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Detection of Capripoxvirus DNA Using a Field-Ready Nucleic Acid Extraction and Real-Time PCR Platform.
Armson, B; Fowler, V L; Tuppurainen, E S M; Howson, E L A; Madi, M; Sallu, R; Kasanga, C J; Pearson, C; Wood, J; Martin, P; Mioulet, V; King, D P.
Afiliación
  • Armson B; The Pirbright Institute, Surrey, UK.
  • Fowler VL; Institute of Biodiversity, Animal Health and Comparative Medicine, University of Glasgow, Glasgow, UK.
  • Tuppurainen ESM; The Pirbright Institute, Surrey, UK.
  • Howson ELA; The Pirbright Institute, Surrey, UK.
  • Madi M; The Pirbright Institute, Surrey, UK.
  • Sallu R; Institute of Biodiversity, Animal Health and Comparative Medicine, University of Glasgow, Glasgow, UK.
  • Kasanga CJ; The Pirbright Institute, Surrey, UK.
  • Pearson C; Tanzania Veterinary Laboratory Agency (TVLA), Dar-es-Salaam, Tanzania.
  • Wood J; Faculty of Veterinary Medicine, Sokoine University of Agriculture, Morogoro, Tanzania.
  • Martin P; The Pirbright Institute, Surrey, UK.
  • Mioulet V; Enigma Diagnostics, DSTL Porton Down, Salisbury, UK.
  • King DP; Enigma Diagnostics, DSTL Porton Down, Salisbury, UK.
Transbound Emerg Dis ; 64(3): 994-997, 2017 Jun.
Article en En | MEDLINE | ID: mdl-26608662
Capripoxviruses, comprising sheep pox virus, goat pox virus and lumpy skin disease virus cause serious diseases of domesticated ruminants, notifiable to The World Organization for Animal Health. This report describes the evaluation of a mobile diagnostic system (Enigma Field Laboratory) that performs automated sequential steps for nucleic acid extraction and real-time PCR to detect capripoxvirus DNA within laboratory and endemic field settings. To prepare stable reagents that could be deployed into field settings, lyophilized reagents were used that employed an established diagnostic PCR assay. These stabilized reagents demonstrated an analytical sensitivity that was equivalent, or greater than the established laboratory-based PCR test which utilizes wet reagents, and the limit of detection for the complete assay pipeline was approximately one log10 more sensitive than the laboratory-based PCR assay. Concordant results were generated when the mobile PCR system was compared to the laboratory-based PCR using samples collected from Africa, Asia and Europe (n = 10) and experimental studies (n = 9) representing clinical cases of sheep pox, goat pox and lumpy skin disease. Furthermore, this mobile assay reported positive results in situ using specimens that were collected from a dairy cow in Morogoro, Tanzania, which was exhibiting clinical signs of lumpy skin disease. These data support the use of mobile PCR systems for the rapid and sensitive detection of capripoxvirus DNA in endemic field settings.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: ADN Viral / Capripoxvirus / Infecciones por Poxviridae / Reacción en Cadena en Tiempo Real de la Polimerasa Tipo de estudio: Diagnostic_studies Límite: Animals País/Región como asunto: Africa Idioma: En Revista: Transbound Emerg Dis Asunto de la revista: MEDICINA VETERINARIA Año: 2017 Tipo del documento: Article Pais de publicación: Alemania

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: ADN Viral / Capripoxvirus / Infecciones por Poxviridae / Reacción en Cadena en Tiempo Real de la Polimerasa Tipo de estudio: Diagnostic_studies Límite: Animals País/Región como asunto: Africa Idioma: En Revista: Transbound Emerg Dis Asunto de la revista: MEDICINA VETERINARIA Año: 2017 Tipo del documento: Article Pais de publicación: Alemania