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Related Concept Videos

Investigation of Disease Outbreaks01:23

Investigation of Disease Outbreaks

Multistate foodborne outbreaks pose significant public health risks and require meticulous investigation to identify sources and implement control measures. The Centers for Disease Control and Prevention (CDC) utilizes a dynamic seven-step process for these investigations, integrating data from laboratories, interviews, and environmental assessments to protect public health.Outbreak Detection: The detection of multistate outbreaks typically begins with PulseNet, the CDC's national laboratory...
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Related Experiment Video

Updated: Jul 13, 2026

Swab Sampling Method for the Detection of Human Norovirus on Surfaces
10:03

Swab Sampling Method for the Detection of Human Norovirus on Surfaces

Published on: February 6, 2017

Probabilities in norovirus outbreak diagnosis.

Erwin Duizer1, Annemarie Pielaat, Harry Vennema

  • 1Center for Infectious Diseases Control, National Institute for Public Health and the Environment (RIVM), Bilthoven, The Netherlands. Erwin.Duizer@RIVM.NL

Journal of Clinical Virology : the Official Publication of the Pan American Society for Clinical Virology
|July 17, 2007
PubMed
Summary

Norovirus outbreaks require careful diagnosis. Testing more samples with ELISA or RT-PCR increases accuracy, with ELISA needing at least six samples for reliable norovirus detection.

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Last Updated: Jul 13, 2026

Swab Sampling Method for the Detection of Human Norovirus on Surfaces
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Detection and Genogrouping of Noroviruses from Children's Stools By Taqman One-step RT-PCR
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EPA Method 1615. Measurement of Enterovirus and Norovirus Occurrence in Water by Culture and RT-qPCR. Part III. Virus Detection by RT-qPCR
12:32

EPA Method 1615. Measurement of Enterovirus and Norovirus Occurrence in Water by Culture and RT-qPCR. Part III. Virus Detection by RT-qPCR

Published on: January 16, 2016

Area of Science:

  • Gastroenterology
  • Infectious Diseases
  • Diagnostic Microbiology

Background:

  • Noroviruses are the leading cause of acute gastroenteritis outbreaks.
  • Current diagnostic methods like RT-PCR are not widely accessible.
  • Antigen detection tests (ELISAs) are less sensitive than RT-PCR.

Purpose of the Study:

  • Establish a scientific basis for confirming norovirus as the cause of gastroenteritis outbreaks.
  • Determine optimal sample sizes for accurate norovirus outbreak diagnosis.

Main Methods:

  • Utilized binomial distribution for statistical analysis.
  • Calculated the minimum positive samples needed to confirm an outbreak.
  • Assessed the probability of detecting outbreaks with varying sample sizes and test types.

Main Results:

  • One positive sample out of 2-4 is sufficient to declare a norovirus outbreak.
  • ELISA has a low detection probability with small sample sizes (57% for 2 samples).
  • RT-PCR requires at least 3 samples, and ELISA requires 6 samples for a 90% detection probability.

Conclusions:

  • Increasing sample size from 2 to 6 significantly improves diagnostic sensitivity for both ELISA and RT-PCR.
  • ELISA can lead to false-negative outbreaks if fewer than 6 samples are tested.
  • Accurate norovirus outbreak diagnosis necessitates adequate sample sizes tailored to the chosen diagnostic method.