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Development and evaluation of tailored specific real-time RT-PCR assays for detection of foot-and-mouth disease virus serotypes circulating in East Africa.
Bachanek-Bankowska, Katarzyna; Mero, Herieth R; Wadsworth, Jemma; Mioulet, Valerie; Sallu, Raphael; Belsham, Graham J; Kasanga, Christopher J; Knowles, Nick J; King, Donald P.
Afiliación
  • Bachanek-Bankowska K; The Pirbright Institute, Ash Road, Pirbright, Woking, Surrey GU24 0NF, UK. Electronic address: kasia.bankowska@pirbright.ac.uk.
  • Mero HR; Department of Microbiology and Parasitology & Southern African Centre for Infectious diseases Surveillance, Sokoine University of Agriculture, Morogoro, Tanzania.
  • Wadsworth J; The Pirbright Institute, Ash Road, Pirbright, Woking, Surrey GU24 0NF, UK.
  • Mioulet V; The Pirbright Institute, Ash Road, Pirbright, Woking, Surrey GU24 0NF, UK.
  • Sallu R; Tanzania Veterinary Laboratory Agency, P. O. Box 9252, Dar es Salaam, Tanzania.
  • Belsham GJ; National Veterinary Institute, Technical University of Denmark, Lindholm, Kalvehave DK-4771, Denmark.
  • Kasanga CJ; Department of Microbiology and Parasitology & Southern African Centre for Infectious diseases Surveillance, Sokoine University of Agriculture, Morogoro, Tanzania.
  • Knowles NJ; The Pirbright Institute, Ash Road, Pirbright, Woking, Surrey GU24 0NF, UK.
  • King DP; The Pirbright Institute, Ash Road, Pirbright, Woking, Surrey GU24 0NF, UK.
J Virol Methods ; 237: 114-120, 2016 11.
Article en En | MEDLINE | ID: mdl-27575682
Rapid, reliable and accurate diagnostic methods provide essential support to programmes that monitor and control foot-and-mouth disease (FMD). While pan-specific molecular tests for FMD virus (FMDV) detection are well established and widely used in endemic and FMD-free countries, current serotyping methods mainly rely either on antigen detection ELISAs or nucleotide sequencing approaches. This report describes the development of a panel of serotype-specific real-time RT-PCR assays (rRT-PCR) tailored to detect FMDV lineages currently circulating in East Africa. These assays target sequences within the VP1-coding region that share high intra-lineage identity, but do not cross-react with FMD viruses from other serotypes that circulate in the region. These serotype-specific assays operate with the same thermal profile as the pan-diagnostic tests making it possible to run them in parallel to produce CT values comparable to the pan-diagnostic test detecting the 3D-coding region. These assays were evaluated alongside the established pan-specific molecular test using field samples and virus isolates collected from Tanzania, Kenya and Ethiopia that had been previously characterised by nucleotide sequencing. Samples (n=71) representing serotype A (topotype AFRICA, lineage G-I), serotype O (topotypes EA-2 and EA-4), serotype SAT 1 (topotype I (NWZ)) and serotype SAT2 (topotype IV) were correctly identified with these rRT-PCR assays. Furthermore, FMDV RNA from samples that did not contain infectious virus could still be serotyped using these assays. These serotype-specific real-time RT-PCR assays can detect and characterise FMDVs currently circulating in East Africa and hence improve disease control in this region.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Virus de la Fiebre Aftosa / Técnicas de Diagnóstico Molecular / Reacción en Cadena en Tiempo Real de la Polimerasa / Fiebre Aftosa Tipo de estudio: Diagnostic_studies / Evaluation_studies / Prognostic_studies Límite: Animals País/Región como asunto: Africa Idioma: En Revista: J Virol Methods Año: 2016 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Virus de la Fiebre Aftosa / Técnicas de Diagnóstico Molecular / Reacción en Cadena en Tiempo Real de la Polimerasa / Fiebre Aftosa Tipo de estudio: Diagnostic_studies / Evaluation_studies / Prognostic_studies Límite: Animals País/Región como asunto: Africa Idioma: En Revista: J Virol Methods Año: 2016 Tipo del documento: Article