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Diagnostic Uncertainty and the Epidemiology of Feline Foamy Virus in Pumas (Puma concolor)

Feline foamy virus (FFV) is a contact-dependent retrovirus forming chronic, largely apathogenic, infections in domestic and wild felid populations worldwide. Given there is no current ‘gold standard’ diagnostic test for FFV, efforts to elucidate the ecology and epidemiology of the virus may be compl...

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Autores principales: Dannemiller, Nicholas G., Kechejian, Sarah, Kraberger, Simona, Logan, Kenneth, Alldredge, Mathew, Crooks, Kevin R., VandeWoude, Sue, Carver, Scott
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6994588/
https://www.ncbi.nlm.nih.gov/pubmed/32005906
http://dx.doi.org/10.1038/s41598-020-58350-7
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author Dannemiller, Nicholas G.
Kechejian, Sarah
Kraberger, Simona
Logan, Kenneth
Alldredge, Mathew
Crooks, Kevin R.
VandeWoude, Sue
Carver, Scott
author_facet Dannemiller, Nicholas G.
Kechejian, Sarah
Kraberger, Simona
Logan, Kenneth
Alldredge, Mathew
Crooks, Kevin R.
VandeWoude, Sue
Carver, Scott
author_sort Dannemiller, Nicholas G.
collection PubMed
description Feline foamy virus (FFV) is a contact-dependent retrovirus forming chronic, largely apathogenic, infections in domestic and wild felid populations worldwide. Given there is no current ‘gold standard’ diagnostic test for FFV, efforts to elucidate the ecology and epidemiology of the virus may be complicated by unknown sensitivity and specificity of diagnostic tests. Using Bayesian Latent Class Analysis, we estimated the sensitivity and specificity of the only two FFV diagnostic tests available—ELISA and qPCR—as well as the prevalence of FFV in a large cohort of pumas from Colorado. We evaluated the diagnostic agreement of ELISA and qPCR, and whether differences in their diagnostic accuracy impacted risk factor analyses for FFV infection. Our results suggest ELISA and qPCR did not have strong diagnostic agreement, despite FFV causing a persistent infection. While both tests had similar sensitivity, ELISA had higher specificity. ELISA, but not qPCR, identified age to be a significant risk factor, whereas neither qPCR nor ELISA identified sex to be a risk factor. This suggests FFV transmission in pumas may primarily be via non-antagonistic, social interactions between adult conspecifics. Our study highlights that combined use of qPCR and ELISA for FFV may enhance estimates of the true prevalence of FFV and epidemiological inferences.
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spelling pubmed-69945882020-02-06 Diagnostic Uncertainty and the Epidemiology of Feline Foamy Virus in Pumas (Puma concolor) Dannemiller, Nicholas G. Kechejian, Sarah Kraberger, Simona Logan, Kenneth Alldredge, Mathew Crooks, Kevin R. VandeWoude, Sue Carver, Scott Sci Rep Article Feline foamy virus (FFV) is a contact-dependent retrovirus forming chronic, largely apathogenic, infections in domestic and wild felid populations worldwide. Given there is no current ‘gold standard’ diagnostic test for FFV, efforts to elucidate the ecology and epidemiology of the virus may be complicated by unknown sensitivity and specificity of diagnostic tests. Using Bayesian Latent Class Analysis, we estimated the sensitivity and specificity of the only two FFV diagnostic tests available—ELISA and qPCR—as well as the prevalence of FFV in a large cohort of pumas from Colorado. We evaluated the diagnostic agreement of ELISA and qPCR, and whether differences in their diagnostic accuracy impacted risk factor analyses for FFV infection. Our results suggest ELISA and qPCR did not have strong diagnostic agreement, despite FFV causing a persistent infection. While both tests had similar sensitivity, ELISA had higher specificity. ELISA, but not qPCR, identified age to be a significant risk factor, whereas neither qPCR nor ELISA identified sex to be a risk factor. This suggests FFV transmission in pumas may primarily be via non-antagonistic, social interactions between adult conspecifics. Our study highlights that combined use of qPCR and ELISA for FFV may enhance estimates of the true prevalence of FFV and epidemiological inferences. Nature Publishing Group UK 2020-01-31 /pmc/articles/PMC6994588/ /pubmed/32005906 http://dx.doi.org/10.1038/s41598-020-58350-7 Text en © The Author(s) 2020 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Dannemiller, Nicholas G.
Kechejian, Sarah
Kraberger, Simona
Logan, Kenneth
Alldredge, Mathew
Crooks, Kevin R.
VandeWoude, Sue
Carver, Scott
Diagnostic Uncertainty and the Epidemiology of Feline Foamy Virus in Pumas (Puma concolor)
title Diagnostic Uncertainty and the Epidemiology of Feline Foamy Virus in Pumas (Puma concolor)
title_full Diagnostic Uncertainty and the Epidemiology of Feline Foamy Virus in Pumas (Puma concolor)
title_fullStr Diagnostic Uncertainty and the Epidemiology of Feline Foamy Virus in Pumas (Puma concolor)
title_full_unstemmed Diagnostic Uncertainty and the Epidemiology of Feline Foamy Virus in Pumas (Puma concolor)
title_short Diagnostic Uncertainty and the Epidemiology of Feline Foamy Virus in Pumas (Puma concolor)
title_sort diagnostic uncertainty and the epidemiology of feline foamy virus in pumas (puma concolor)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6994588/
https://www.ncbi.nlm.nih.gov/pubmed/32005906
http://dx.doi.org/10.1038/s41598-020-58350-7
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