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Evidence That the Heterogeneity of a T4 Population Is the Result of Heritable Traits
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 slo...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4281060/ https://www.ncbi.nlm.nih.gov/pubmed/25551763 http://dx.doi.org/10.1371/journal.pone.0116235 |
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author | Storms, Zachary J. Sauvageau, Dominic |
author_facet | Storms, Zachary J. Sauvageau, Dominic |
author_sort | Storms, Zachary J. |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-4281060 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-42810602015-01-07 Evidence That the Heterogeneity of a T4 Population Is the Result of Heritable Traits Storms, Zachary J. Sauvageau, Dominic PLoS One Research Article 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. Public Library of Science 2014-12-31 /pmc/articles/PMC4281060/ /pubmed/25551763 http://dx.doi.org/10.1371/journal.pone.0116235 Text en © 2014 Storms, Sauvageau http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Storms, Zachary J. Sauvageau, Dominic Evidence That the Heterogeneity of a T4 Population Is the Result of Heritable Traits |
title | Evidence That the Heterogeneity of a T4 Population Is the Result of Heritable Traits |
title_full | Evidence That the Heterogeneity of a T4 Population Is the Result of Heritable Traits |
title_fullStr | Evidence That the Heterogeneity of a T4 Population Is the Result of Heritable Traits |
title_full_unstemmed | Evidence That the Heterogeneity of a T4 Population Is the Result of Heritable Traits |
title_short | Evidence That the Heterogeneity of a T4 Population Is the Result of Heritable Traits |
title_sort | evidence that the heterogeneity of a t4 population is the result of heritable traits |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4281060/ https://www.ncbi.nlm.nih.gov/pubmed/25551763 http://dx.doi.org/10.1371/journal.pone.0116235 |
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