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Comparative Pathogenesis, Genomics and Phylogeography of Mousepox
Ectromelia virus (ECTV), the causative agent of mousepox, has threatened laboratory mouse colonies worldwide for almost a century. Mousepox has been valuable for the understanding of poxvirus pathogenesis and immune evasion. Here, we have monitored in parallel the pathogenesis of nine ECTVs in BALB/...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8232671/ https://www.ncbi.nlm.nih.gov/pubmed/34203773 http://dx.doi.org/10.3390/v13061146 |
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author | Mavian, Carla López-Bueno, Alberto Martín, Rocío Nitsche, Andreas Alcamí, Antonio |
author_facet | Mavian, Carla López-Bueno, Alberto Martín, Rocío Nitsche, Andreas Alcamí, Antonio |
author_sort | Mavian, Carla |
collection | PubMed |
description | Ectromelia virus (ECTV), the causative agent of mousepox, has threatened laboratory mouse colonies worldwide for almost a century. Mousepox has been valuable for the understanding of poxvirus pathogenesis and immune evasion. Here, we have monitored in parallel the pathogenesis of nine ECTVs in BALB/cJ mice and report the full-length genome sequence of eight novel ECTV isolates or strains, including the first ECTV isolated from a field mouse, ECTV-MouKre. This approach allowed us to identify several genes, absent in strains attenuated through serial passages in culture, that may play a role in virulence and a set of putative genes that may be involved in enhancing viral growth in vitro. We identified a putative strong inhibitor of the host inflammatory response in ECTV-MouKre, an isolate that did not cause local foot swelling and developed a moderate virulence. Most of the ECTVs, except ECTV-Hampstead, encode a truncated version of the P4c protein that impairs the recruitment of virions into the A-type inclusion bodies, and our data suggest that P4c may play a role in viral dissemination and transmission. This is the first comprehensive report that sheds light into the phylogenetic and geographic relationship of the worldwide outbreak dynamics for the ECTV species. |
format | Online Article Text |
id | pubmed-8232671 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-82326712021-06-26 Comparative Pathogenesis, Genomics and Phylogeography of Mousepox Mavian, Carla López-Bueno, Alberto Martín, Rocío Nitsche, Andreas Alcamí, Antonio Viruses Article Ectromelia virus (ECTV), the causative agent of mousepox, has threatened laboratory mouse colonies worldwide for almost a century. Mousepox has been valuable for the understanding of poxvirus pathogenesis and immune evasion. Here, we have monitored in parallel the pathogenesis of nine ECTVs in BALB/cJ mice and report the full-length genome sequence of eight novel ECTV isolates or strains, including the first ECTV isolated from a field mouse, ECTV-MouKre. This approach allowed us to identify several genes, absent in strains attenuated through serial passages in culture, that may play a role in virulence and a set of putative genes that may be involved in enhancing viral growth in vitro. We identified a putative strong inhibitor of the host inflammatory response in ECTV-MouKre, an isolate that did not cause local foot swelling and developed a moderate virulence. Most of the ECTVs, except ECTV-Hampstead, encode a truncated version of the P4c protein that impairs the recruitment of virions into the A-type inclusion bodies, and our data suggest that P4c may play a role in viral dissemination and transmission. This is the first comprehensive report that sheds light into the phylogenetic and geographic relationship of the worldwide outbreak dynamics for the ECTV species. MDPI 2021-06-15 /pmc/articles/PMC8232671/ /pubmed/34203773 http://dx.doi.org/10.3390/v13061146 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Mavian, Carla López-Bueno, Alberto Martín, Rocío Nitsche, Andreas Alcamí, Antonio Comparative Pathogenesis, Genomics and Phylogeography of Mousepox |
title | Comparative Pathogenesis, Genomics and Phylogeography of Mousepox |
title_full | Comparative Pathogenesis, Genomics and Phylogeography of Mousepox |
title_fullStr | Comparative Pathogenesis, Genomics and Phylogeography of Mousepox |
title_full_unstemmed | Comparative Pathogenesis, Genomics and Phylogeography of Mousepox |
title_short | Comparative Pathogenesis, Genomics and Phylogeography of Mousepox |
title_sort | comparative pathogenesis, genomics and phylogeography of mousepox |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8232671/ https://www.ncbi.nlm.nih.gov/pubmed/34203773 http://dx.doi.org/10.3390/v13061146 |
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