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Rates of Vaccine Evolution Show Strong Effects of Latency: Implications for Varicella Zoster Virus Epidemiology
Varicella-zoster virus (VZV) causes chickenpox and shingles, and is found in human populations worldwide. The lack of temporal signal in the diversity of VZV makes substitution rate estimates unreliable, which is a barrier to understanding the context of its global spread. Here, we estimate rates of...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4379407/ https://www.ncbi.nlm.nih.gov/pubmed/25568346 http://dx.doi.org/10.1093/molbev/msu406 |
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author | Weinert, Lucy A. Depledge, Daniel P. Kundu, Samit Gershon, Anne A. Nichols, Richard A. Balloux, Francois Welch, John J. Breuer, Judith |
author_facet | Weinert, Lucy A. Depledge, Daniel P. Kundu, Samit Gershon, Anne A. Nichols, Richard A. Balloux, Francois Welch, John J. Breuer, Judith |
author_sort | Weinert, Lucy A. |
collection | PubMed |
description | Varicella-zoster virus (VZV) causes chickenpox and shingles, and is found in human populations worldwide. The lack of temporal signal in the diversity of VZV makes substitution rate estimates unreliable, which is a barrier to understanding the context of its global spread. Here, we estimate rates of evolution by studying live attenuated vaccines, which evolved in 22 vaccinated patients for known periods of time, sometimes, but not always undergoing latency. We show that the attenuated virus evolves rapidly (∼10(−6) substitutions/site/day), but that rates decrease dramatically when the virus undergoes latency. These data are best explained by a model in which viral populations evolve for around 13 days before becoming latent, but then undergo no replication during latency. This implies that rates of viral evolution will depend strongly on transmission patterns. Nevertheless, we show that implausibly long latency periods are required to date the most recent common ancestor of extant VZV to an “out-of-Africa” migration with humans, as has been previously suggested. |
format | Online Article Text |
id | pubmed-4379407 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-43794072015-04-15 Rates of Vaccine Evolution Show Strong Effects of Latency: Implications for Varicella Zoster Virus Epidemiology Weinert, Lucy A. Depledge, Daniel P. Kundu, Samit Gershon, Anne A. Nichols, Richard A. Balloux, Francois Welch, John J. Breuer, Judith Mol Biol Evol Discoveries Varicella-zoster virus (VZV) causes chickenpox and shingles, and is found in human populations worldwide. The lack of temporal signal in the diversity of VZV makes substitution rate estimates unreliable, which is a barrier to understanding the context of its global spread. Here, we estimate rates of evolution by studying live attenuated vaccines, which evolved in 22 vaccinated patients for known periods of time, sometimes, but not always undergoing latency. We show that the attenuated virus evolves rapidly (∼10(−6) substitutions/site/day), but that rates decrease dramatically when the virus undergoes latency. These data are best explained by a model in which viral populations evolve for around 13 days before becoming latent, but then undergo no replication during latency. This implies that rates of viral evolution will depend strongly on transmission patterns. Nevertheless, we show that implausibly long latency periods are required to date the most recent common ancestor of extant VZV to an “out-of-Africa” migration with humans, as has been previously suggested. Oxford University Press 2015-04 2015-01-06 /pmc/articles/PMC4379407/ /pubmed/25568346 http://dx.doi.org/10.1093/molbev/msu406 Text en © The Author 2015. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Discoveries Weinert, Lucy A. Depledge, Daniel P. Kundu, Samit Gershon, Anne A. Nichols, Richard A. Balloux, Francois Welch, John J. Breuer, Judith Rates of Vaccine Evolution Show Strong Effects of Latency: Implications for Varicella Zoster Virus Epidemiology |
title | Rates of Vaccine Evolution Show Strong Effects of Latency: Implications for Varicella Zoster Virus Epidemiology |
title_full | Rates of Vaccine Evolution Show Strong Effects of Latency: Implications for Varicella Zoster Virus Epidemiology |
title_fullStr | Rates of Vaccine Evolution Show Strong Effects of Latency: Implications for Varicella Zoster Virus Epidemiology |
title_full_unstemmed | Rates of Vaccine Evolution Show Strong Effects of Latency: Implications for Varicella Zoster Virus Epidemiology |
title_short | Rates of Vaccine Evolution Show Strong Effects of Latency: Implications for Varicella Zoster Virus Epidemiology |
title_sort | rates of vaccine evolution show strong effects of latency: implications for varicella zoster virus epidemiology |
topic | Discoveries |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4379407/ https://www.ncbi.nlm.nih.gov/pubmed/25568346 http://dx.doi.org/10.1093/molbev/msu406 |
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