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Experimental evolution of UV resistance in a phage

The dsDNA bacteriophage T7 was subjected to 30 cycles of lethal ultraviolet light (UV) exposure to select increased resistance to UV. The exposure effected a 0.9999 kill of the ancestral population, and survival of the ending population was nearly 50-fold improved. At the end point, a 2.1 kb deletio...

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Detalles Bibliográficos
Autores principales: Tom, Eric F., Molineux, Ian J., Paff, Matthew L., Bull, James J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6042481/
https://www.ncbi.nlm.nih.gov/pubmed/30013847
http://dx.doi.org/10.7717/peerj.5190
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author Tom, Eric F.
Molineux, Ian J.
Paff, Matthew L.
Bull, James J.
author_facet Tom, Eric F.
Molineux, Ian J.
Paff, Matthew L.
Bull, James J.
author_sort Tom, Eric F.
collection PubMed
description The dsDNA bacteriophage T7 was subjected to 30 cycles of lethal ultraviolet light (UV) exposure to select increased resistance to UV. The exposure effected a 0.9999 kill of the ancestral population, and survival of the ending population was nearly 50-fold improved. At the end point, a 2.1 kb deletion of early genes and three substitutions in structural-genes were the only changes observed at high frequency throughout the 40 kb genome; no changes were observed in genes affecting DNA metabolism. The deletion accounted for only a two-fold improvement in survival. One possible explanation of its benefit is that it represents an error catastrophe, whereby the genome experiences a reduced mutation rate. The mechanism of benefit provided by the three structural-gene mutations remains unknown. The results offer some hope of artificially evolving greater protection against sunlight damage in applications of phage therapy to plants, but the response of T7 is weak compared to that observed in bacteria selected to resist ionizing radiation. Because of the weak response, mathematical analysis of the selection process was performed to determine how the protocol might have been modified to achieve a greater response, but the greatest protection may well come from evolving phages to bind materials that block the UV.
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spelling pubmed-60424812018-07-16 Experimental evolution of UV resistance in a phage Tom, Eric F. Molineux, Ian J. Paff, Matthew L. Bull, James J. PeerJ Genetics The dsDNA bacteriophage T7 was subjected to 30 cycles of lethal ultraviolet light (UV) exposure to select increased resistance to UV. The exposure effected a 0.9999 kill of the ancestral population, and survival of the ending population was nearly 50-fold improved. At the end point, a 2.1 kb deletion of early genes and three substitutions in structural-genes were the only changes observed at high frequency throughout the 40 kb genome; no changes were observed in genes affecting DNA metabolism. The deletion accounted for only a two-fold improvement in survival. One possible explanation of its benefit is that it represents an error catastrophe, whereby the genome experiences a reduced mutation rate. The mechanism of benefit provided by the three structural-gene mutations remains unknown. The results offer some hope of artificially evolving greater protection against sunlight damage in applications of phage therapy to plants, but the response of T7 is weak compared to that observed in bacteria selected to resist ionizing radiation. Because of the weak response, mathematical analysis of the selection process was performed to determine how the protocol might have been modified to achieve a greater response, but the greatest protection may well come from evolving phages to bind materials that block the UV. PeerJ Inc. 2018-07-09 /pmc/articles/PMC6042481/ /pubmed/30013847 http://dx.doi.org/10.7717/peerj.5190 Text en © 2018 Tom et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Genetics
Tom, Eric F.
Molineux, Ian J.
Paff, Matthew L.
Bull, James J.
Experimental evolution of UV resistance in a phage
title Experimental evolution of UV resistance in a phage
title_full Experimental evolution of UV resistance in a phage
title_fullStr Experimental evolution of UV resistance in a phage
title_full_unstemmed Experimental evolution of UV resistance in a phage
title_short Experimental evolution of UV resistance in a phage
title_sort experimental evolution of uv resistance in a phage
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6042481/
https://www.ncbi.nlm.nih.gov/pubmed/30013847
http://dx.doi.org/10.7717/peerj.5190
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