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Detection of selected viral pathogens in dogs with canine infectious respiratory disease in Austria

OBJECTIVES: To assess the prevalence of canine parainfluenza virus, canine adenovirus type 2, canine distemper virus, canine respiratory coronavirus and influenza virus A infections in: (1) privately‐owned or, (2) kennelled dogs showing signs consistent with canine infectious respiratory disease and...

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Autores principales: Hiebl, A., Auer, A., Bagrinovschi, G., Stejskal, M., Hirt, R., Rümenapf, H. T., Tichy, A., Künzel, F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6852529/
https://www.ncbi.nlm.nih.gov/pubmed/31301071
http://dx.doi.org/10.1111/jsap.13051
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author Hiebl, A.
Auer, A.
Bagrinovschi, G.
Stejskal, M.
Hirt, R.
Rümenapf, H. T.
Tichy, A.
Künzel, F.
author_facet Hiebl, A.
Auer, A.
Bagrinovschi, G.
Stejskal, M.
Hirt, R.
Rümenapf, H. T.
Tichy, A.
Künzel, F.
author_sort Hiebl, A.
collection PubMed
description OBJECTIVES: To assess the prevalence of canine parainfluenza virus, canine adenovirus type 2, canine distemper virus, canine respiratory coronavirus and influenza virus A infections in: (1) privately‐owned or, (2) kennelled dogs showing signs consistent with canine infectious respiratory disease and, (3) clinically healthy dogs in Vienna, Austria. MATERIALS AND METHODS: Prospectively, nasal and tonsillar swabs from 214 dogs affected with infectious respiratory disease, and 50 healthy control dogs were tested for nucleic acids specific to the various viral infections. Concurrent bronchoalveolar lavage fluid from 31 dogs with chronic respiratory disease was investigated for the same viral pathogens. Additionally, anti‐canine respiratory coronavirus antibody concentrations were measured in paired blood samples from 30 acutely diseased dogs. RESULTS: Canine respiratory coronavirus (7.5%) and canine parainfluenza virus (6.5%) were the most commonly detected viruses in samples from the upper airways of dogs with respiratory infections. Serological results showed a significant seroconversion in response to coronavirus in 50% of the examined cases. None of the samples was positive for influenza virus A‐specific nucleic acid. Canine coronavirus‐specific nucleic acid was detected in 4.0% of healthy dogs. CLINICAL SIGNIFICANCE: Canine coronavirus should be considered as a clinically relevant cause of infectious respiratory disease in crowded dog populations. For sample collection, the nasal mucosa can be recommended as the favoured site. Analysis of paired serum samples aids verification of canine coronavirus infection in respiratory disease.
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spelling pubmed-68525292019-11-20 Detection of selected viral pathogens in dogs with canine infectious respiratory disease in Austria Hiebl, A. Auer, A. Bagrinovschi, G. Stejskal, M. Hirt, R. Rümenapf, H. T. Tichy, A. Künzel, F. J Small Anim Pract Papers OBJECTIVES: To assess the prevalence of canine parainfluenza virus, canine adenovirus type 2, canine distemper virus, canine respiratory coronavirus and influenza virus A infections in: (1) privately‐owned or, (2) kennelled dogs showing signs consistent with canine infectious respiratory disease and, (3) clinically healthy dogs in Vienna, Austria. MATERIALS AND METHODS: Prospectively, nasal and tonsillar swabs from 214 dogs affected with infectious respiratory disease, and 50 healthy control dogs were tested for nucleic acids specific to the various viral infections. Concurrent bronchoalveolar lavage fluid from 31 dogs with chronic respiratory disease was investigated for the same viral pathogens. Additionally, anti‐canine respiratory coronavirus antibody concentrations were measured in paired blood samples from 30 acutely diseased dogs. RESULTS: Canine respiratory coronavirus (7.5%) and canine parainfluenza virus (6.5%) were the most commonly detected viruses in samples from the upper airways of dogs with respiratory infections. Serological results showed a significant seroconversion in response to coronavirus in 50% of the examined cases. None of the samples was positive for influenza virus A‐specific nucleic acid. Canine coronavirus‐specific nucleic acid was detected in 4.0% of healthy dogs. CLINICAL SIGNIFICANCE: Canine coronavirus should be considered as a clinically relevant cause of infectious respiratory disease in crowded dog populations. For sample collection, the nasal mucosa can be recommended as the favoured site. Analysis of paired serum samples aids verification of canine coronavirus infection in respiratory disease. Blackwell Publishing Ltd 2019-07-12 2019-10 /pmc/articles/PMC6852529/ /pubmed/31301071 http://dx.doi.org/10.1111/jsap.13051 Text en © 2019 The Authors Journal of Small Animal Practice published by John Wiley & Sons Ltd on behalf of British Small Animal Veterinary Association This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Papers
Hiebl, A.
Auer, A.
Bagrinovschi, G.
Stejskal, M.
Hirt, R.
Rümenapf, H. T.
Tichy, A.
Künzel, F.
Detection of selected viral pathogens in dogs with canine infectious respiratory disease in Austria
title Detection of selected viral pathogens in dogs with canine infectious respiratory disease in Austria
title_full Detection of selected viral pathogens in dogs with canine infectious respiratory disease in Austria
title_fullStr Detection of selected viral pathogens in dogs with canine infectious respiratory disease in Austria
title_full_unstemmed Detection of selected viral pathogens in dogs with canine infectious respiratory disease in Austria
title_short Detection of selected viral pathogens in dogs with canine infectious respiratory disease in Austria
title_sort detection of selected viral pathogens in dogs with canine infectious respiratory disease in austria
topic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6852529/
https://www.ncbi.nlm.nih.gov/pubmed/31301071
http://dx.doi.org/10.1111/jsap.13051
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