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Development of a Usutu virus specific real-time reverse transcription PCR assay based on sequenced strains from Africa and Europe.
Nikolay, B; Weidmann, M; Dupressoir, A; Faye, O; Boye, C S; Diallo, M; Sall, A A.
Affiliation
  • Nikolay B; Unité des arbovirus et virus de fièvres hémorragiques, Institut Pasteur de Dakar, 34 Avenue Pasteur, Dakar, Senegal; Université Cheikh Anta Diop Dakar, 24 Avenue Cheikh Anta Diop, Dakar, Senegal; University Vienna, Dr. Bohr-Gasse 9/3, A-1030 Vienna, Austria. Electronic address: birgitnikolay@gmail.c
  • Weidmann M; Department of Virology, University Medical Center Goettingen, Kreuzbergring 57, D-37075 Goettingen, Germany. Electronic address: mweidma@gwdg.de.
  • Dupressoir A; CNRS UMR 8122, Institut Gustave Roussy, Villejuif 94805, France. Electronic address: dupresso@igr.fr.
  • Faye O; Unité des arbovirus et virus de fièvres hémorragiques, Institut Pasteur de Dakar, 34 Avenue Pasteur, Dakar, Senegal. Electronic address: ofaye@pasteur.sn.
  • Boye CS; University Vienna, Dr. Bohr-Gasse 9/3, A-1030 Vienna, Austria. Electronic address: cheikh.boye@ucad.edu.sn.
  • Diallo M; Unité d'entomologie médicale, Institut Pasteur de Dakar, Senegal.
  • Sall AA; Unité des arbovirus et virus de fièvres hémorragiques, Institut Pasteur de Dakar, 34 Avenue Pasteur, Dakar, Senegal. Electronic address: asall@pasteur.sn.
J Virol Methods ; 197: 51-4, 2014 Mar.
Article in En | MEDLINE | ID: mdl-24036076
ABSTRACT
Usutu virus (USUV) has been isolated in several African and European countries mainly from mosquitoes and birds. However, previous benign and two recent severe cases of human infections point out the need of a tool for the identification of USUV in human samples. A published real-time reverse transcription (RT) PCR assay for the detection of USUV in human blood or cerebrospinal fluid does not take into account the genetic variability of USUV in different geographic regions. Therefore, this article presents a quantitative real-time RT-PCR assay based on sequences from Europe and Africa. Primers and probe were designed in conserved regions among USUV strains that differed from closely related flaviviruses. The specificity of the assay was investigated by testing 16 other flaviviruses circulating in Africa. The sensitivity was determined by testing serial dilutions of virus and RNA standard. Intra- and inter-assay coefficients of variation were evaluated by 10 reactions in a same and in different assays, respectively. The assay provides high analytical specificity for USUV and detection limits of 1.2pfu/reaction for virus dilutions in L-15 medium or human serum and 60 copies/reaction for the RNA standard. The assay needs to be evaluated in a clinical context and integrated in standard diagnosis of flaviviral diseases.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Flavivirus Infections / Encephalitis Viruses, Japanese / Reverse Transcriptase Polymerase Chain Reaction / Encephalitis, Arbovirus / Real-Time Polymerase Chain Reaction Type of study: Diagnostic_studies / Prognostic_studies Limits: Humans Country/Region as subject: Africa / Europa Language: En Journal: J Virol Methods Year: 2014 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Flavivirus Infections / Encephalitis Viruses, Japanese / Reverse Transcriptase Polymerase Chain Reaction / Encephalitis, Arbovirus / Real-Time Polymerase Chain Reaction Type of study: Diagnostic_studies / Prognostic_studies Limits: Humans Country/Region as subject: Africa / Europa Language: En Journal: J Virol Methods Year: 2014 Document type: Article