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Rates of Mutation and Recombination in Siphoviridae Phage Genome Evolution over Three Decades

The evolution of asexual organisms is driven not only by the inheritance of genetic modification but also by the acquisition of foreign DNA. The contribution of vertical and horizontal processes to genome evolution depends on their rates per year and is quantified by the ratio of recombination to mu...

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Autores principales: Kupczok, Anne, Neve, Horst, Huang, Kun D, Hoeppner, Marc P, Heller, Knut J, Franz, Charles M A P, Dagan, Tal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5913663/
https://www.ncbi.nlm.nih.gov/pubmed/29688542
http://dx.doi.org/10.1093/molbev/msy027
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author Kupczok, Anne
Neve, Horst
Huang, Kun D
Hoeppner, Marc P
Heller, Knut J
Franz, Charles M A P
Dagan, Tal
author_facet Kupczok, Anne
Neve, Horst
Huang, Kun D
Hoeppner, Marc P
Heller, Knut J
Franz, Charles M A P
Dagan, Tal
author_sort Kupczok, Anne
collection PubMed
description The evolution of asexual organisms is driven not only by the inheritance of genetic modification but also by the acquisition of foreign DNA. The contribution of vertical and horizontal processes to genome evolution depends on their rates per year and is quantified by the ratio of recombination to mutation. These rates have been estimated for bacteria; however, no estimates have been reported for phages. Here, we delineate the contribution of mutation and recombination to dsDNA phage genome evolution. We analyzed 34 isolates of the 936 group of Siphoviridae phages using a Lactococcus lactis strain from a single dairy over 29 years. We estimate a constant substitution rate of 1.9 × 10(−4) substitutions per site per year due to mutation that is within the range of estimates for eukaryotic RNA and DNA viruses. The reconstruction of recombination events reveals a constant rate of five recombination events per year and 4.5 × 10(−3) nucleotide alterations due to recombination per site per year. Thus, the recombination rate exceeds the substitution rate, resulting in a relative effect of recombination to mutation (r/m) of ∼24 that is homogenous over time. Especially in the early transcriptional region, we detect frequent gene loss and regain due to recombination with phages of the 936 group, demonstrating the role of the 936 group pangenome as a reservoir of genetic variation. The observed substitution rate homogeneity conforms to the neutral theory of evolution; hence, the neutral theory can be applied to phage genome evolution and also to genetic variation brought about by recombination.
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spelling pubmed-59136632018-04-30 Rates of Mutation and Recombination in Siphoviridae Phage Genome Evolution over Three Decades Kupczok, Anne Neve, Horst Huang, Kun D Hoeppner, Marc P Heller, Knut J Franz, Charles M A P Dagan, Tal Mol Biol Evol Discoveries The evolution of asexual organisms is driven not only by the inheritance of genetic modification but also by the acquisition of foreign DNA. The contribution of vertical and horizontal processes to genome evolution depends on their rates per year and is quantified by the ratio of recombination to mutation. These rates have been estimated for bacteria; however, no estimates have been reported for phages. Here, we delineate the contribution of mutation and recombination to dsDNA phage genome evolution. We analyzed 34 isolates of the 936 group of Siphoviridae phages using a Lactococcus lactis strain from a single dairy over 29 years. We estimate a constant substitution rate of 1.9 × 10(−4) substitutions per site per year due to mutation that is within the range of estimates for eukaryotic RNA and DNA viruses. The reconstruction of recombination events reveals a constant rate of five recombination events per year and 4.5 × 10(−3) nucleotide alterations due to recombination per site per year. Thus, the recombination rate exceeds the substitution rate, resulting in a relative effect of recombination to mutation (r/m) of ∼24 that is homogenous over time. Especially in the early transcriptional region, we detect frequent gene loss and regain due to recombination with phages of the 936 group, demonstrating the role of the 936 group pangenome as a reservoir of genetic variation. The observed substitution rate homogeneity conforms to the neutral theory of evolution; hence, the neutral theory can be applied to phage genome evolution and also to genetic variation brought about by recombination. Oxford University Press 2018-05 2018-02-22 /pmc/articles/PMC5913663/ /pubmed/29688542 http://dx.doi.org/10.1093/molbev/msy027 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Discoveries
Kupczok, Anne
Neve, Horst
Huang, Kun D
Hoeppner, Marc P
Heller, Knut J
Franz, Charles M A P
Dagan, Tal
Rates of Mutation and Recombination in Siphoviridae Phage Genome Evolution over Three Decades
title Rates of Mutation and Recombination in Siphoviridae Phage Genome Evolution over Three Decades
title_full Rates of Mutation and Recombination in Siphoviridae Phage Genome Evolution over Three Decades
title_fullStr Rates of Mutation and Recombination in Siphoviridae Phage Genome Evolution over Three Decades
title_full_unstemmed Rates of Mutation and Recombination in Siphoviridae Phage Genome Evolution over Three Decades
title_short Rates of Mutation and Recombination in Siphoviridae Phage Genome Evolution over Three Decades
title_sort rates of mutation and recombination in siphoviridae phage genome evolution over three decades
topic Discoveries
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5913663/
https://www.ncbi.nlm.nih.gov/pubmed/29688542
http://dx.doi.org/10.1093/molbev/msy027
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