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Genetically Determined Variation in Lysis Time Variance in the Bacteriophage φX174.
Baker, Christopher W; Miller, Craig R; Thaweethai, Tanayott; Yuan, Jeffrey; Baker, Meghan Hollibaugh; Joyce, Paul; Weinreich, Daniel M.
Afiliação
  • Baker CW; Department of Ecology and Evolutionary Biology, Brown University, Providence, Rhode Island 02912 baker03@g.harvard.edu.
  • Miller CR; Department of Mathematics, University of Idaho, Moscow, Idaho 83844 Department of Biological Sciences, University of Idaho, Moscow, Idaho 83844 Center for Modeling Complex Interactions, University of Idaho, Moscow, Idaho 83844.
  • Thaweethai T; Department of Ecology and Evolutionary Biology, Brown University, Providence, Rhode Island 02912.
  • Yuan J; Department of Ecology and Evolutionary Biology, Brown University, Providence, Rhode Island 02912.
  • Baker MH; Department of Ecology and Evolutionary Biology, Brown University, Providence, Rhode Island 02912.
  • Joyce P; Department of Mathematics, University of Idaho, Moscow, Idaho 83844.
  • Weinreich DM; Department of Ecology and Evolutionary Biology, Brown University, Providence, Rhode Island 02912 Center for Computational Molecular Biology, Brown University, Providence, Rhode Island 02912.
G3 (Bethesda) ; 6(4): 939-55, 2016 04 07.
Article em En | MEDLINE | ID: mdl-26921293
ABSTRACT
Researchers in evolutionary genetics recently have recognized an exciting opportunity in decomposing beneficial mutations into their proximal, mechanistic determinants. The application of methods and concepts from molecular biology and life history theory to studies of lytic bacteriophages (phages) has allowed them to understand how natural selection sees mutations influencing life history. This work motivated the research presented here, in which we explored whether, under consistent experimental conditions, small differences in the genome of bacteriophage φX174 could lead to altered life history phenotypes among a panel of eight genetically distinct clones. We assessed the clones' phenotypes by applying a novel statistical framework to the results of a serially sampled parallel infection assay, in which we simultaneously inoculated each of a large number of replicate host volumes with ∼1 phage particle. We sequentially plated the volumes over the course of infection and counted the plaques that formed after incubation. These counts served as a proxy for the number of phage particles in a single volume as a function of time. From repeated assays, we inferred significant, genetically determined heterogeneity in lysis time and burst size, including lysis time variance. These findings are interesting in light of the genetic and phenotypic constraints on the single-protein lysis mechanism of φX174. We speculate briefly on the mechanisms underlying our results, and we discuss the potential importance of lysis time variance in viral evolution.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2016 Tipo de documento: Article