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Laboratory Infection of Novel Akhmeta Virus in CAST/EiJ Mice
Akhmeta virus is a zoonotic Orthopoxvirus first identified in 2013 in the country of Georgia. Subsequent ecological investigations in Georgia have found evidence that this virus is widespread in its geographic distribution within the country and in its host-range, with rodents likely involved in its...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7763702/ https://www.ncbi.nlm.nih.gov/pubmed/33317132 http://dx.doi.org/10.3390/v12121416 |
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author | Morgan, Clint N. Matheny, Audrey M. Nakazawa, Yoshinori J. Kling, Chantal Gallardo-Romero, Nadia Seigler, Laurie Barbosa Costa, Galileu Hutson, Christina Maghlakelidze, Giorgi Olson, Victoria Doty, Jeffrey B. |
author_facet | Morgan, Clint N. Matheny, Audrey M. Nakazawa, Yoshinori J. Kling, Chantal Gallardo-Romero, Nadia Seigler, Laurie Barbosa Costa, Galileu Hutson, Christina Maghlakelidze, Giorgi Olson, Victoria Doty, Jeffrey B. |
author_sort | Morgan, Clint N. |
collection | PubMed |
description | Akhmeta virus is a zoonotic Orthopoxvirus first identified in 2013 in the country of Georgia. Subsequent ecological investigations in Georgia have found evidence that this virus is widespread in its geographic distribution within the country and in its host-range, with rodents likely involved in its circulation in the wild. Yet, little is known about the pathogenicity of this virus in rodents. We conducted the first laboratory infection of Akhmeta virus in CAST/EiJ Mus musculus to further characterize this novel virus. We found a dose-dependent effect on mortality and weight loss (p < 0.05). Anti-orthopoxvirus antibodies were detected in the second- and third-highest dose groups (5 × 10(4) pfu and 3 × 10(2) pfu) at euthanasia by day 10, and day 14 post-infection, respectively. Anti-orthopoxvirus antibodies were not detected in the highest dose group (3 × 10(6) pfu), which were euthanized at day 7 post-infection and had high viral load in tissues, suggesting they succumbed to disease prior to mounting an effective immune response. In order of highest burden, viable virus was detected in the nostril, lung, tail, liver and spleen. All individuals tested in the highest dose groups were DNAemic. Akhmeta virus was highly pathogenic in CAST/EiJ Mus musculus, causing 100% mortality when ≥3 × 10(2) pfu was administered. |
format | Online Article Text |
id | pubmed-7763702 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-77637022020-12-27 Laboratory Infection of Novel Akhmeta Virus in CAST/EiJ Mice Morgan, Clint N. Matheny, Audrey M. Nakazawa, Yoshinori J. Kling, Chantal Gallardo-Romero, Nadia Seigler, Laurie Barbosa Costa, Galileu Hutson, Christina Maghlakelidze, Giorgi Olson, Victoria Doty, Jeffrey B. Viruses Article Akhmeta virus is a zoonotic Orthopoxvirus first identified in 2013 in the country of Georgia. Subsequent ecological investigations in Georgia have found evidence that this virus is widespread in its geographic distribution within the country and in its host-range, with rodents likely involved in its circulation in the wild. Yet, little is known about the pathogenicity of this virus in rodents. We conducted the first laboratory infection of Akhmeta virus in CAST/EiJ Mus musculus to further characterize this novel virus. We found a dose-dependent effect on mortality and weight loss (p < 0.05). Anti-orthopoxvirus antibodies were detected in the second- and third-highest dose groups (5 × 10(4) pfu and 3 × 10(2) pfu) at euthanasia by day 10, and day 14 post-infection, respectively. Anti-orthopoxvirus antibodies were not detected in the highest dose group (3 × 10(6) pfu), which were euthanized at day 7 post-infection and had high viral load in tissues, suggesting they succumbed to disease prior to mounting an effective immune response. In order of highest burden, viable virus was detected in the nostril, lung, tail, liver and spleen. All individuals tested in the highest dose groups were DNAemic. Akhmeta virus was highly pathogenic in CAST/EiJ Mus musculus, causing 100% mortality when ≥3 × 10(2) pfu was administered. MDPI 2020-12-09 /pmc/articles/PMC7763702/ /pubmed/33317132 http://dx.doi.org/10.3390/v12121416 Text en © 2020 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 | Article Morgan, Clint N. Matheny, Audrey M. Nakazawa, Yoshinori J. Kling, Chantal Gallardo-Romero, Nadia Seigler, Laurie Barbosa Costa, Galileu Hutson, Christina Maghlakelidze, Giorgi Olson, Victoria Doty, Jeffrey B. Laboratory Infection of Novel Akhmeta Virus in CAST/EiJ Mice |
title | Laboratory Infection of Novel Akhmeta Virus in CAST/EiJ Mice |
title_full | Laboratory Infection of Novel Akhmeta Virus in CAST/EiJ Mice |
title_fullStr | Laboratory Infection of Novel Akhmeta Virus in CAST/EiJ Mice |
title_full_unstemmed | Laboratory Infection of Novel Akhmeta Virus in CAST/EiJ Mice |
title_short | Laboratory Infection of Novel Akhmeta Virus in CAST/EiJ Mice |
title_sort | laboratory infection of novel akhmeta virus in cast/eij mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7763702/ https://www.ncbi.nlm.nih.gov/pubmed/33317132 http://dx.doi.org/10.3390/v12121416 |
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