臨床微生物学のアーカイブ

  • ISSN: 1989-8436
  • ジャーナル h-index: 22
  • 雑誌引用スコア: 7.55
  • ジャーナルのインパクトファクター: 6.38
インデックス付き
  • Jゲートを開く
  • Genamics JournalSeek
  • グローバル インパクト ファクター (GIF)
  • オープンアーカイブイニシアチブ
  • 中国国家知識基盤 (CNKI)
  • 研究ジャーナル索引作成ディレクトリ (DRJI)
  • OCLC-WorldCat
  • プロクエスト召喚
  • パブロン
  • ミアル
  • 大学補助金委員会
  • ジュネーブ医学教育研究財団
  • Google スカラー
  • シマゴジャーナルランキング
  • 秘密検索エンジン研究所
  • リサーチゲート
このページをシェアする

抽象的な

Development of a Loop-mediated Isothermal Amplification Method for Rapid Detection of Beak and Feather Disease Virus in Parrots

Yi Hsuan Kuo, Shinn Shyong Tsai, Hung Jen Liu and Kuo Pin Chuang

Background: There are no effective antiviral treatments for Beak and Feather Disease virus (BFDV); thus, rapid diagnosis is critical for effective control of the disease. Recent development of a novel Loop-Mediated Isothermal Amplification (LAMP) technique that amplifies nucleic acids rapidly with high specificity and sensitivity under isothermal conditions has overcome some of the deficiencies of nucleic acid-based diagnostic tests and has made on-site diagnosis possible.

Methods and finding: We established a LAMP method for rapid detection of BFDV using 2 pairs of primers that were designed from BFDV and compared its sensitivity and specificity with PCR. Amplification by LAMP was optimal at 63°C for 60 min. The detection limit was nearly 3.5 fg of BFDV DNA— as sensitive as PCR. There was no cross-reaction with porcine circovirus type 2 (PCV2), pigeon circovirus (PiCV) or avian polyomavirus under the same conditions. The assay also successfully detected BFDV DNA in the tissues of infected parrots.

Conclusion: This is the first report indicating that LAMP is a valuable, rapid method of detecting BFDV with high sensitivity and specificity.