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首页> 外文期刊>Journal of Clinical Microbiology >Evaluation and Verification of the Seeplex Diarrhea-V ACE Assay for Simultaneous Detection of Adenovirus, Rotavirus, and Norovirus Genogroups I and II in Clinical Stool Specimens
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Evaluation and Verification of the Seeplex Diarrhea-V ACE Assay for Simultaneous Detection of Adenovirus, Rotavirus, and Norovirus Genogroups I and II in Clinical Stool Specimens

机译:同时检测临床凳子样本中腺病毒,轮状病毒和诺如病毒基因组I和II的Seeplex腹泻-V ACE测定法的评估和验证

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Acute viral gastroenteritis is an intestinal infection that can be caused by several different viruses. Here we describe the evaluation and verification of Seeplex Diarrhea-V ACE (Seeplex DV), a novel commercial multiplex reverse transcription-PCR (RT-PCR) assay that detects 5 diarrheal pathogens, including adenovirus, rotavirus, norovirus genogroup I (GI) and GII, and astrovirus. We describe a retrospective study of 200 clinical specimens of which 177 were stool specimens previously tested for the presence of gastrointestinal viruses by electron microscopy (EM) and/or real-time RT-PCR (rRT-PCR). The remaining 23 specimens comprised other human pathogens of viral or bacterial origin. Discordant norovirus GI and GII results were resolved using a commercial kit; discordant adenovirus and rotavirus results were resolved using a home brew multiplex rRT-PCR assay. Diagnostic sensitivities and specificities were calculated before and after discordant analysis. After discordant analysis, estimated diagnostic sensitivities were 100% for adenovirus, rotavirus, and norovirus GI and 97% for norovirus GII. Diagnostic specificities after discordant analysis were 100% for adenovirus, rotavirus, and norovirus GI and 99.4% for norovirus GII. The 95% limits of detection were 31, 10, 2, and 1 genome equivalent per reaction for adenovirus, rotavirus, and norovirus GI and GII, respectively. The results demonstrate that the Seeplex DV assay is sensitive, specific, convenient, and reliable for the simultaneous detection of several viral pathogens directly in specimens from patients with gastroenteritis. Importantly, this novel multiplex PCR assay enabled the identification of viral coinfections in 12 (6.8%) stool specimens.
机译:急性病毒性肠胃炎是一种肠道感染,可由多种不同的病毒引起。在这里,我们描述了Seeplex腹泻-V ACE(Seeplex DV)的评估和验证,Seeplex腹泻-V ACE(Seeplex DV)是一种新型的商业多重逆转录PCR(RT-PCR)分析,可检测5种腹泻病原体,包括腺病毒,轮状病毒,诺如病毒基因组I(GI)和GII和星状病毒。我们描述了一项回顾性研究,研究了200份临床标本,其中177份是粪便标本,以前曾通过电子显微镜(EM)和/或实时RT-PCR(rRT-PCR)测试过是否存在胃肠道病毒。其余23个标本包含其他人类病毒或细菌来源的病原体。使用商业试剂盒解决了不一致的诺如病毒GI和GII结果。不一致的腺病毒和轮状病毒结果使用家用自酿多重rRT-PCR分析法进行解析。在不一致分析之前和之后计算诊断敏感性和特异性。经过不一致的分析后,对于腺病毒,轮状病毒和诺如病毒GI,估计的诊断敏感性为100%,对于诺如病毒GII为97%。经不一致分析后,诊断特异性为腺病毒,轮状病毒和诺如病毒GI为100%,诺如病毒GII为99.4%。对于腺病毒,轮状病毒和诺如病毒GI和GII,每个反应的95%检测限分别为31、10、2和1个基因组当量。结果表明,Seeplex DV检测方法灵敏,特异,方便且可靠,可直接直接从胃肠炎患者的标本中同时检测多种病毒病原体。重要的是,这种新颖的多重PCR分析能够鉴定12个(6.8%)粪便标本中的病毒共感染。

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