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Angiostrongylosis in dogs with negative fecal and in‐clinic rapid serological tests: 7 Cases (2013‐2017)
BACKGROUND: Angiostrongylosis is considered as emerging disease in dogs in Belgium. Detection of first‐stage larvae in feces using the Baermann method has an imperfect sensitivity. OBJECTIVES: Investigation of efficacy of noninvasive blood and fecal diagnostic tests in comparison with PCR on broncho...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5980360/ https://www.ncbi.nlm.nih.gov/pubmed/29601653 http://dx.doi.org/10.1111/jvim.15092 |
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author | Canonne, A. Morgane Billen, F. Losson, B. Peters, I. Schnyder, M. Clercx, C. |
author_facet | Canonne, A. Morgane Billen, F. Losson, B. Peters, I. Schnyder, M. Clercx, C. |
author_sort | Canonne, A. Morgane |
collection | PubMed |
description | BACKGROUND: Angiostrongylosis is considered as emerging disease in dogs in Belgium. Detection of first‐stage larvae in feces using the Baermann method has an imperfect sensitivity. OBJECTIVES: Investigation of efficacy of noninvasive blood and fecal diagnostic tests in comparison with PCR on bronchoalveolar lavage (BAL) material in a small series of coughing or dyspnoeic dogs naturally infected with Angiostrongylus vasorum. ANIMALS: Seven dogs with angiostrongylosis. METHODS: Retrospective study. Dogs with cough, exercise intolerance and dyspnea of 2‐ to 8‐week duration. Diagnostic methods used included Baermann analysis, AngioDetect rapid assay, ELISAs for detection of circulating antigen and specific antibodies and qPCR on BAL material. RESULTS: Baermann analysis, AngioDetect rapid assay, antigen ELISA, antibody ELISA, and qPCR on BAL material were positive in 3/7, 2/7, 3/6, 6/6, and 7/7 dogs, respectively. ELISA for antibodies or qPCR on BAL material were essential for definitive diagnosis in 3 dogs. Relative sensitivities of AngioDetect rapid assay, Baermann analysis, and ELISA for antigen detection were lower than 50% compared with ELISA for antibodies or qPCR on BAL material. CONCLUSION AND CLINICAL IMPORTANCE: In this small clinical series, Baermann analysis and AngioDetect rapid assay failed to confirm the diagnosis in some dogs. Therefore, ELISA for antibody detection and qPCR on BAL material should strongly be considered in clinically suspected dogs when antigen detection methods (AngioDetect or ELISA) and Baermann analysis are negative. |
format | Online Article Text |
id | pubmed-5980360 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-59803602018-06-06 Angiostrongylosis in dogs with negative fecal and in‐clinic rapid serological tests: 7 Cases (2013‐2017) Canonne, A. Morgane Billen, F. Losson, B. Peters, I. Schnyder, M. Clercx, C. J Vet Intern Med SMALL ANIMAL BACKGROUND: Angiostrongylosis is considered as emerging disease in dogs in Belgium. Detection of first‐stage larvae in feces using the Baermann method has an imperfect sensitivity. OBJECTIVES: Investigation of efficacy of noninvasive blood and fecal diagnostic tests in comparison with PCR on bronchoalveolar lavage (BAL) material in a small series of coughing or dyspnoeic dogs naturally infected with Angiostrongylus vasorum. ANIMALS: Seven dogs with angiostrongylosis. METHODS: Retrospective study. Dogs with cough, exercise intolerance and dyspnea of 2‐ to 8‐week duration. Diagnostic methods used included Baermann analysis, AngioDetect rapid assay, ELISAs for detection of circulating antigen and specific antibodies and qPCR on BAL material. RESULTS: Baermann analysis, AngioDetect rapid assay, antigen ELISA, antibody ELISA, and qPCR on BAL material were positive in 3/7, 2/7, 3/6, 6/6, and 7/7 dogs, respectively. ELISA for antibodies or qPCR on BAL material were essential for definitive diagnosis in 3 dogs. Relative sensitivities of AngioDetect rapid assay, Baermann analysis, and ELISA for antigen detection were lower than 50% compared with ELISA for antibodies or qPCR on BAL material. CONCLUSION AND CLINICAL IMPORTANCE: In this small clinical series, Baermann analysis and AngioDetect rapid assay failed to confirm the diagnosis in some dogs. Therefore, ELISA for antibody detection and qPCR on BAL material should strongly be considered in clinically suspected dogs when antigen detection methods (AngioDetect or ELISA) and Baermann analysis are negative. John Wiley and Sons Inc. 2018-03-30 2018 /pmc/articles/PMC5980360/ /pubmed/29601653 http://dx.doi.org/10.1111/jvim.15092 Text en Copyright © 2018 The Authors. Journal of Veterinary Internal Medicine published by Wiley Periodicals, Inc. on behalf of the American College of Veterinary Internal Medicine. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | SMALL ANIMAL Canonne, A. Morgane Billen, F. Losson, B. Peters, I. Schnyder, M. Clercx, C. Angiostrongylosis in dogs with negative fecal and in‐clinic rapid serological tests: 7 Cases (2013‐2017) |
title | Angiostrongylosis in dogs with negative fecal and in‐clinic rapid serological tests: 7 Cases (2013‐2017) |
title_full | Angiostrongylosis in dogs with negative fecal and in‐clinic rapid serological tests: 7 Cases (2013‐2017) |
title_fullStr | Angiostrongylosis in dogs with negative fecal and in‐clinic rapid serological tests: 7 Cases (2013‐2017) |
title_full_unstemmed | Angiostrongylosis in dogs with negative fecal and in‐clinic rapid serological tests: 7 Cases (2013‐2017) |
title_short | Angiostrongylosis in dogs with negative fecal and in‐clinic rapid serological tests: 7 Cases (2013‐2017) |
title_sort | angiostrongylosis in dogs with negative fecal and in‐clinic rapid serological tests: 7 cases (2013‐2017) |
topic | SMALL ANIMAL |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5980360/ https://www.ncbi.nlm.nih.gov/pubmed/29601653 http://dx.doi.org/10.1111/jvim.15092 |
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