Rapid and sensitive detection of norovirus genomes in oysters by a two-step isothermal amplification assay system combining nucleic acid sequence-based amplification and reverse transcription-loop-mediated isothermal amplification assays
被引:21
作者:
Fukuda, Shinji
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Hiroshima Prefectural Technol Res Inst, Ctr Publ Hlth & Environm, Minami Ku, Hiroshima 7340007, JapanHiroshima Prefectural Technol Res Inst, Ctr Publ Hlth & Environm, Minami Ku, Hiroshima 7340007, Japan
Fukuda, Shinji
[1
]
Sasaki, Yukie
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Hiroshima Prefectural Technol Res Inst, Ctr Publ Hlth & Environm, Minami Ku, Hiroshima 7340007, JapanHiroshima Prefectural Technol Res Inst, Ctr Publ Hlth & Environm, Minami Ku, Hiroshima 7340007, Japan
Sasaki, Yukie
[1
]
Seno, Masato
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Hiroshima Prefectural Technol Res Inst, Ctr Publ Hlth & Environm, Minami Ku, Hiroshima 7340007, JapanHiroshima Prefectural Technol Res Inst, Ctr Publ Hlth & Environm, Minami Ku, Hiroshima 7340007, Japan
Seno, Masato
[1
]
机构:
[1] Hiroshima Prefectural Technol Res Inst, Ctr Publ Hlth & Environm, Minami Ku, Hiroshima 7340007, Japan
We developed a two-step isothermal amplification assay system, which achieved the detection of norovirus (NoV) genomes in oysters with a sensitivity similar to that of reverse transcription-seminested PCR. The time taken for the amplification of NoV genomes from RNA extracts was shortened to about 3 h.