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  1. 水産研究・教育機構出版物
  2. 水産研究・教育機構研究報告
  3. 第35号

Development and Evaluation of Real-Time Loop-Mediated Isothermal Amplification Methods for the Rapid Detection of Penaeid Viruses

https://fra.repo.nii.ac.jp/records/2010910
https://fra.repo.nii.ac.jp/records/2010910
589e9fff-6d30-4720-8507-082d343b6985
名前 / ファイル ライセンス アクション
fra_k_35_39.pdf fra_k_35_39.pdf (1.2 MB)
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Item type 紀要論文 / Departmental Bulletin Paper(1)
公開日 2024-10-02
タイトル
タイトル Development and Evaluation of Real-Time Loop-Mediated Isothermal Amplification Methods for the Rapid Detection of Penaeid Viruses
言語 en
言語
言語 eng
キーワード
言語 en
主題Scheme Other
主題 RT-LAMP; WSSV; YHV; IHHNV; TSV; Penaeid shrimp; Japan
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ departmental bulletin paper
アクセス権
アクセス権 open access
アクセス権URI http://purl.org/coar/access_right/c_abf2
著者 米加田, 徹

× 米加田, 徹

WEKO 812
e-Rad 40597944

en Mekata, Toru

ja 米加田, 徹


ja-Kana メカタ, トオル

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SUDHAKARAN, Raja

× SUDHAKARAN, Raja

en SUDHAKARAN, Raja

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ITAMI, Toshiaki

× ITAMI, Toshiaki

en ITAMI, Toshiaki

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抄録
内容記述タイプ Abstract
内容記述 Shrimp viral diseases are a major impediment to commercial shrimp farming. The diseases affecting shrimp culture are white spot syndrome virus (WSSV), yellow head virus (YHV), infectious hypodermal and hematopoietic necrosis virus (IHHNV), and Taura syndrome virus (TSV). Viral diseases are particularly difficult to control after the onset of infection. Therefore, prophylaxes to prevent or reduce the losses through vertical and horizontal transmission are most important. Various diagnostic methods have been developed to detect shrimp viral diseases, including bioassays, histopathology, polymerase chain reaction (PCR), and quantitative real-time PCR. Although the PCR-based methods are sensitive and highly specific, they require expensive equipment, costly reagents, and are time consuming. Therefore, a simple, quick and sensitive detection method is urgently needed to prevent the invasion of shrimp viral diseases into Japan from other countries. The loop-mediated isothermal amplification (LAMP) assay is a novel approach to amplify nucleic acid with high specificity, sensitivity, and rapidity under isothermal conditions, thereby obviating the need for a thermal cycler. Further, during the LAMP reaction, an insoluble byproduct, magnesium pyrophosphate, is produced in proportion to the large amounts of the target DNA amplified. Hence, real-time quantification can be achieved by measuring the turbidity of the magnesium pyrophosphate using an inexpensive photometer. This real-time LAMP method allows quantitative analysis of nucleic acid templates (real-time LAMP). In the present study, a comparatively less expensive quantitative real-time LAMP assay was successfully applied for detection of shrimp viral diseases and proven to have high sensitivity and specificity.
言語 en
書誌情報 ja : 水産総合研究センター研究報告
en : Bulletin of Fisheries Research Agency

巻 35, p. 39-50, ページ数 12, 発行日 2012-01
出版者
出版者 水産総合研究センター
言語 ja
ISSN
収録物識別子タイプ PISSN
収録物識別子 1346-9894
書誌レコードID
収録物識別子タイプ NCID
収録物識別子 AA11589591
情報源
識別子タイプ Local
関連識別子 fra_k_35_39
著者版フラグ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
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