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Detection of Clinical and Subclinical Lumpy Skin Disease Using Ear Notch Testing and Skin Biopsies

Lumpy skin disease (LSD) diagnosis is primarily based on clinical surveillance complemented by PCR of lesion crusts or nodule biopsies. Since LSD can be subclinical, the sensitivity of clinical surveillance could be lower than expected. Furthermore, real-time PCR for the detection of LSD viral DNA i...

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Autores principales: Aerts, Laetitia, Haegeman, Andy, De Leeuw, Ilse, Philips, Wannes, Van Campe, Willem, Behaeghel, Isabelle, Mostin, Laurent, De Clercq, Kris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8541182/
https://www.ncbi.nlm.nih.gov/pubmed/34683492
http://dx.doi.org/10.3390/microorganisms9102171
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author Aerts, Laetitia
Haegeman, Andy
De Leeuw, Ilse
Philips, Wannes
Van Campe, Willem
Behaeghel, Isabelle
Mostin, Laurent
De Clercq, Kris
author_facet Aerts, Laetitia
Haegeman, Andy
De Leeuw, Ilse
Philips, Wannes
Van Campe, Willem
Behaeghel, Isabelle
Mostin, Laurent
De Clercq, Kris
author_sort Aerts, Laetitia
collection PubMed
description Lumpy skin disease (LSD) diagnosis is primarily based on clinical surveillance complemented by PCR of lesion crusts or nodule biopsies. Since LSD can be subclinical, the sensitivity of clinical surveillance could be lower than expected. Furthermore, real-time PCR for the detection of LSD viral DNA in blood samples from subclinical animals is only intermittently positive. Therefore, this study aimed to investigate an acceptable, easily applicable and more sensitive testing method for the detection of clinical and subclinical LSD. An animal experiment was conducted to investigate ear notches and biopsies from unaffected skin taken from the neck and dorsal back as alternatives to blood samples. It was concluded that for early LSD confirmation, normal skin biopsies and ear notches are less fit for purpose, as LSDV DNA is only detectable in these samples several days after it is detectable in blood samples. On the other hand, blood samples are less advisable for the detection of subclinical animals, while ear notches and biopsies were positive for LSD viral DNA in all subclinically infected animals by 16 days post infection. In conclusion, ear notches could be used for surveillance to detect subclinical animals after removing the clinical animals from a herd, to regain trade by substantiating the freedom of disease or to support research on LSDV transmission from subclinical animals.
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spelling pubmed-85411822021-10-24 Detection of Clinical and Subclinical Lumpy Skin Disease Using Ear Notch Testing and Skin Biopsies Aerts, Laetitia Haegeman, Andy De Leeuw, Ilse Philips, Wannes Van Campe, Willem Behaeghel, Isabelle Mostin, Laurent De Clercq, Kris Microorganisms Article Lumpy skin disease (LSD) diagnosis is primarily based on clinical surveillance complemented by PCR of lesion crusts or nodule biopsies. Since LSD can be subclinical, the sensitivity of clinical surveillance could be lower than expected. Furthermore, real-time PCR for the detection of LSD viral DNA in blood samples from subclinical animals is only intermittently positive. Therefore, this study aimed to investigate an acceptable, easily applicable and more sensitive testing method for the detection of clinical and subclinical LSD. An animal experiment was conducted to investigate ear notches and biopsies from unaffected skin taken from the neck and dorsal back as alternatives to blood samples. It was concluded that for early LSD confirmation, normal skin biopsies and ear notches are less fit for purpose, as LSDV DNA is only detectable in these samples several days after it is detectable in blood samples. On the other hand, blood samples are less advisable for the detection of subclinical animals, while ear notches and biopsies were positive for LSD viral DNA in all subclinically infected animals by 16 days post infection. In conclusion, ear notches could be used for surveillance to detect subclinical animals after removing the clinical animals from a herd, to regain trade by substantiating the freedom of disease or to support research on LSDV transmission from subclinical animals. MDPI 2021-10-19 /pmc/articles/PMC8541182/ /pubmed/34683492 http://dx.doi.org/10.3390/microorganisms9102171 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Aerts, Laetitia
Haegeman, Andy
De Leeuw, Ilse
Philips, Wannes
Van Campe, Willem
Behaeghel, Isabelle
Mostin, Laurent
De Clercq, Kris
Detection of Clinical and Subclinical Lumpy Skin Disease Using Ear Notch Testing and Skin Biopsies
title Detection of Clinical and Subclinical Lumpy Skin Disease Using Ear Notch Testing and Skin Biopsies
title_full Detection of Clinical and Subclinical Lumpy Skin Disease Using Ear Notch Testing and Skin Biopsies
title_fullStr Detection of Clinical and Subclinical Lumpy Skin Disease Using Ear Notch Testing and Skin Biopsies
title_full_unstemmed Detection of Clinical and Subclinical Lumpy Skin Disease Using Ear Notch Testing and Skin Biopsies
title_short Detection of Clinical and Subclinical Lumpy Skin Disease Using Ear Notch Testing and Skin Biopsies
title_sort detection of clinical and subclinical lumpy skin disease using ear notch testing and skin biopsies
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8541182/
https://www.ncbi.nlm.nih.gov/pubmed/34683492
http://dx.doi.org/10.3390/microorganisms9102171
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