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Kyasanur Forest disease virus non-mouse animal models: a pilot study
OBJECTIVES: Mouse models have delivered variable recapitulation of Kyasanur Forest disease (KFD) pathology and consistently demonstrated neurological involvement which may be a limited feature of human disease. With the purpose of more accurately modelling human disease progression we infected sever...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7296627/ https://www.ncbi.nlm.nih.gov/pubmed/32539799 http://dx.doi.org/10.1186/s13104-020-05137-8 |
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author | Nikiforuk, A. M. Tierny, K. Cutts, T. A. Kobasa, D. K. Theriault, S. S. Cook, B. W. M. |
author_facet | Nikiforuk, A. M. Tierny, K. Cutts, T. A. Kobasa, D. K. Theriault, S. S. Cook, B. W. M. |
author_sort | Nikiforuk, A. M. |
collection | PubMed |
description | OBJECTIVES: Mouse models have delivered variable recapitulation of Kyasanur Forest disease (KFD) pathology and consistently demonstrated neurological involvement which may be a limited feature of human disease. With the purpose of more accurately modelling human disease progression we infected several small-mammalian models: guinea pigs, hamsters and ferrets with a titered infectious dose of Kyasanur Forest disease virus (KFDV). Clinical indicators of disease severity were observed for seventeen days, on day eighteen a visual post-mortem analysis of visceral organs was conducted. Viral load in selected tissues was measured to infer disease signs and the establishment of viral replication. DATA DESCRIPTION: Daily monitoring did not reveal any observable signs of illness; weight loss was minimal across species and gross pathology did not indicate severe viral infection. Tissue specific tropism and establishment of viral infection was monitored by quantitative real-time polymerase chain reaction (qRT-PCR). No viral replication was detected in ferrets (n = 0/3), but was present in the spleen of guinea pigs (n = 3/3) and the brain of hamsters (n = 3/3). Low levels of viral RNA were detected in multiple hamster tissues (kidney, liver, lung and spleen) suggesting the possibility of viral tropism and possible adaptation to the host. No serological tests were performed. |
format | Online Article Text |
id | pubmed-7296627 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-72966272020-06-16 Kyasanur Forest disease virus non-mouse animal models: a pilot study Nikiforuk, A. M. Tierny, K. Cutts, T. A. Kobasa, D. K. Theriault, S. S. Cook, B. W. M. BMC Res Notes Data Note OBJECTIVES: Mouse models have delivered variable recapitulation of Kyasanur Forest disease (KFD) pathology and consistently demonstrated neurological involvement which may be a limited feature of human disease. With the purpose of more accurately modelling human disease progression we infected several small-mammalian models: guinea pigs, hamsters and ferrets with a titered infectious dose of Kyasanur Forest disease virus (KFDV). Clinical indicators of disease severity were observed for seventeen days, on day eighteen a visual post-mortem analysis of visceral organs was conducted. Viral load in selected tissues was measured to infer disease signs and the establishment of viral replication. DATA DESCRIPTION: Daily monitoring did not reveal any observable signs of illness; weight loss was minimal across species and gross pathology did not indicate severe viral infection. Tissue specific tropism and establishment of viral infection was monitored by quantitative real-time polymerase chain reaction (qRT-PCR). No viral replication was detected in ferrets (n = 0/3), but was present in the spleen of guinea pigs (n = 3/3) and the brain of hamsters (n = 3/3). Low levels of viral RNA were detected in multiple hamster tissues (kidney, liver, lung and spleen) suggesting the possibility of viral tropism and possible adaptation to the host. No serological tests were performed. BioMed Central 2020-06-15 /pmc/articles/PMC7296627/ /pubmed/32539799 http://dx.doi.org/10.1186/s13104-020-05137-8 Text en © The Author(s) 2020 Open AccessThis 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Data Note Nikiforuk, A. M. Tierny, K. Cutts, T. A. Kobasa, D. K. Theriault, S. S. Cook, B. W. M. Kyasanur Forest disease virus non-mouse animal models: a pilot study |
title | Kyasanur Forest disease virus non-mouse animal models: a pilot study |
title_full | Kyasanur Forest disease virus non-mouse animal models: a pilot study |
title_fullStr | Kyasanur Forest disease virus non-mouse animal models: a pilot study |
title_full_unstemmed | Kyasanur Forest disease virus non-mouse animal models: a pilot study |
title_short | Kyasanur Forest disease virus non-mouse animal models: a pilot study |
title_sort | kyasanur forest disease virus non-mouse animal models: a pilot study |
topic | Data Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7296627/ https://www.ncbi.nlm.nih.gov/pubmed/32539799 http://dx.doi.org/10.1186/s13104-020-05137-8 |
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