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Emergence of Cowpox: Study of the Virulence of Clinical Strains and Evaluation of Antivirals

The last years, cowpox infections are being increasingly reported through Eurasia. Cowpox viruses (CPXVs) have been reported to have different genotypes and may be subdivided in at least five genetically distinct monophyletic clusters. However, little is known about their in vitro and in vivo featur...

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Autores principales: Duraffour, Sophie, Mertens, Barbara, Meyer, Hermann, van den Oord, Joost J., Mitera, Tania, Matthys, Patrick, Snoeck, Robert, Andrei, Graciela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3574090/
https://www.ncbi.nlm.nih.gov/pubmed/23457480
http://dx.doi.org/10.1371/journal.pone.0055808
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author Duraffour, Sophie
Mertens, Barbara
Meyer, Hermann
van den Oord, Joost J.
Mitera, Tania
Matthys, Patrick
Snoeck, Robert
Andrei, Graciela
author_facet Duraffour, Sophie
Mertens, Barbara
Meyer, Hermann
van den Oord, Joost J.
Mitera, Tania
Matthys, Patrick
Snoeck, Robert
Andrei, Graciela
author_sort Duraffour, Sophie
collection PubMed
description The last years, cowpox infections are being increasingly reported through Eurasia. Cowpox viruses (CPXVs) have been reported to have different genotypes and may be subdivided in at least five genetically distinct monophyletic clusters. However, little is known about their in vitro and in vivo features. In this report, five genetically diverse CPXVs, including one reference strain (CPXV strain Brighton) and four clinical isolates from human and animal cases, were compared with regard to growth in cells, pathogenicity in mice and inhibition by antivirals. While all CPXVs replicated similarly in vitro and showed comparable antiviral susceptibility, marked discrepancies were seen in vivo, including differences in virulence with recorded mortality rates of 0%, 20% and 100%. The four CPXV clinical isolates appeared less pathogenic than two reference strains, CPXV Brighton and vaccinia virus Western-Reserve. Disease severity seemed to correlate with high viral DNA loads in several organs, virus titers in lung tissues and levels of IL-6 cytokine in the sera. Our study highlighted that the species CPXV consists of viruses that not only differ considerably in their genotypes but also in their in vivo phenotypes, indicating that CPXVs should not be longer classified as a single species. Lung virus titers and IL-6 cytokine level in mice may be used as biomarkers for predicting disease severity. We further demonstrated the potential benefit of cidofovir, CMX001 and ST-246 use as antiviral therapy.
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spelling pubmed-35740902013-03-01 Emergence of Cowpox: Study of the Virulence of Clinical Strains and Evaluation of Antivirals Duraffour, Sophie Mertens, Barbara Meyer, Hermann van den Oord, Joost J. Mitera, Tania Matthys, Patrick Snoeck, Robert Andrei, Graciela PLoS One Research Article The last years, cowpox infections are being increasingly reported through Eurasia. Cowpox viruses (CPXVs) have been reported to have different genotypes and may be subdivided in at least five genetically distinct monophyletic clusters. However, little is known about their in vitro and in vivo features. In this report, five genetically diverse CPXVs, including one reference strain (CPXV strain Brighton) and four clinical isolates from human and animal cases, were compared with regard to growth in cells, pathogenicity in mice and inhibition by antivirals. While all CPXVs replicated similarly in vitro and showed comparable antiviral susceptibility, marked discrepancies were seen in vivo, including differences in virulence with recorded mortality rates of 0%, 20% and 100%. The four CPXV clinical isolates appeared less pathogenic than two reference strains, CPXV Brighton and vaccinia virus Western-Reserve. Disease severity seemed to correlate with high viral DNA loads in several organs, virus titers in lung tissues and levels of IL-6 cytokine in the sera. Our study highlighted that the species CPXV consists of viruses that not only differ considerably in their genotypes but also in their in vivo phenotypes, indicating that CPXVs should not be longer classified as a single species. Lung virus titers and IL-6 cytokine level in mice may be used as biomarkers for predicting disease severity. We further demonstrated the potential benefit of cidofovir, CMX001 and ST-246 use as antiviral therapy. Public Library of Science 2013-02-15 /pmc/articles/PMC3574090/ /pubmed/23457480 http://dx.doi.org/10.1371/journal.pone.0055808 Text en © 2013 Duraffour et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Duraffour, Sophie
Mertens, Barbara
Meyer, Hermann
van den Oord, Joost J.
Mitera, Tania
Matthys, Patrick
Snoeck, Robert
Andrei, Graciela
Emergence of Cowpox: Study of the Virulence of Clinical Strains and Evaluation of Antivirals
title Emergence of Cowpox: Study of the Virulence of Clinical Strains and Evaluation of Antivirals
title_full Emergence of Cowpox: Study of the Virulence of Clinical Strains and Evaluation of Antivirals
title_fullStr Emergence of Cowpox: Study of the Virulence of Clinical Strains and Evaluation of Antivirals
title_full_unstemmed Emergence of Cowpox: Study of the Virulence of Clinical Strains and Evaluation of Antivirals
title_short Emergence of Cowpox: Study of the Virulence of Clinical Strains and Evaluation of Antivirals
title_sort emergence of cowpox: study of the virulence of clinical strains and evaluation of antivirals
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3574090/
https://www.ncbi.nlm.nih.gov/pubmed/23457480
http://dx.doi.org/10.1371/journal.pone.0055808
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