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논문 기본 정보

자료유형
학술저널
저자정보
In Soo Lee (Hyejeon College) Dong Hyuk Choi (Yonsei University) Jaewon Lim (Yonsei University) Yoonjung Cho (Yonsei University) Hye Sook Jeong (National Institute of Health) Doo-Sung Cheon (National Institute of Health) Hyeeun Bang (Yonsei University) Hyunwoo Jin (Yonsei University) Yeonim Choi (Yonsei University) Sangjung Park (Yonsei University) Sunghyun Kim (Yonsei University) Hyeyoung Lee (Yonsei University) Tae Ue Kim (Yonsei University)
저널정보
대한의생명과학회 대한의생명과학회지 대한의생명과학회지 제17권 제3호
발행연도
2011.9
수록면
191 - 196 (6page)

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초록· 키워드

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Noroviruses (noroV) are the major cause of nonbacterial gastroenteritis in humans worldwide. Since noroV cannot yet be cultured in vitro and their diagnosis by electron microscopy requires at least 10<sup>6</sup> viral particles/g of stool a variety of molecular detection techniques represent an important step towards the detection of noroV. In the present study, we have applied real-time nucleic acid sequence-based amplification (real-time NASBA) for simultaneous detection of NoroV genogroup Ⅰ (GⅠ) and genogroup Ⅱ (GⅡ) using standard viral RNA. For real-time NASBA assay which can detected noroV GⅠ and GⅡ, a selective region of the genes encoding the capsid protein was used to design primers and genotype-specific molecular beacon probes. The specificity of the real-time NASBA using newly designed primers and probes were confirmed using standard viral RNA of noroV GⅠ and GⅡ. To determine the sensitivity of this assay, serial 10-fold dilutions of standard viral RNA of noroV GⅠ and GⅡ were used for reverse transcription polymerase chain reaction (RT-PCR) and real-time NASBA. The results showed that while agarose gel electrophoresis could detect RT-PCR products with 10 pg of standard viral RNA, the real-time NASBA assay could detect 100 fg of standard viral RNA. These results suggested that the real-time NASBA assay has much higher sensitivity than conventional RT-PCR assay. This assay was expected that might detect the viral RNA in the specimens which could have been false negative by RT-PCR. There were needed to perform real-time NASBA with clinical specimens for evaluating accurate sensitivity and specificity of this assay.

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INTRODUCTION
MATERIALS AND METHODS
RESULTS AND DISCUSSION
REFERENCES

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UCI(KEPA) : I410-ECN-0101-2013-510-000796392