Use of internal standard RNA molecules for the RT-PCR amplification of the faeces-borne RNA viruses

被引:16
作者
Kim, K
Park, J
Chung, Y
Cheon, D
Lee, IB
Lee, S
Yoon, J
Cho, H
Song, C
Lee, KH
机构
[1] Chung Ang Univ, Coll Nat Sci, Dept Life Sci, Dongjak Ku, Seoul 156756, South Korea
[2] Natl Inst Hlth, Lab Enteroviruses, Dept Virol, Seoul 122701, South Korea
[3] Dong Shin Pharm Co Ltd, Cent Res Inst, Osan Si 447320, Kyunggi Do, South Korea
关键词
internal standard RNA; RT-PCR; faeces-borne viruses; diagnosis;
D O I
10.1016/S0166-0934(02)00016-2
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The diagnostic system based on reverse transcription (RT)-PCR has been used widely for the detection of viral genomes of faecal-borne RNA viruses. However, faecal specimens often produce both false positive and false negative results. Therefore, there is a need for a diagnosis procedure that can control for 'false-results'. In this study, an internal standard RNA that can serve as a non-competitive positive template was developed and used directly to detect faecal-borne RNA viruses without noticeable competitive inhibition of the target viral genome. These results suggest that the internal standard RNA is a useful standard molecule when undertaking diagnostic qualitative RT-PCR procedures for enteroviruses and related faecal-borne RNA viruses. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:107 / 115
页数:9
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