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Development and clinical validation of multiplex TaqMan® assays for rapid diagnosis of viral gastroenteritis
Author(s) -
Feeney S.A.,
Armstrong V.J.,
Mitchell S.J.,
Crawford L.,
McCaughey C.,
Coyle P.V.
Publication year - 2011
Publication title -
journal of medical virology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.782
H-Index - 121
eISSN - 1096-9071
pISSN - 0146-6615
DOI - 10.1002/jmv.22162
Subject(s) - norovirus , multiplex , rotavirus , virology , astrovirus , taqman , serotype , multiplex polymerase chain reaction , medicine , biology , virus , real time polymerase chain reaction , polymerase chain reaction , bioinformatics , biochemistry , gene
There is a need to provide rapid, sensitive, and often high throughput detection of pathogens in diagnostic virology. Viral gastroenteritis is a serious health issue often leading to hospitalization in the young, the immunocompromised and the elderly. The common causes of viral gastroenteritis include rotavirus, norovirus (genogroups I and II), astrovirus, and group F adenoviruses (serotypes 40 and 41). This article describes the work‐up of two internally controlled multiplex, probe‐based PCR assays and reports on the clinical validation over a 3‐year period, March 2007 to February 2010. Multiplex assays were developed using a combination of TaqMan™ and minor groove binder (MGB™) hydrolysis probes. The assays were validated using a panel of 137 specimens, previously positive via a nested gel‐based assay. The assays had improved sensitivity for adenovirus, rotavirus, and norovirus (97.3% vs. 86.1%, 100% vs. 87.8%, and 95.1% vs. 79.5%, respectively) and also more specific for targets adenovirus, rotavirus, and norovirus (99% vs. 95.2%, 100% vs. 93.6%, and 97.9% vs. 92.3%, respectively). For the specimens tested, both assays had equal sensitivity and specificity for astrovirus (100%). Overall the probe‐based assays detected 16 more positive specimens than the nested gel‐based assay. Post‐introduction to the routine diagnostic service, a total of 9,846 specimens were processed with multiplex 1 and 2 (7,053 pediatric, 2,793 adult) over the 3‐year study period. This clinically validated, probe‐based multiplex testing algorithm allows highly sensitive and timely diagnosis of the four most prominent causes of viral gastroenteritis. J. Med. Virol. 83:1650–1656, 2011. © 2011 Wiley‐Liss, Inc.