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Natural History of Aerosol Induced Lassa Fever in Non-Human Primates
Lassa virus (LASV), an arenavirus causing Lassa fever, is endemic to West Africa with up to 300,000 cases and between 5000 and 10,000 deaths per year. Rarely seen in the United States, Lassa virus is a CDC category A biological agent inasmuch deliberate aerosol exposure can have high mortality rates...
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/PMC7354473/ https://www.ncbi.nlm.nih.gov/pubmed/32485952 http://dx.doi.org/10.3390/v12060593 |
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author | Downs, Isaac L. Shaia, Carl I. Zeng, Xiankun Johnson, Joshua C. Hensley, Lisa Saunders, David L. Rossi, Franco Cashman, Kathleen A. Esham, Heather L. Gregory, Melissa K. Pratt, William D. Trefry, John C. Everson, Kyle A. Larcom, Charles B. Okwesili, Arthur C. Cardile, Anthony P. Honko, Anna |
author_facet | Downs, Isaac L. Shaia, Carl I. Zeng, Xiankun Johnson, Joshua C. Hensley, Lisa Saunders, David L. Rossi, Franco Cashman, Kathleen A. Esham, Heather L. Gregory, Melissa K. Pratt, William D. Trefry, John C. Everson, Kyle A. Larcom, Charles B. Okwesili, Arthur C. Cardile, Anthony P. Honko, Anna |
author_sort | Downs, Isaac L. |
collection | PubMed |
description | Lassa virus (LASV), an arenavirus causing Lassa fever, is endemic to West Africa with up to 300,000 cases and between 5000 and 10,000 deaths per year. Rarely seen in the United States, Lassa virus is a CDC category A biological agent inasmuch deliberate aerosol exposure can have high mortality rates compared to naturally acquired infection. With the need for an animal model, specific countermeasures remain elusive as there is no FDA-approved vaccine. This natural history of aerosolized Lassa virus exposure in Macaca fascicularis was studied under continuous telemetric surveillance. The macaque response to challenge was largely analogous to severe human disease with fever, tachycardia, hypotension, and tachypnea. During initial observations, an increase trend of activated monocytes positive for viral glycoprotein was accompanied by lymphocytopenia. Disease uniformly progressed to high viremia followed by low anion gap, alkalosis, anemia, and thrombocytopenia. Hypoproteinemia occurred late in infection followed by increased levels of white blood cells, cytokines, chemokines, and biochemical markers of liver injury. Viral nucleic acids were detected in tissues of three non-survivors at endpoint, but not in the lone survivor. This study provides useful details to benchmark a pivotal model of Lassa fever in support of medical countermeasure development for both endemic disease and traditional biodefense purposes. |
format | Online Article Text |
id | pubmed-7354473 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-73544732020-08-05 Natural History of Aerosol Induced Lassa Fever in Non-Human Primates Downs, Isaac L. Shaia, Carl I. Zeng, Xiankun Johnson, Joshua C. Hensley, Lisa Saunders, David L. Rossi, Franco Cashman, Kathleen A. Esham, Heather L. Gregory, Melissa K. Pratt, William D. Trefry, John C. Everson, Kyle A. Larcom, Charles B. Okwesili, Arthur C. Cardile, Anthony P. Honko, Anna Viruses Article Lassa virus (LASV), an arenavirus causing Lassa fever, is endemic to West Africa with up to 300,000 cases and between 5000 and 10,000 deaths per year. Rarely seen in the United States, Lassa virus is a CDC category A biological agent inasmuch deliberate aerosol exposure can have high mortality rates compared to naturally acquired infection. With the need for an animal model, specific countermeasures remain elusive as there is no FDA-approved vaccine. This natural history of aerosolized Lassa virus exposure in Macaca fascicularis was studied under continuous telemetric surveillance. The macaque response to challenge was largely analogous to severe human disease with fever, tachycardia, hypotension, and tachypnea. During initial observations, an increase trend of activated monocytes positive for viral glycoprotein was accompanied by lymphocytopenia. Disease uniformly progressed to high viremia followed by low anion gap, alkalosis, anemia, and thrombocytopenia. Hypoproteinemia occurred late in infection followed by increased levels of white blood cells, cytokines, chemokines, and biochemical markers of liver injury. Viral nucleic acids were detected in tissues of three non-survivors at endpoint, but not in the lone survivor. This study provides useful details to benchmark a pivotal model of Lassa fever in support of medical countermeasure development for both endemic disease and traditional biodefense purposes. MDPI 2020-05-29 /pmc/articles/PMC7354473/ /pubmed/32485952 http://dx.doi.org/10.3390/v12060593 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 Downs, Isaac L. Shaia, Carl I. Zeng, Xiankun Johnson, Joshua C. Hensley, Lisa Saunders, David L. Rossi, Franco Cashman, Kathleen A. Esham, Heather L. Gregory, Melissa K. Pratt, William D. Trefry, John C. Everson, Kyle A. Larcom, Charles B. Okwesili, Arthur C. Cardile, Anthony P. Honko, Anna Natural History of Aerosol Induced Lassa Fever in Non-Human Primates |
title | Natural History of Aerosol Induced Lassa Fever in Non-Human Primates |
title_full | Natural History of Aerosol Induced Lassa Fever in Non-Human Primates |
title_fullStr | Natural History of Aerosol Induced Lassa Fever in Non-Human Primates |
title_full_unstemmed | Natural History of Aerosol Induced Lassa Fever in Non-Human Primates |
title_short | Natural History of Aerosol Induced Lassa Fever in Non-Human Primates |
title_sort | natural history of aerosol induced lassa fever in non-human primates |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7354473/ https://www.ncbi.nlm.nih.gov/pubmed/32485952 http://dx.doi.org/10.3390/v12060593 |
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