of molecular biology.

[60]  Dr. Susumu Ohno Evolution by Gene Duplication , 1970, Springer Berlin Heidelberg.

[61]  H. Drexler,et al.  Identification and verification of rodent cell lines by polymerase chain reaction , 2007, Cytotechnology.

[62]  David Romero,et al.  Gene conversion and concerted evolution in bacterial genomes. , 2005, FEMS microbiology reviews.

[63]  D. Liao,et al.  Concerted evolution: molecular mechanism and biological implications. , 1999, American journal of human genetics.

[64]  T. Petes,et al.  Recombination between repeated genes in microorganisms. , 1988, Annual review of genetics.