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Single-cell mutation rate of turnip crinkle virus (-)-strand replication intermediates
Viruses with single-stranded, positive-sense (+) RNA genomes incur high numbers of errors during replication, thereby creating diversified genome populations from which new, better adapted viral variants can emerge. However, a definitive error rate is known for a relatively few (+) RNA plant viruses...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10449226/ https://www.ncbi.nlm.nih.gov/pubmed/37578959 http://dx.doi.org/10.1371/journal.ppat.1011395 |
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author | Carvalho, Camila Perdoncini Han, Junping Khemsom, Khwannarin Ren, Ruifan Camargo, Luis Eduardo Aranha Miyashita, Shuhei Qu, Feng |
author_facet | Carvalho, Camila Perdoncini Han, Junping Khemsom, Khwannarin Ren, Ruifan Camargo, Luis Eduardo Aranha Miyashita, Shuhei Qu, Feng |
author_sort | Carvalho, Camila Perdoncini |
collection | PubMed |
description | Viruses with single-stranded, positive-sense (+) RNA genomes incur high numbers of errors during replication, thereby creating diversified genome populations from which new, better adapted viral variants can emerge. However, a definitive error rate is known for a relatively few (+) RNA plant viruses, due to challenges to account for perturbations caused by natural selection and/or experimental set-ups. To address these challenges, we developed a new approach that exclusively profiled errors in the (-)-strand replication intermediates of turnip crinkle virus (TCV), in singly infected cells. A series of controls and safeguards were devised to ensure errors inherent to the experimental process were accounted for. This approach permitted the estimation of a TCV error rate of 8.47 X 10(−5) substitution per nucleotide site per cell infection. Importantly, the characteristic error distribution pattern among the 50 copies of 2,363-base-pair cDNA fragments predicted that nearly all TCV (-) strands were products of one replication cycle per cell. Furthermore, some of the errors probably elevated error frequencies by lowering the fidelity of TCV RNA-dependent RNA polymerase, and/or permitting occasional re-replication of progeny genomes. In summary, by profiling errors in TCV (-)-strand intermediates incurred during replication in single cells, this study provided strong support for a stamping machine mode of replication employed by a (+) RNA virus. |
format | Online Article Text |
id | pubmed-10449226 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-104492262023-08-25 Single-cell mutation rate of turnip crinkle virus (-)-strand replication intermediates Carvalho, Camila Perdoncini Han, Junping Khemsom, Khwannarin Ren, Ruifan Camargo, Luis Eduardo Aranha Miyashita, Shuhei Qu, Feng PLoS Pathog Research Article Viruses with single-stranded, positive-sense (+) RNA genomes incur high numbers of errors during replication, thereby creating diversified genome populations from which new, better adapted viral variants can emerge. However, a definitive error rate is known for a relatively few (+) RNA plant viruses, due to challenges to account for perturbations caused by natural selection and/or experimental set-ups. To address these challenges, we developed a new approach that exclusively profiled errors in the (-)-strand replication intermediates of turnip crinkle virus (TCV), in singly infected cells. A series of controls and safeguards were devised to ensure errors inherent to the experimental process were accounted for. This approach permitted the estimation of a TCV error rate of 8.47 X 10(−5) substitution per nucleotide site per cell infection. Importantly, the characteristic error distribution pattern among the 50 copies of 2,363-base-pair cDNA fragments predicted that nearly all TCV (-) strands were products of one replication cycle per cell. Furthermore, some of the errors probably elevated error frequencies by lowering the fidelity of TCV RNA-dependent RNA polymerase, and/or permitting occasional re-replication of progeny genomes. In summary, by profiling errors in TCV (-)-strand intermediates incurred during replication in single cells, this study provided strong support for a stamping machine mode of replication employed by a (+) RNA virus. Public Library of Science 2023-08-14 /pmc/articles/PMC10449226/ /pubmed/37578959 http://dx.doi.org/10.1371/journal.ppat.1011395 Text en © 2023 Carvalho et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Carvalho, Camila Perdoncini Han, Junping Khemsom, Khwannarin Ren, Ruifan Camargo, Luis Eduardo Aranha Miyashita, Shuhei Qu, Feng Single-cell mutation rate of turnip crinkle virus (-)-strand replication intermediates |
title | Single-cell mutation rate of turnip crinkle virus (-)-strand replication intermediates |
title_full | Single-cell mutation rate of turnip crinkle virus (-)-strand replication intermediates |
title_fullStr | Single-cell mutation rate of turnip crinkle virus (-)-strand replication intermediates |
title_full_unstemmed | Single-cell mutation rate of turnip crinkle virus (-)-strand replication intermediates |
title_short | Single-cell mutation rate of turnip crinkle virus (-)-strand replication intermediates |
title_sort | single-cell mutation rate of turnip crinkle virus (-)-strand replication intermediates |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10449226/ https://www.ncbi.nlm.nih.gov/pubmed/37578959 http://dx.doi.org/10.1371/journal.ppat.1011395 |
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