Development and validation of a TaqMan probe-based real-time PCR method for the differentiation of wild type lumpy skin disease virus from vaccine virus strains
Autor: | Serafeim C. Chaintoutis, Andy Haegeman, Achilleas Sachpatzidis, Eleni Chondrokouki, Ilse De Leeuw, Kris De Clercq, Thomas Alexandropoulos, Eirini I. Agianniotaki, Zoe S. Polizopoulou, Konstantia E. Tasioudi, Panagiotis-Dimitrios Katsoulos, Chrysostomos I. Dovas |
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Rok vydání: | 2017 |
Předmět: |
0301 basic medicine
Lumpy Skin Disease Biology Real-Time Polymerase Chain Reaction Vaccines Attenuated Sensitivity and Specificity 03 medical and health sciences Lumpy skin disease Virology medicine TaqMan Animals Attenuated vaccine Wild type Viral Vaccines medicine.disease Lumpy skin disease virus Diva 030104 developmental biology Real-time polymerase chain reaction DNA Viral Cattle Viral disease DNA Probes |
Zdroj: | Journal of Virological Methods. 249:48-57 |
ISSN: | 0166-0934 |
DOI: | 10.1016/j.jviromet.2017.08.011 |
Popis: | Lumpy skin disease (LSD) is a transboundary viral disease of cattle with severe economic impact. Immunization of cattle with homologous live attenuated vaccines poses a number of diagnostic problems, as it has been associated with adverse reactions resembling disease symptoms. The latter hampers clinical diagnosis and poses challenges in virus identification. To this end, a duplex quantitative real-time PCR method targeting the GPCR gene was developed and validated, for the concurrent detection and differentiation of wild type and vaccine Lumpy skin disease virus (LSDV) strains. The method was evaluated in three laboratories. The evaluation included a panel of 38 poxvirus isolates/strains and the analytical characteristics of the method were determined. Amplification efficiencies were 91.3% and 90.7%, for wild type and vaccine LSDV, respectively; the limit of detection was 8 DNA copies for both targets and the inter-assay CV was 0.30% for wild type and 0.73% for vaccine LSDV. The diagnostic performance was assessed using 163 LSDV-positive samples, including field specimens and samples from experimentally vaccinated/infected animals. The method is able to confirm diagnosis in suspect cases, it differentiates infected from vaccinated animals (DIVA) and can be regarded as an important tool for effective LSD surveillance and eradication during vaccination campaigns. |
Databáze: | OpenAIRE |
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