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Development of a colorimetric loop-mediated isothermal amplification assay for rapid and specific detection of Aves polyomavirus 1 from psittacine birds.
Park, Min-Ji; Kim, Hye-Ryung; Chae, Ha-Gyeong; Lim, Da-Rae; Kwon, Oh-Deog; Cho, Kwang-Hyun; Park, Choi-Kyu.
Afiliación
  • Park MJ; College of Veterinary Medicine & Animal Disease Intervention Center, Kyungpook National University, Daegu, 41566, Republic of Korea.
  • Kim HR; College of Veterinary Medicine & Animal Disease Intervention Center, Kyungpook National University, Daegu, 41566, Republic of Korea.
  • Chae HG; College of Veterinary Medicine & Animal Disease Intervention Center, Kyungpook National University, Daegu, 41566, Republic of Korea.
  • Lim DR; College of Veterinary Medicine & Animal Disease Intervention Center, Kyungpook National University, Daegu, 41566, Republic of Korea.
  • Kwon OD; College of Veterinary Medicine & Animal Disease Intervention Center, Kyungpook National University, Daegu, 41566, Republic of Korea.
  • Cho KH; Gyeongbuk Veterinary Service Laboratory, Daegu, 41405, Republic of Korea.
  • Park CK; College of Veterinary Medicine & Animal Disease Intervention Center, Kyungpook National University, Daegu, 41566, Republic of Korea. Electronic address: parkck@knu.ac.kr.
J Virol Methods ; 273: 113687, 2019 11.
Article en En | MEDLINE | ID: mdl-31271791
A colorimetric loop-mediated isothermal amplification (LAMP) assay was developed for the rapid and specific detection of the T gene of Aves polyomavirus 1 (APyV), a causative agent of budgerigar fledgling disease (BFD) in psittacine birds. The amplification can be completed in 40 min at 60 °C, and the results can be visually detected by the naked eye using hydroxyl naphthol blue as a colorimetric indicator. The assay specifically amplified APyV DNA but not other viral and bacterial nucleic acids. The limit of detection of the assay was 5 × 102 DNA copies/reaction, which was comparable to those of previously reported conventional polymerase chain reaction assays. In the clinical evaluation, the LAMP results showed 100% concordance with those of the previously reported PCR assays with regard to specificity, sensitivity, and percentage of overall agreement, with a kappa value of 1.0. These results indicate that the developed LAMP assay will be a valuable tool for the rapid, sensitive and specific detection of APyV from BFD-suspected psittacine bird samples even in resource-limited laboratories.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Loros / Infecciones Tumorales por Virus / Enfermedades de las Aves / Colorimetría / Poliomavirus / Técnicas de Amplificación de Ácido Nucleico / Infecciones por Polyomavirus Tipo de estudio: Diagnostic_studies Límite: Animals Idioma: En Revista: J Virol Methods Año: 2019 Tipo del documento: Article Pais de publicación: Países Bajos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Loros / Infecciones Tumorales por Virus / Enfermedades de las Aves / Colorimetría / Poliomavirus / Técnicas de Amplificación de Ácido Nucleico / Infecciones por Polyomavirus Tipo de estudio: Diagnostic_studies Límite: Animals Idioma: En Revista: J Virol Methods Año: 2019 Tipo del documento: Article Pais de publicación: Países Bajos