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One Year Genome Evolution of Lausannevirus in Allopatric versus Sympatric Conditions

Amoeba-resisting microorganisms raised a great interest during the last decade. Among them, some large DNA viruses present huge genomes up to 2.5 Mb long, exceeding the size of small bacterial genomes. The rate of genome evolution in terms of mutation, deletion, and gene acquisition in these genomes...

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Autores principales: Mueller, Linda, Bertelli, Claire, Pillonel, Trestan, Salamin, Nicolas, Greub, Gilbert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5513546/
https://www.ncbi.nlm.nih.gov/pubmed/28525571
http://dx.doi.org/10.1093/gbe/evx074
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author Mueller, Linda
Bertelli, Claire
Pillonel, Trestan
Salamin, Nicolas
Greub, Gilbert
author_facet Mueller, Linda
Bertelli, Claire
Pillonel, Trestan
Salamin, Nicolas
Greub, Gilbert
author_sort Mueller, Linda
collection PubMed
description Amoeba-resisting microorganisms raised a great interest during the last decade. Among them, some large DNA viruses present huge genomes up to 2.5 Mb long, exceeding the size of small bacterial genomes. The rate of genome evolution in terms of mutation, deletion, and gene acquisition in these genomes is yet unknown. Given the suspected high plasticity of viral genomes, the microevolution of the 346 kb genome of Lausannevirus, a member of Megavirales, was studied. Hence, Lausannevirus was co-cultured within the amoeba Acanthamoeba castellanii over one year. Despite a low number of mutations, the virus showed a genome reduction of 3.7% after 12 months. Lausannevirus genome evolution in sympatric conditions was investigated by its co-culture with Estrella lausannensis, an obligate intracellular bacterium, in the amoeba A. castellanii during one year. Cultures were split every 3 months. Genome sequencing revealed that in these conditions both, Lausannevirus and E. lausannensis, show stable genome, presenting no major rearrangement. In fact, after one year they acquired from 2 to 7 and from 4 to 10 mutations per culture for Lausannevirus and E. lausannensis, respectively. Interestingly, different mutations in the endonuclease encoding genes of Lausannevirus were observed in different subcultures, highlighting the importance of this gene product in the replication of Lausannevirus. Conversely, mutations in E. lausannensis were mainly located in a gene encoding for a phosphoenolpyruvate–protein phosphotransferase (PtsI), implicated in sugar metabolism. Moreover, in our conditions and with our analyses we detected no horizontal gene transfer during one year of co-culture.
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spelling pubmed-55135462017-07-20 One Year Genome Evolution of Lausannevirus in Allopatric versus Sympatric Conditions Mueller, Linda Bertelli, Claire Pillonel, Trestan Salamin, Nicolas Greub, Gilbert Genome Biol Evol Research Article Amoeba-resisting microorganisms raised a great interest during the last decade. Among them, some large DNA viruses present huge genomes up to 2.5 Mb long, exceeding the size of small bacterial genomes. The rate of genome evolution in terms of mutation, deletion, and gene acquisition in these genomes is yet unknown. Given the suspected high plasticity of viral genomes, the microevolution of the 346 kb genome of Lausannevirus, a member of Megavirales, was studied. Hence, Lausannevirus was co-cultured within the amoeba Acanthamoeba castellanii over one year. Despite a low number of mutations, the virus showed a genome reduction of 3.7% after 12 months. Lausannevirus genome evolution in sympatric conditions was investigated by its co-culture with Estrella lausannensis, an obligate intracellular bacterium, in the amoeba A. castellanii during one year. Cultures were split every 3 months. Genome sequencing revealed that in these conditions both, Lausannevirus and E. lausannensis, show stable genome, presenting no major rearrangement. In fact, after one year they acquired from 2 to 7 and from 4 to 10 mutations per culture for Lausannevirus and E. lausannensis, respectively. Interestingly, different mutations in the endonuclease encoding genes of Lausannevirus were observed in different subcultures, highlighting the importance of this gene product in the replication of Lausannevirus. Conversely, mutations in E. lausannensis were mainly located in a gene encoding for a phosphoenolpyruvate–protein phosphotransferase (PtsI), implicated in sugar metabolism. Moreover, in our conditions and with our analyses we detected no horizontal gene transfer during one year of co-culture. Oxford University Press 2017-05-19 /pmc/articles/PMC5513546/ /pubmed/28525571 http://dx.doi.org/10.1093/gbe/evx074 Text en © The Author(s) 2017. 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 Research Article
Mueller, Linda
Bertelli, Claire
Pillonel, Trestan
Salamin, Nicolas
Greub, Gilbert
One Year Genome Evolution of Lausannevirus in Allopatric versus Sympatric Conditions
title One Year Genome Evolution of Lausannevirus in Allopatric versus Sympatric Conditions
title_full One Year Genome Evolution of Lausannevirus in Allopatric versus Sympatric Conditions
title_fullStr One Year Genome Evolution of Lausannevirus in Allopatric versus Sympatric Conditions
title_full_unstemmed One Year Genome Evolution of Lausannevirus in Allopatric versus Sympatric Conditions
title_short One Year Genome Evolution of Lausannevirus in Allopatric versus Sympatric Conditions
title_sort one year genome evolution of lausannevirus in allopatric versus sympatric conditions
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5513546/
https://www.ncbi.nlm.nih.gov/pubmed/28525571
http://dx.doi.org/10.1093/gbe/evx074
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