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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...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2004
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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. |
format | Text |
id | pubmed-434506 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2004 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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