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Fast detection of Noroviruses using a real-time PCR assay and automated sample preparation

BACKGROUND: Noroviruses (NoV) have become one of the most commonly reported causative agents of large outbreaks of non-bacterial acute gastroenteritis worldwide as well as sporadic gastroenteritis in the community. Currently, reverse transcriptase polymerase chain reaction (RT-PCR) assays have been...

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Autores principales: Schmid, Michael, Oehme, Rainer, Schalasta, Gunnar, Brockmann, Stefan, Kimmig, Peter, Enders, Gisela
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC434506/
https://www.ncbi.nlm.nih.gov/pubmed/15186502
http://dx.doi.org/10.1186/1471-2334-4-15
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author Schmid, Michael
Oehme, Rainer
Schalasta, Gunnar
Brockmann, Stefan
Kimmig, Peter
Enders, Gisela
author_facet Schmid, Michael
Oehme, Rainer
Schalasta, Gunnar
Brockmann, Stefan
Kimmig, Peter
Enders, Gisela
author_sort Schmid, Michael
collection PubMed
description BACKGROUND: Noroviruses (NoV) have become one of the most commonly reported causative agents of large outbreaks of non-bacterial acute gastroenteritis worldwide as well as sporadic gastroenteritis in the community. Currently, reverse transcriptase polymerase chain reaction (RT-PCR) assays have been implemented in NoV diagnosis, but improvements that simplify and standardize sample preparation, amplification, and detection will be further needed. The combination of automated sample preparation and real-time PCR offers such refinements. METHODS: We have designed a new real-time RT-PCR assay on the LightCycler (LC) with SYBR Green detection and melting curve analysis (T(m)) to detect NoV RNA in patient stool samples. The performance of the real-time PCR assay was compared with that obtained in parallel with a commercially available enzyme immunoassay (ELISA) for antigen detection by testing a panel of 52 stool samples. Additionally, in a collaborative study with the Baden-Wuerttemberg State Health office, Stuttgart (Germany) the real-time PCR results were blindly assessed using a previously well-established nested PCR (nPCR) as the reference method, since PCR-based techniques are now considered as the "gold standard" for NoV detection in stool specimens. RESULTS: Analysis of 52 clinical stool samples by real-time PCR yielded results that were consistent with reference nPCR results, while marked differences between the two PCR-based methods and antigen ELISA were observed. Our results indicate that PCR-based procedures are more sensitive and specific than antigen ELISA for detecting NoV in stool specimens. CONCLUSIONS: The combination of automated sample preparation and real-time PCR provided reliable diagnostic results in less time than conventional RT-PCR assays. These benefits make it a valuable tool for routine laboratory practice especially in terms of rapid and appropriate outbreak-control measures in health-care facilities and other settings.
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spelling pubmed-4345062004-06-25 Fast detection of Noroviruses using a real-time PCR assay and automated sample preparation Schmid, Michael Oehme, Rainer Schalasta, Gunnar Brockmann, Stefan Kimmig, Peter Enders, Gisela BMC Infect Dis Technical Advance BACKGROUND: Noroviruses (NoV) have become one of the most commonly reported causative agents of large outbreaks of non-bacterial acute gastroenteritis worldwide as well as sporadic gastroenteritis in the community. Currently, reverse transcriptase polymerase chain reaction (RT-PCR) assays have been implemented in NoV diagnosis, but improvements that simplify and standardize sample preparation, amplification, and detection will be further needed. The combination of automated sample preparation and real-time PCR offers such refinements. METHODS: We have designed a new real-time RT-PCR assay on the LightCycler (LC) with SYBR Green detection and melting curve analysis (T(m)) to detect NoV RNA in patient stool samples. The performance of the real-time PCR assay was compared with that obtained in parallel with a commercially available enzyme immunoassay (ELISA) for antigen detection by testing a panel of 52 stool samples. Additionally, in a collaborative study with the Baden-Wuerttemberg State Health office, Stuttgart (Germany) the real-time PCR results were blindly assessed using a previously well-established nested PCR (nPCR) as the reference method, since PCR-based techniques are now considered as the "gold standard" for NoV detection in stool specimens. RESULTS: Analysis of 52 clinical stool samples by real-time PCR yielded results that were consistent with reference nPCR results, while marked differences between the two PCR-based methods and antigen ELISA were observed. Our results indicate that PCR-based procedures are more sensitive and specific than antigen ELISA for detecting NoV in stool specimens. CONCLUSIONS: The combination of automated sample preparation and real-time PCR provided reliable diagnostic results in less time than conventional RT-PCR assays. These benefits make it a valuable tool for routine laboratory practice especially in terms of rapid and appropriate outbreak-control measures in health-care facilities and other settings. BioMed Central 2004-06-09 /pmc/articles/PMC434506/ /pubmed/15186502 http://dx.doi.org/10.1186/1471-2334-4-15 Text en Copyright © 2004 Schmid et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.
spellingShingle Technical Advance
Schmid, Michael
Oehme, Rainer
Schalasta, Gunnar
Brockmann, Stefan
Kimmig, Peter
Enders, Gisela
Fast detection of Noroviruses using a real-time PCR assay and automated sample preparation
title Fast detection of Noroviruses using a real-time PCR assay and automated sample preparation
title_full Fast detection of Noroviruses using a real-time PCR assay and automated sample preparation
title_fullStr Fast detection of Noroviruses using a real-time PCR assay and automated sample preparation
title_full_unstemmed Fast detection of Noroviruses using a real-time PCR assay and automated sample preparation
title_short Fast detection of Noroviruses using a real-time PCR assay and automated sample preparation
title_sort fast detection of noroviruses using a real-time pcr assay and automated sample preparation
topic Technical Advance
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC434506/
https://www.ncbi.nlm.nih.gov/pubmed/15186502
http://dx.doi.org/10.1186/1471-2334-4-15
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