Yoda Tomoko, Suzuki Yasuhiko, Yamazaki Kenji, Sakon Naomi, Kanki Masashi, Aoyama Ikuko, Tsukamoto Teizo
Department of Infectious Diseases, Osaka Prefectural Institute of Public Health, Osaka, Japan.
J Med Virol. 2007 Mar;79(3):326-34. doi: 10.1002/jmv.20802.
A one-step reverse transcription loop-mediated isothermal amplification (RT-LAMP) assay for the detection of norovirus (NV) was developed. In order to design primer sets for the detection of a wide range of NVs, NVs were categorized into three groups, that is, genogroup I (GI), prevalent GII, and minor GII; three sets of primers were developed for each group. Clinical specimens of patients suffering from enteric RNA viruses, such as NV, group A and C rotavirus, and sapovirus were examined using these primer sets. Various genotypes of NVs were detected in clinical specimens from patients infected with NV where no false positive reaction was observed with other enteric RNA viruses. Additionally, 88 samples of acute gastroenteritis outbreaks were analyzed by an RT-LAMP assay and compared with the results of routine RT-PCR. The results of the RT-LAMP assay corresponded well to that of RT-PCR. These findings suggest the practical application of the RT-LAMP assay for the detection of NVs in clinical specimens. Consequently, the RT-LAMP system and conventional detection kits (NVGI and NVGII detection kits; Eiken Chemical Co., Ltd., Japan) were compared. The detection rate of the prevalent and minor GII primer sets was similar to that of the conventional NVGII kit, while the detection rate of the GI primer set is different because it can detect several genotypes better than the conventional NVGI kit. This is an initial report that the RT-LAMP system is able to detect NVs in clinical specimens within a wide range.
开发了一种用于检测诺如病毒(NV)的一步式逆转录环介导等温扩增(RT-LAMP)检测方法。为了设计用于检测多种诺如病毒的引物组,将诺如病毒分为三组,即基因群I(GI)、流行的基因群II和次要的基因群II;为每组开发了三组引物。使用这些引物组检测患有肠道RNA病毒(如诺如病毒、A组和C组轮状病毒以及札幌病毒)的患者的临床标本。在感染诺如病毒的患者的临床标本中检测到了多种基因型的诺如病毒,而未观察到与其他肠道RNA病毒的假阳性反应。此外,通过RT-LAMP检测方法分析了88份急性胃肠炎暴发样本,并与常规RT-PCR结果进行了比较。RT-LAMP检测结果与RT-PCR结果非常吻合。这些发现表明RT-LAMP检测方法在临床标本中检测诺如病毒具有实际应用价值。因此,对RT-LAMP系统和传统检测试剂盒(NVGI和NVGII检测试剂盒;日本荣化学株式会社)进行了比较。流行的和次要的基因群II引物组的检测率与传统的NVGII试剂盒相似,而基因群I引物组的检测率不同,因为它比传统的NVGI试剂盒能更好地检测几种基因型。这是关于RT-LAMP系统能够在广泛范围内检测临床标本中的诺如病毒的初步报告。