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Dose Response of MARV/Angola Infection in Cynomolgus Macaques following IM or Aerosol Exposure
Marburg virus infection in humans causes a hemorrhagic disease with a high case fatality rate. Countermeasure development requires the use of well-characterized animal models that mimic human disease. To further characterize the cynomolgus macaque model of MARV/Angola, two independent dose response...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4586374/ https://www.ncbi.nlm.nih.gov/pubmed/26413900 http://dx.doi.org/10.1371/journal.pone.0138843 |
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author | Johnston, Sara C. Lin, Kenny L. Twenhafel, Nancy A. Raymond, Jo Lynne W. Shamblin, Joshua D. Wollen, Suzanne E. Wlazlowski, Carly B. Wilkinson, Eric R. Botto, Miriam A. Goff, Arthur J. |
author_facet | Johnston, Sara C. Lin, Kenny L. Twenhafel, Nancy A. Raymond, Jo Lynne W. Shamblin, Joshua D. Wollen, Suzanne E. Wlazlowski, Carly B. Wilkinson, Eric R. Botto, Miriam A. Goff, Arthur J. |
author_sort | Johnston, Sara C. |
collection | PubMed |
description | Marburg virus infection in humans causes a hemorrhagic disease with a high case fatality rate. Countermeasure development requires the use of well-characterized animal models that mimic human disease. To further characterize the cynomolgus macaque model of MARV/Angola, two independent dose response studies were performed using the intramuscular or aerosol routes of exposure. All animals succumbed at the lowest target dose; therefore, a dose effect could not be determined. For intramuscular-exposed animals, 100 PFU was the first target dose that was not significantly different than higher target doses in terms of time to disposition, clinical pathology, and histopathology. Although a significant difference was not observed between aerosol-exposed animals in the 10 PFU and 100 PFU target dose groups, 100 PFU was determined to be the lowest target dose that could be consistently obtained and accurately titrated in aerosol studies. |
format | Online Article Text |
id | pubmed-4586374 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-45863742015-10-01 Dose Response of MARV/Angola Infection in Cynomolgus Macaques following IM or Aerosol Exposure Johnston, Sara C. Lin, Kenny L. Twenhafel, Nancy A. Raymond, Jo Lynne W. Shamblin, Joshua D. Wollen, Suzanne E. Wlazlowski, Carly B. Wilkinson, Eric R. Botto, Miriam A. Goff, Arthur J. PLoS One Research Article Marburg virus infection in humans causes a hemorrhagic disease with a high case fatality rate. Countermeasure development requires the use of well-characterized animal models that mimic human disease. To further characterize the cynomolgus macaque model of MARV/Angola, two independent dose response studies were performed using the intramuscular or aerosol routes of exposure. All animals succumbed at the lowest target dose; therefore, a dose effect could not be determined. For intramuscular-exposed animals, 100 PFU was the first target dose that was not significantly different than higher target doses in terms of time to disposition, clinical pathology, and histopathology. Although a significant difference was not observed between aerosol-exposed animals in the 10 PFU and 100 PFU target dose groups, 100 PFU was determined to be the lowest target dose that could be consistently obtained and accurately titrated in aerosol studies. Public Library of Science 2015-09-28 /pmc/articles/PMC4586374/ /pubmed/26413900 http://dx.doi.org/10.1371/journal.pone.0138843 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. |
spellingShingle | Research Article Johnston, Sara C. Lin, Kenny L. Twenhafel, Nancy A. Raymond, Jo Lynne W. Shamblin, Joshua D. Wollen, Suzanne E. Wlazlowski, Carly B. Wilkinson, Eric R. Botto, Miriam A. Goff, Arthur J. Dose Response of MARV/Angola Infection in Cynomolgus Macaques following IM or Aerosol Exposure |
title | Dose Response of MARV/Angola Infection in Cynomolgus Macaques following IM or Aerosol Exposure |
title_full | Dose Response of MARV/Angola Infection in Cynomolgus Macaques following IM or Aerosol Exposure |
title_fullStr | Dose Response of MARV/Angola Infection in Cynomolgus Macaques following IM or Aerosol Exposure |
title_full_unstemmed | Dose Response of MARV/Angola Infection in Cynomolgus Macaques following IM or Aerosol Exposure |
title_short | Dose Response of MARV/Angola Infection in Cynomolgus Macaques following IM or Aerosol Exposure |
title_sort | dose response of marv/angola infection in cynomolgus macaques following im or aerosol exposure |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4586374/ https://www.ncbi.nlm.nih.gov/pubmed/26413900 http://dx.doi.org/10.1371/journal.pone.0138843 |
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