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Comment: Characterization of Two Historic Smallpox Specimens from a Czech Museum

The complete genome sequences of two strains of variola virus (VARV) sampled from human smallpox specimens present in the Czech National Museum, Prague, were recently determined, with one of the sequences estimated to date to the mid-19th century. Using molecular clock methods, the authors of this s...

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Autores principales: Porter, Ashleigh F., Duggan, Ana T., Poinar, Hendrik N., Holmes, Edward C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5691628/
https://www.ncbi.nlm.nih.gov/pubmed/28956829
http://dx.doi.org/10.3390/v9100276
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author Porter, Ashleigh F.
Duggan, Ana T.
Poinar, Hendrik N.
Holmes, Edward C.
author_facet Porter, Ashleigh F.
Duggan, Ana T.
Poinar, Hendrik N.
Holmes, Edward C.
author_sort Porter, Ashleigh F.
collection PubMed
description The complete genome sequences of two strains of variola virus (VARV) sampled from human smallpox specimens present in the Czech National Museum, Prague, were recently determined, with one of the sequences estimated to date to the mid-19th century. Using molecular clock methods, the authors of this study go on to infer that the currently available strains of VARV share an older common ancestor, at around 1350 AD, than some recent estimates based on other archival human samples. Herein, we show that the two Czech strains exhibit anomalous branch lengths given their proposed age, and by assuming a constant rate of evolutionary change across the rest of the VARV phylogeny estimate that their true age in fact lies between 1918 and 1937. We therefore suggest that the age of the common ancestor of currently available VARV genomes most likely dates to late 16th and early 17th centuries and not ~1350 AD.
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spelling pubmed-56916282017-11-22 Comment: Characterization of Two Historic Smallpox Specimens from a Czech Museum Porter, Ashleigh F. Duggan, Ana T. Poinar, Hendrik N. Holmes, Edward C. Viruses Comment The complete genome sequences of two strains of variola virus (VARV) sampled from human smallpox specimens present in the Czech National Museum, Prague, were recently determined, with one of the sequences estimated to date to the mid-19th century. Using molecular clock methods, the authors of this study go on to infer that the currently available strains of VARV share an older common ancestor, at around 1350 AD, than some recent estimates based on other archival human samples. Herein, we show that the two Czech strains exhibit anomalous branch lengths given their proposed age, and by assuming a constant rate of evolutionary change across the rest of the VARV phylogeny estimate that their true age in fact lies between 1918 and 1937. We therefore suggest that the age of the common ancestor of currently available VARV genomes most likely dates to late 16th and early 17th centuries and not ~1350 AD. MDPI 2017-09-28 /pmc/articles/PMC5691628/ /pubmed/28956829 http://dx.doi.org/10.3390/v9100276 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Comment
Porter, Ashleigh F.
Duggan, Ana T.
Poinar, Hendrik N.
Holmes, Edward C.
Comment: Characterization of Two Historic Smallpox Specimens from a Czech Museum
title Comment: Characterization of Two Historic Smallpox Specimens from a Czech Museum
title_full Comment: Characterization of Two Historic Smallpox Specimens from a Czech Museum
title_fullStr Comment: Characterization of Two Historic Smallpox Specimens from a Czech Museum
title_full_unstemmed Comment: Characterization of Two Historic Smallpox Specimens from a Czech Museum
title_short Comment: Characterization of Two Historic Smallpox Specimens from a Czech Museum
title_sort comment: characterization of two historic smallpox specimens from a czech museum
topic Comment
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5691628/
https://www.ncbi.nlm.nih.gov/pubmed/28956829
http://dx.doi.org/10.3390/v9100276
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