Evidence that the heterogeneity of a T4 population is the result of heritable traits.

PLoS One

Department of Chemical and Materials Engineering, University of Alberta, Edmonton, Alberta, Canada.

Published: May 2016

AI Article Synopsis

  • Many bacteriophage populations show variations in how effectively they can attach to host cells, with a small fraction (residual fraction) having slower adsorption rates compared to the main group.
  • Recent research on phage T4 revealed that this residual fraction is not just due to differences in a single genetic type, but rather involves distinct subgroups with inherited traits affecting their adsorption.
  • Genetic analysis identified two specific mutations in gene 37 that altered the structure of the phage’s tail-fiber, which is critical for binding to host cells; these mutations correlated with lower efficiency in attaching to hosts.

Article Abstract

Many bacteriophage populations display heterogeneity in their adsorption characteristics; a portion of the phage population remains free in solution throughout adsorption experiments (residual fraction). This residual fraction generally constitutes a minority of phages that exhibit significantly slower adsorption kinetics than the main phage stock (main fraction). While this phenomenon is likely the result of evolutionary driving forces, the present study demonstrates that the residual fraction is not always the result of phenotypic variations within a single genotype, as is generally thought. Experiments with phage T4 showed that two subgroups with distinct adsorption traits that were passed on to their progeny could be isolated from the original phage stock. Sequencing of genes involved in adsorption revealed two point mutations in gene 37 of residual fraction isolates, which resulted in modifications to the long tail-fiber, the organelle of attachment and host cell recognition. Adsorption studies consistently showed that T4 phage stocks amplified from residual fraction isolates had significantly lower adsorption efficiencies than those amplified from main fractions. The conducted experiments provide convincing evidence that the observed heterogeneity in T4 adsorption behavior is the result of conserved mutations to the phage genome and is not exclusively the result of phenotypic variations within the population. While it is believed high mutation rates exist to hasten phage adaptation, this study shows that this bet hedging strategy can also, in the short term, inadvertently handicap the phage's adsorption capabilities to a given host under normal infection conditions, resulting in the residual fraction observed in adsorption experiments.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4281060PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0116235PLOS

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