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Frequency and Fitness Consequences of Bacteriophage Φ6 Host Range Mutations

Viruses readily mutate and gain the ability to infect novel hosts, but few data are available regarding the number of possible host range-expanding mutations allowing infection of any given novel host, and the fitness consequences of these mutations on original and novel hosts. To gain insight into...

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Autores principales: Ford, Brian E., Sun, Bruce, Carpino, James, Chapler, Elizabeth S., Ching, Jane, Choi, Yoon, Jhun, Kevin, Kim, Jung D., Lallos, Gregory G., Morgenstern, Rachelle, Singh, Shalini, Theja, Sai, Dennehy, John J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4237377/
https://www.ncbi.nlm.nih.gov/pubmed/25409341
http://dx.doi.org/10.1371/journal.pone.0113078
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author Ford, Brian E.
Sun, Bruce
Carpino, James
Chapler, Elizabeth S.
Ching, Jane
Choi, Yoon
Jhun, Kevin
Kim, Jung D.
Lallos, Gregory G.
Morgenstern, Rachelle
Singh, Shalini
Theja, Sai
Dennehy, John J.
author_facet Ford, Brian E.
Sun, Bruce
Carpino, James
Chapler, Elizabeth S.
Ching, Jane
Choi, Yoon
Jhun, Kevin
Kim, Jung D.
Lallos, Gregory G.
Morgenstern, Rachelle
Singh, Shalini
Theja, Sai
Dennehy, John J.
author_sort Ford, Brian E.
collection PubMed
description Viruses readily mutate and gain the ability to infect novel hosts, but few data are available regarding the number of possible host range-expanding mutations allowing infection of any given novel host, and the fitness consequences of these mutations on original and novel hosts. To gain insight into the process of host range expansion, we isolated and sequenced 69 independent mutants of the dsRNA bacteriophage Φ6 able to infect the novel host, Pseudomonas pseudoalcaligenes. In total, we found at least 17 unique suites of mutations among these 69 mutants. We assayed fitness for 13 of 17 mutant genotypes on P. pseudoalcaligenes and the standard laboratory host, P. phaseolicola. Mutants exhibited significantly lower fitnesses on P. pseudoalcaligenes compared to P. phaseolicola. Furthermore, 12 of the 13 assayed mutants showed reduced fitness on P. phaseolicola compared to wildtype Φ6, confirming the prevalence of antagonistic pleiotropy during host range expansion. Further experiments revealed that the mechanistic basis of these fitness differences was likely variation in host attachment ability. In addition, using computational protein modeling, we show that host-range expanding mutations occurred in hotspots on the surface of the phage's host attachment protein opposite a putative hydrophobic anchoring domain.
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spelling pubmed-42373772014-11-21 Frequency and Fitness Consequences of Bacteriophage Φ6 Host Range Mutations Ford, Brian E. Sun, Bruce Carpino, James Chapler, Elizabeth S. Ching, Jane Choi, Yoon Jhun, Kevin Kim, Jung D. Lallos, Gregory G. Morgenstern, Rachelle Singh, Shalini Theja, Sai Dennehy, John J. PLoS One Research Article Viruses readily mutate and gain the ability to infect novel hosts, but few data are available regarding the number of possible host range-expanding mutations allowing infection of any given novel host, and the fitness consequences of these mutations on original and novel hosts. To gain insight into the process of host range expansion, we isolated and sequenced 69 independent mutants of the dsRNA bacteriophage Φ6 able to infect the novel host, Pseudomonas pseudoalcaligenes. In total, we found at least 17 unique suites of mutations among these 69 mutants. We assayed fitness for 13 of 17 mutant genotypes on P. pseudoalcaligenes and the standard laboratory host, P. phaseolicola. Mutants exhibited significantly lower fitnesses on P. pseudoalcaligenes compared to P. phaseolicola. Furthermore, 12 of the 13 assayed mutants showed reduced fitness on P. phaseolicola compared to wildtype Φ6, confirming the prevalence of antagonistic pleiotropy during host range expansion. Further experiments revealed that the mechanistic basis of these fitness differences was likely variation in host attachment ability. In addition, using computational protein modeling, we show that host-range expanding mutations occurred in hotspots on the surface of the phage's host attachment protein opposite a putative hydrophobic anchoring domain. Public Library of Science 2014-11-19 /pmc/articles/PMC4237377/ /pubmed/25409341 http://dx.doi.org/10.1371/journal.pone.0113078 Text en © 2014 Ford 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Ford, Brian E.
Sun, Bruce
Carpino, James
Chapler, Elizabeth S.
Ching, Jane
Choi, Yoon
Jhun, Kevin
Kim, Jung D.
Lallos, Gregory G.
Morgenstern, Rachelle
Singh, Shalini
Theja, Sai
Dennehy, John J.
Frequency and Fitness Consequences of Bacteriophage Φ6 Host Range Mutations
title Frequency and Fitness Consequences of Bacteriophage Φ6 Host Range Mutations
title_full Frequency and Fitness Consequences of Bacteriophage Φ6 Host Range Mutations
title_fullStr Frequency and Fitness Consequences of Bacteriophage Φ6 Host Range Mutations
title_full_unstemmed Frequency and Fitness Consequences of Bacteriophage Φ6 Host Range Mutations
title_short Frequency and Fitness Consequences of Bacteriophage Φ6 Host Range Mutations
title_sort frequency and fitness consequences of bacteriophage φ6 host range mutations
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4237377/
https://www.ncbi.nlm.nih.gov/pubmed/25409341
http://dx.doi.org/10.1371/journal.pone.0113078
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