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Multiplex PCR for rapid diagnosis and differentiation of pox and pox-like diseases in dromedary Camels
BACKGROUND: Pox and pox-like diseases of camels are a group of exanthematous skin conditions that have become increasingly important economically. Three distinct viruses may cause them: camelpox virus (CMLV), camel parapox virus (CPPV) and camelus dromedary papilloma virus (CdPV). These diseases are...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4491865/ https://www.ncbi.nlm.nih.gov/pubmed/26148497 http://dx.doi.org/10.1186/s12985-015-0329-x |
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author | Khalafalla, Abdelmalik I Al-Busada, Khalid A El-Sabagh, Ibrahim M |
author_facet | Khalafalla, Abdelmalik I Al-Busada, Khalid A El-Sabagh, Ibrahim M |
author_sort | Khalafalla, Abdelmalik I |
collection | PubMed |
description | BACKGROUND: Pox and pox-like diseases of camels are a group of exanthematous skin conditions that have become increasingly important economically. Three distinct viruses may cause them: camelpox virus (CMLV), camel parapox virus (CPPV) and camelus dromedary papilloma virus (CdPV). These diseases are often difficult to differentiate based on clinical presentation in disease outbreaks. Molecular methods such as PCR targeting species-specific genes have been developed and used to identify these diseases, but not simultaneously in a single tube. Recently, multiplex PCR has gained reputation as a convenient diagnostic method with cost-and timesaving benefits. METHODS AND RESULTS: In the present communication, we describe the development, optimization and validation of a multiplex PCR assay able to detect simultaneously the genome of the three viruses in one single test allowing for rapid and efficient molecular diagnosis. The assay was developed based on the evaluation and combination of published and new primer sets and was validated with viral genomic DNA extracted from known virus strains (n = 14) and DNA extracted from homogenized clinical skin specimens (n = 86). The assay detects correctly the target pathogens by amplification of targeted genes, even in case of co-infection. The method showed high sensitivity, and the specificity was confirmed by PCR-product sequencing. CONCLUSION: This assay provide rapid, sensitive and specific method for identifying three important viruses in specimens collected from dromedary camels with varying clinical presentations. |
format | Online Article Text |
id | pubmed-4491865 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-44918652015-07-07 Multiplex PCR for rapid diagnosis and differentiation of pox and pox-like diseases in dromedary Camels Khalafalla, Abdelmalik I Al-Busada, Khalid A El-Sabagh, Ibrahim M Virol J Research BACKGROUND: Pox and pox-like diseases of camels are a group of exanthematous skin conditions that have become increasingly important economically. Three distinct viruses may cause them: camelpox virus (CMLV), camel parapox virus (CPPV) and camelus dromedary papilloma virus (CdPV). These diseases are often difficult to differentiate based on clinical presentation in disease outbreaks. Molecular methods such as PCR targeting species-specific genes have been developed and used to identify these diseases, but not simultaneously in a single tube. Recently, multiplex PCR has gained reputation as a convenient diagnostic method with cost-and timesaving benefits. METHODS AND RESULTS: In the present communication, we describe the development, optimization and validation of a multiplex PCR assay able to detect simultaneously the genome of the three viruses in one single test allowing for rapid and efficient molecular diagnosis. The assay was developed based on the evaluation and combination of published and new primer sets and was validated with viral genomic DNA extracted from known virus strains (n = 14) and DNA extracted from homogenized clinical skin specimens (n = 86). The assay detects correctly the target pathogens by amplification of targeted genes, even in case of co-infection. The method showed high sensitivity, and the specificity was confirmed by PCR-product sequencing. CONCLUSION: This assay provide rapid, sensitive and specific method for identifying three important viruses in specimens collected from dromedary camels with varying clinical presentations. BioMed Central 2015-07-07 /pmc/articles/PMC4491865/ /pubmed/26148497 http://dx.doi.org/10.1186/s12985-015-0329-x Text en © Khalafalla et al. 2015 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 work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Khalafalla, Abdelmalik I Al-Busada, Khalid A El-Sabagh, Ibrahim M Multiplex PCR for rapid diagnosis and differentiation of pox and pox-like diseases in dromedary Camels |
title | Multiplex PCR for rapid diagnosis and differentiation of pox and pox-like diseases in dromedary Camels |
title_full | Multiplex PCR for rapid diagnosis and differentiation of pox and pox-like diseases in dromedary Camels |
title_fullStr | Multiplex PCR for rapid diagnosis and differentiation of pox and pox-like diseases in dromedary Camels |
title_full_unstemmed | Multiplex PCR for rapid diagnosis and differentiation of pox and pox-like diseases in dromedary Camels |
title_short | Multiplex PCR for rapid diagnosis and differentiation of pox and pox-like diseases in dromedary Camels |
title_sort | multiplex pcr for rapid diagnosis and differentiation of pox and pox-like diseases in dromedary camels |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4491865/ https://www.ncbi.nlm.nih.gov/pubmed/26148497 http://dx.doi.org/10.1186/s12985-015-0329-x |
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