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Antibody response in snakes with boid inclusion body disease
Boid Inclusion Body Disease (BIBD) is a potentially fatal disease reported in captive boid snakes worldwide that is caused by reptarenavirus infection. Although the detection of intracytoplasmic inclusion bodies (IB) in blood cells serves as the gold standard for the ante mortem diagnosis of BIBD, t...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6733472/ https://www.ncbi.nlm.nih.gov/pubmed/31498825 http://dx.doi.org/10.1371/journal.pone.0221863 |
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author | Windbichler, Katharina Michalopoulou, Eleni Palamides, Pia Pesch, Theresa Jelinek, Christine Vapalahti, Olli Kipar, Anja Hetzel, Udo Hepojoki, Jussi |
author_facet | Windbichler, Katharina Michalopoulou, Eleni Palamides, Pia Pesch, Theresa Jelinek, Christine Vapalahti, Olli Kipar, Anja Hetzel, Udo Hepojoki, Jussi |
author_sort | Windbichler, Katharina |
collection | PubMed |
description | Boid Inclusion Body Disease (BIBD) is a potentially fatal disease reported in captive boid snakes worldwide that is caused by reptarenavirus infection. Although the detection of intracytoplasmic inclusion bodies (IB) in blood cells serves as the gold standard for the ante mortem diagnosis of BIBD, the mechanisms underlying IB formation and the pathogenesis of BIBD are unknown. Knowledge on the reptile immune system is sparse compared to the mammalian counterpart, and in particular the response towards reptarenavirus infection is practically unknown. Herein, we investigated a breeding collection of 70 Boa constrictor snakes for BIBD, reptarenavirus viraemia, anti-reptarenavirus IgM and IgY antibodies, and population parameters. Using NGS and RT-PCR on pooled blood samples of snakes with and without BIBD, we could identify three different reptarenavirus S segments in the collection. The examination of individual samples by RT-PCR indicated that the presence of University of Giessen virus (UGV)-like S segment strongly correlates with IB formation. We could also demonstrate a negative correlation between BIBD and the presence of anti-UGV NP IgY antibodies. Further evidence of an association between antibody response and BIBD is the finding that the level of anti-reptarenavirus antibodies measured by ELISA was lower in snakes with BIBD. Furthermore, female snakes had a significantly lower body weight when they had BIBD. Taken together our findings suggest that the detection of the UGV-/S6-like S segment and the presence of anti-reptarenavirus IgY antibodies might serve as a prognostic tool for predicting the development of BIBD. |
format | Online Article Text |
id | pubmed-6733472 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-67334722019-09-20 Antibody response in snakes with boid inclusion body disease Windbichler, Katharina Michalopoulou, Eleni Palamides, Pia Pesch, Theresa Jelinek, Christine Vapalahti, Olli Kipar, Anja Hetzel, Udo Hepojoki, Jussi PLoS One Research Article Boid Inclusion Body Disease (BIBD) is a potentially fatal disease reported in captive boid snakes worldwide that is caused by reptarenavirus infection. Although the detection of intracytoplasmic inclusion bodies (IB) in blood cells serves as the gold standard for the ante mortem diagnosis of BIBD, the mechanisms underlying IB formation and the pathogenesis of BIBD are unknown. Knowledge on the reptile immune system is sparse compared to the mammalian counterpart, and in particular the response towards reptarenavirus infection is practically unknown. Herein, we investigated a breeding collection of 70 Boa constrictor snakes for BIBD, reptarenavirus viraemia, anti-reptarenavirus IgM and IgY antibodies, and population parameters. Using NGS and RT-PCR on pooled blood samples of snakes with and without BIBD, we could identify three different reptarenavirus S segments in the collection. The examination of individual samples by RT-PCR indicated that the presence of University of Giessen virus (UGV)-like S segment strongly correlates with IB formation. We could also demonstrate a negative correlation between BIBD and the presence of anti-UGV NP IgY antibodies. Further evidence of an association between antibody response and BIBD is the finding that the level of anti-reptarenavirus antibodies measured by ELISA was lower in snakes with BIBD. Furthermore, female snakes had a significantly lower body weight when they had BIBD. Taken together our findings suggest that the detection of the UGV-/S6-like S segment and the presence of anti-reptarenavirus IgY antibodies might serve as a prognostic tool for predicting the development of BIBD. Public Library of Science 2019-09-09 /pmc/articles/PMC6733472/ /pubmed/31498825 http://dx.doi.org/10.1371/journal.pone.0221863 Text en © 2019 Windbichler et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Windbichler, Katharina Michalopoulou, Eleni Palamides, Pia Pesch, Theresa Jelinek, Christine Vapalahti, Olli Kipar, Anja Hetzel, Udo Hepojoki, Jussi Antibody response in snakes with boid inclusion body disease |
title | Antibody response in snakes with boid inclusion body disease |
title_full | Antibody response in snakes with boid inclusion body disease |
title_fullStr | Antibody response in snakes with boid inclusion body disease |
title_full_unstemmed | Antibody response in snakes with boid inclusion body disease |
title_short | Antibody response in snakes with boid inclusion body disease |
title_sort | antibody response in snakes with boid inclusion body disease |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6733472/ https://www.ncbi.nlm.nih.gov/pubmed/31498825 http://dx.doi.org/10.1371/journal.pone.0221863 |
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