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Reverse-transcription recombinase-aided amplification assay for H7 subtype avian influenza virus.
Wang, Suchun; Huang, Baoxu; Ma, Xuejun; Liu, Ping; Wang, Yang; Zhang, Xiaoguang; Zhu, Lin; Fan, Qingying; Sun, Yawei; Wang, Kaicheng.
Afiliación
  • Wang S; China Animal Health and Epidemiology Center, Qingdao, China.
  • Huang B; China Animal Health and Epidemiology Center, Qingdao, China.
  • Ma X; Chinese Center for Disease Control and Prevention, National Institute for Viral Disease Control and Prevention, Beijing, China.
  • Liu P; China Animal Health and Epidemiology Center, Qingdao, China.
  • Wang Y; Key Laboratory of Molecular Pathogen and Immunology of Animal of Luoyang, College of Animal Science and Technology, Henan University of Science and Technology, Luoyang, China.
  • Zhang X; Chinese Center for Disease Control and Prevention, National Institute for Viral Disease Control and Prevention, Beijing, China.
  • Zhu L; China Animal Health and Epidemiology Center, Qingdao, China.
  • Fan Q; Key Laboratory of Molecular Pathogen and Immunology of Animal of Luoyang, College of Animal Science and Technology, Henan University of Science and Technology, Luoyang, China.
  • Sun Y; Key Laboratory of Molecular Pathogen and Immunology of Animal of Luoyang, College of Animal Science and Technology, Henan University of Science and Technology, Luoyang, China.
  • Wang K; China Animal Health and Epidemiology Center, Qingdao, China.
Transbound Emerg Dis ; 67(2): 877-883, 2020 Mar.
Article en En | MEDLINE | ID: mdl-31714018
H7 subtype avian influenza virus infection is an emerging zoonosis in some Asian countries and an important avian disease worldwide. A rapid and simple test is needed to confirm infection in suspected cases during disease outbreaks. In this study, we developed a reverse-transcription recombinase-aided amplification assay for the detection of H7 subtype avian influenza virus. Assays were performed at a single temperature (39°C), and the results were obtained within 20 min. The assay showed no cross-detection with Newcastle disease virus or infectious bronchitis virus, which are the other main respiratory viruses affecting birds. The analytical sensitivity was 102 RNA copies per reaction at a 95% probability level according to probit regression analysis, with 100% specificity. Compared with published reverse-transcription quantitative real-time polymerase chain reaction assays, the κ value of the reverse-transcription recombinase-aided amplification assay in 342 avian clinical samples was 0.988 (p < .001). The sensitivity for avian clinical sample detection was 100% (95%CI, 90.40%-100%), and the specificity was 99.96% (95%CI, 97.83%-99.98%). These results indicated that our reverse-transcription recombinase-aided amplification assay may be a valuable tool for detecting avian influenza H7 subtype virus.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Virus de la Influenza A / Reacción en Cadena de la Polimerasa de Transcriptasa Inversa / Recombinasas / Gripe Humana / Gripe Aviar Tipo de estudio: Diagnostic_studies / Evaluation_studies Límite: Animals / Humans Idioma: En Revista: Transbound Emerg Dis Asunto de la revista: MEDICINA VETERINARIA Año: 2020 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Virus de la Influenza A / Reacción en Cadena de la Polimerasa de Transcriptasa Inversa / Recombinasas / Gripe Humana / Gripe Aviar Tipo de estudio: Diagnostic_studies / Evaluation_studies Límite: Animals / Humans Idioma: En Revista: Transbound Emerg Dis Asunto de la revista: MEDICINA VETERINARIA Año: 2020 Tipo del documento: Article País de afiliación: China