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Natural history of nonhuman primates after conjunctival exposure to Ebola virus

Transmission of Ebola virus (EBOV) primarily occurs via contact exposure of mucosal surfaces with infected body fluids. Historically, nonhuman primate (NHP) challenge studies have employed intramuscular (i.m.) or small particle aerosol exposure, which are largely lethal routes of infection, but mimi...

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Autores principales: Cross, Robert W., Prasad, Abhishek N., Woolsey, Courtney B., Agans, Krystle N., Borisevich, Viktoriya, Dobias, Natalie S., Comer, Jason E., Deer, Daniel J., Geisbert, Joan B., Rasmussen, Angela L., Lipkin, Walter Ian, Fenton, Karla A., Geisbert, Thomas W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10011569/
https://www.ncbi.nlm.nih.gov/pubmed/36914721
http://dx.doi.org/10.1038/s41598-023-31027-7
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author Cross, Robert W.
Prasad, Abhishek N.
Woolsey, Courtney B.
Agans, Krystle N.
Borisevich, Viktoriya
Dobias, Natalie S.
Comer, Jason E.
Deer, Daniel J.
Geisbert, Joan B.
Rasmussen, Angela L.
Lipkin, Walter Ian
Fenton, Karla A.
Geisbert, Thomas W.
author_facet Cross, Robert W.
Prasad, Abhishek N.
Woolsey, Courtney B.
Agans, Krystle N.
Borisevich, Viktoriya
Dobias, Natalie S.
Comer, Jason E.
Deer, Daniel J.
Geisbert, Joan B.
Rasmussen, Angela L.
Lipkin, Walter Ian
Fenton, Karla A.
Geisbert, Thomas W.
author_sort Cross, Robert W.
collection PubMed
description Transmission of Ebola virus (EBOV) primarily occurs via contact exposure of mucosal surfaces with infected body fluids. Historically, nonhuman primate (NHP) challenge studies have employed intramuscular (i.m.) or small particle aerosol exposure, which are largely lethal routes of infection, but mimic worst-case scenarios such as a needlestick or intentional release, respectively. When exposed by more likely routes of natural infection, limited NHP studies have shown delayed onset of disease and reduced mortality. Here, we performed a series of systematic natural history studies in cynomolgus macaques with a range of conjunctival exposure doses. Challenge with 10,000 plaque forming units (PFU) of EBOV was uniformly lethal, whereas 5/6 subjects survived lower dose challenges (100 or 500 PFU). Conjunctival challenge resulted in a protracted time-to death compared to i.m. Asymptomatic infection was observed in survivors with limited detection of EBOV replication. Inconsistent seropositivity in survivors may suggest physical or natural immunological barriers are sufficient to prevent widespread viral dissemination.
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spelling pubmed-100115692023-03-15 Natural history of nonhuman primates after conjunctival exposure to Ebola virus Cross, Robert W. Prasad, Abhishek N. Woolsey, Courtney B. Agans, Krystle N. Borisevich, Viktoriya Dobias, Natalie S. Comer, Jason E. Deer, Daniel J. Geisbert, Joan B. Rasmussen, Angela L. Lipkin, Walter Ian Fenton, Karla A. Geisbert, Thomas W. Sci Rep Article Transmission of Ebola virus (EBOV) primarily occurs via contact exposure of mucosal surfaces with infected body fluids. Historically, nonhuman primate (NHP) challenge studies have employed intramuscular (i.m.) or small particle aerosol exposure, which are largely lethal routes of infection, but mimic worst-case scenarios such as a needlestick or intentional release, respectively. When exposed by more likely routes of natural infection, limited NHP studies have shown delayed onset of disease and reduced mortality. Here, we performed a series of systematic natural history studies in cynomolgus macaques with a range of conjunctival exposure doses. Challenge with 10,000 plaque forming units (PFU) of EBOV was uniformly lethal, whereas 5/6 subjects survived lower dose challenges (100 or 500 PFU). Conjunctival challenge resulted in a protracted time-to death compared to i.m. Asymptomatic infection was observed in survivors with limited detection of EBOV replication. Inconsistent seropositivity in survivors may suggest physical or natural immunological barriers are sufficient to prevent widespread viral dissemination. Nature Publishing Group UK 2023-03-13 /pmc/articles/PMC10011569/ /pubmed/36914721 http://dx.doi.org/10.1038/s41598-023-31027-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Cross, Robert W.
Prasad, Abhishek N.
Woolsey, Courtney B.
Agans, Krystle N.
Borisevich, Viktoriya
Dobias, Natalie S.
Comer, Jason E.
Deer, Daniel J.
Geisbert, Joan B.
Rasmussen, Angela L.
Lipkin, Walter Ian
Fenton, Karla A.
Geisbert, Thomas W.
Natural history of nonhuman primates after conjunctival exposure to Ebola virus
title Natural history of nonhuman primates after conjunctival exposure to Ebola virus
title_full Natural history of nonhuman primates after conjunctival exposure to Ebola virus
title_fullStr Natural history of nonhuman primates after conjunctival exposure to Ebola virus
title_full_unstemmed Natural history of nonhuman primates after conjunctival exposure to Ebola virus
title_short Natural history of nonhuman primates after conjunctival exposure to Ebola virus
title_sort natural history of nonhuman primates after conjunctival exposure to ebola virus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10011569/
https://www.ncbi.nlm.nih.gov/pubmed/36914721
http://dx.doi.org/10.1038/s41598-023-31027-7
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