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Swab Sampling Method for the Detection of Human Norovirus on Surfaces
Published on: February 6, 2017
Batch testing for noroviruses in frozen raspberries
Ann De Keuckelaere1, Dan Li1, Bart Deliens1
1Laboratory of Food Microbiology and Food Preservation, Faculty of Bioscience Engineering, Ghent University, Coupure links 653, 9000 Ghent, Belgium.
Frozen raspberries intended for puree production showed significant norovirus (NoV) contamination, indicating poor sanitary quality. Further testing is needed to assess the public health risk of these NoV findings in food products.
Area of Science:
- Food Safety
- Microbiology
- Public Health
Background:
- Raspberries are frequently linked to norovirus (NoV) outbreaks and product recalls.
- Contamination can occur in both raw materials and intermediate food products.
- Assessing viral contamination in frozen berries is crucial for food safety.
Purpose of the Study:
- To investigate the presence and levels of norovirus (GI and GII) in frozen raspberries.
- To evaluate the sanitary quality of frozen raspberries used for puree and frozen fruit mix production.
- To assess the effectiveness of sequencing for confirming RT-qPCR results.
Main Methods:
- Collected 130 frozen raspberry samples from 26 batches across four processing companies.
- Conducted enumeration of Escherichia coli and coliforms.
- Utilized real-time reverse transcription PCR (RT-qPCR) for norovirus detection (GI/GII) and sequencing for confirmation.
Main Results:
- Six of 70 samples from puree production batches tested positive for norovirus GI, with levels above the limit of quantification (4.3 log genomic copies/20g).
- Two batches were classified as having insufficient sanitary quality due to NoV presence.
- One batch of IQF raspberries tested weakly positive for NoV GI, below the limit of quantification; sequencing was successful for GI but often failed for GII.
Conclusions:
- Certain batches of frozen raspberries intended for puree production pose a sanitary quality concern due to significant norovirus contamination.
- The public health risk remains uncertain as RT-qPCR cannot distinguish between infectious and non-infectious virus particles.
- Sequencing confirmation protocols require optimization, particularly for GII norovirus detection.
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