High frequency of mutations that expand the host range of an RNA virus

被引:68
作者
Ferris, Martin T.
Joyce, Paul
Burch, Christina L.
机构
[1] Univ N Carolina, Dept Biol, Chapel Hill, NC 27599 USA
[2] Univ Idaho, Dept Math, Moscow, ID 83844 USA
[3] Univ Idaho, Dept Stat, Moscow, ID 83844 USA
关键词
D O I
10.1534/genetics.106.064634
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The ability of a virus population to colonize a novel host is predicted to depend on the equilibrium frequency of potential colonists (i.e., genotypes capable of infecting the novel host) in the source population. In this Study,,e investigated the determinants of the equilibrium frequency of potential colonists in the RNA bacteriophage phi 6. We isolated 40 spontaneous mutants capable of infecting a novel Pseudomonas syringae host and sequenced their host attachment genes to identify the responsible mutations. We observed 16 different mutations in the host attachment gene and used a new statistical approach to estimate that 39 additional mutations were missed by our screen. Phenotypic and fitness assays confirmed that the proximate mechanism underlying host range expansion was an increase in the ability to attach to the novel host and that acquisition of this ability most often imposed a cost for growth rate on two standard hosts. Considered in a population genetic framework, our data suggest that host range mutations should exist in phage populations at an equilibrium frequency (3 x 10(-4)) that exceeds the phage mutation rate by more than two orders of magnitude. Thus, colonization of novel hosts is unlikely to be limited by an inability to produce appropriate mutations.
引用
收藏
页码:1013 / 1022
页数:10
相关论文
共 45 条
  • [1] The role of evolution in the emergence of infectious diseases
    Antia, R
    Regoes, RR
    Koella, JC
    Bergstrom, CT
    [J]. NATURE, 2003, 426 (6967) : 658 - 661
  • [2] SINGLE AMINO-ACID SUBSTITUTIONS IN THE HEMAGGLUTININ CAN ALTER THE HOST RANGE AND RECEPTOR-BINDING PROPERTIES OF H1-STRAINS OF INFLUENZA-A VIRUS
    AYTAY, S
    SCHULZE, IT
    [J]. JOURNAL OF VIROLOGY, 1991, 65 (06) : 3022 - 3028
  • [3] Evolution of cell recognition by viruses
    Baranowski, E
    Ruiz-Jarabo, CM
    Domingo, E
    [J]. SCIENCE, 2001, 292 (5519) : 1102 - 1105
  • [4] Experimental estimate of the abundance and effects of nearly neutral mutations in the RNA virus φ6
    Burch, Christina L.
    Guyader, Sebastien
    Samarov, Daniel
    Shen, Haipeng
    [J]. GENETICS, 2007, 176 (01) : 467 - 476
  • [5] Epistasis and its relationship to canalization in the RNA virus φ6
    Burch, CL
    Chao, L
    [J]. GENETICS, 2004, 167 (02) : 559 - 567
  • [6] Chao L, 1997, GENETICS, V147, P953
  • [7] Distribution of spontaneous mutants and inferences about the replication mode of the RNA bacteriophage φ6
    Chao, L
    Rang, CU
    Wong, LE
    [J]. JOURNAL OF VIROLOGY, 2002, 76 (07) : 3276 - 3281
  • [8] FITNESS OF RNA VIRUS DECREASED BY MULLER RATCHET
    CHAO, L
    [J]. NATURE, 1990, 348 (6300) : 454 - 455
  • [9] Mouse adaptation determinants of poliovirus type 1 enhance viral uncoating
    Couderc, T
    Delpeyroux, F
    LeBlay, H
    Blondel, B
    [J]. JOURNAL OF VIROLOGY, 1996, 70 (01) : 305 - 312
  • [10] The variant call format and VCFtools
    Danecek, Petr
    Auton, Adam
    Abecasis, Goncalo
    Albers, Cornelis A.
    Banks, Eric
    DePristo, Mark A.
    Handsaker, Robert E.
    Lunter, Gerton
    Marth, Gabor T.
    Sherry, Stephen T.
    McVean, Gilean
    Durbin, Richard
    [J]. BIOINFORMATICS, 2011, 27 (15) : 2156 - 2158