Teeranart PuthawiboolSaengchan SenapinTimothy W. FlegelW. Kiatpathomchai WansikaMahidol UniversityThailand National Center for Genetic Engineering and Biotechnology2018-09-242018-09-242010-10-01Molecular and Cellular Probes. Vol.24, No.5 (2010), 244-249089085082-s2.0-77956064483https://repository.li.mahidol.ac.th/handle/123456789/28631Loop-mediated isothermal amplification (LAMP) allows rapid amplification of nucleic acids under isothermal conditions. It can be combined with a chromatographic lateral flow dipstick (LFD) for much more efficient, field-friendly detection of MrNV. In this work, RT-LAMP was performed at 65 °C for 40 min, followed by 5 min for hybridization with an FITC-labeled DNA probe and 5 min for LFD resulted in visualization of DNA amplicons trapped at the LFD test line. Thus, total assay time, including 10 min for rapid RNA extraction was approximately 60 min. In addition to advantages of short assay time, confirmation of amplicon identity by hybridization and elimination of electrophoresis with carcinogenic ethidium bromide, the RT-LAMP-LFD was more sensitive than an existing RT-PCR method for detection of MrNV. The RT-LAMP-LFD method gave negative test results with nucleic acid extracts from normal shrimp and from shrimp infected with other viruses including DNA viruses [PstDNV (IHHNV), PemoNPV (MBV), PmDNV (HPV), WSSV] and RNA viruses (TSV, IMNV, YHV/GAV). © 2010 Elsevier Ltd.Mahidol UniversityBiochemistry, Genetics and Molecular BiologyReviewSCOPUS10.1016/j.mcp.2010.07.003