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A novel and sensitive real-time PCR system for universal detection of poxviruses

Success in smallpox eradication was enabled by the absence of non-human reservoir for smallpox virus. However, other poxviruses with a wider host spectrum can infect humans and represent a potential health threat to humans, highlighted by a progressively increasing number of infections by (re)emergi...

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Detalles Bibliográficos
Autores principales: Luciani, Léa, Inchauste, Lucia, Ferraris, Olivier, Charrel, Rémi, Nougairède, Antoine, Piorkowski, Géraldine, Peyrefitte, Christophe, Bertagnoli, Stéphane, de Lamballerie, Xavier, Priet, Stéphane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7815923/
https://www.ncbi.nlm.nih.gov/pubmed/33469067
http://dx.doi.org/10.1038/s41598-021-81376-4
Descripción
Sumario:Success in smallpox eradication was enabled by the absence of non-human reservoir for smallpox virus. However, other poxviruses with a wider host spectrum can infect humans and represent a potential health threat to humans, highlighted by a progressively increasing number of infections by (re)emerging poxviruses, requiring new improved diagnostic and epidemiological tools. We describe here a real-time PCR assay targeting a highly conserved region of the poxvirus genome, thus allowing a pan-Poxvirus detection (Chordopoxvirinae and Entomopoxvirinae). This system is specific (99.8% for vertebrate samples and 99.7% for arthropods samples), sensitive (100% for vertebrate samples and 86.3% for arthropods samples) and presents low limit of detection (< 1000 DNA copies/reaction). In addition, this system could be also valuable for virus discovery and epidemiological projects.