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

被引:44
作者
Higgins, Rachel R. [1 ]
Beniprashad, Melissa [1 ]
Cardona, Mark [1 ]
Masney, Steven [1 ]
Low, Donald E. [1 ,2 ,3 ]
Gubbay, Jonathan B. [1 ,2 ,3 ,4 ]
机构
[1] Ontario Agcy Hlth Protect & Promot, Toronto, ON M9P 3T1, Canada
[2] Mt Sinai Hosp, Toronto, ON M5G 1X5, Canada
[3] Univ Toronto, Toronto, ON M5S 1A1, Canada
[4] Hosp Sick Children, Toronto, ON M5G 1X8, Canada
关键词
REAL-TIME PCR; ACUTE VIRAL GASTROENTERITIS; REVERSE TRANSCRIPTION-PCR; RT-PCR; UNITED-STATES; COMMERCIAL ASSAYS; CAUSATIVE AGENTS; ENTERIC VIRUSES; HOUSE ASSAYS; GROUP-A;
D O I
10.1128/JCM.00599-11
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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.
引用
收藏
页码:3154 / 3162
页数:9
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