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Simultaneous detection of Zika, Chikungunya and Dengue viruses by a multiplex real-time RT-PCR assay.
Pabbaraju, Kanti; Wong, Sallene; Gill, Kara; Fonseca, Kevin; Tipples, Graham A; Tellier, Raymond.
Afiliación
  • Pabbaraju K; Provincial Laboratory for Public Health, Calgary, Alberta, Canada. Electronic address: kanti.pabbaraju@ahs.ca.
  • Wong S; Provincial Laboratory for Public Health, Calgary, Alberta, Canada. Electronic address: sallene.wong@ahs.ca.
  • Gill K; Provincial Laboratory for Public Health, Calgary, Alberta, Canada. Electronic address: kara.gill2@ahs.ca.
  • Fonseca K; Provincial Laboratory for Public Health, Calgary, Alberta, Canada; Department of Microbiology, Immunology and Infectious Diseases, University of Calgary, Alberta, Canada University of Calgary, Alberta, Canada. Electronic address: kevin.fonseca@ahs.ca.
  • Tipples GA; Provincial Laboratory for Public Health, Calgary, Alberta, Canada; Department of Pathology and Laboratory Medicine, University of Alberta, Edmonton, Alberta, Canada. Electronic address: graham.tipples@ahs.ca.
  • Tellier R; Provincial Laboratory for Public Health, Calgary, Alberta, Canada; Department of Microbiology, Immunology and Infectious Diseases, University of Calgary, Alberta, Canada University of Calgary, Alberta, Canada. Electronic address: raymond.tellier@ahs.ca.
J Clin Virol ; 83: 66-71, 2016 10.
Article en En | MEDLINE | ID: mdl-27614319
BACKGROUND: In the recent past, arboviruses such as Chikungunya (CHIKV) and Zika (ZIKV) have increased their area of endemicity and presented as an emerging global public health threat. OBJECTIVES: To design an assay for the simultaneous detection of ZIKV, CHIKV and Dengue (DENV) 1-4 from patients with symptoms of arboviral infection. This would be advantageous because of the similar clinical presentation typically encountered with these viruses and their co-circulation in endemic areas. STUDY DESIGN: In this study we have developed and validated a triplex real time reverse transcription PCR assay using hydrolysis probes targeting the non-structural 5 (NS5) region of ZIKV, non-structural protein 4 (nsP4) from CHIKV and 3' untranslated region (3'UTR) of DENV 1-4. RESULTS AND CONCLUSIONS: The 95% LOD by the triplex assay was 15 copies/reaction for DENV-1 and less than 10 copies/reaction for all other viruses. The triplex assay was 100% specific and did not amplify any of the other viruses tested. The assay was reproducible and adaptable to testing different specimen types including serum, plasma, urine, placental tissue, brain tissue and amniotic fluid. This assay can be easily implemented for diagnostic testing of patient samples, even in a high throughput laboratory.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Virus Chikungunya / Técnicas de Diagnóstico Molecular / Virus del Dengue / Reacción en Cadena de la Polimerasa Multiplex / Reacción en Cadena en Tiempo Real de la Polimerasa / Virus Zika Tipo de estudio: Diagnostic_studies Idioma: En Revista: J Clin Virol Asunto de la revista: VIROLOGIA Año: 2016 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Virus Chikungunya / Técnicas de Diagnóstico Molecular / Virus del Dengue / Reacción en Cadena de la Polimerasa Multiplex / Reacción en Cadena en Tiempo Real de la Polimerasa / Virus Zika Tipo de estudio: Diagnostic_studies Idioma: En Revista: J Clin Virol Asunto de la revista: VIROLOGIA Año: 2016 Tipo del documento: Article