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Validation of an optimised method for quantitative detection of hepatitis E virus in pork sausage

Persson, Sofia (author)
Uppsala universitet,Infektionsmedicin
Molin, Ramia (author)
European Union Reference Laboratory for Foodborne Viruses, Swedish Food Agency, Sweden
Eriksson, Ronnie (author)
European Union Reference Laboratory for Foodborne Viruses, Swedish Food Agency, Sweden
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Lavander, Moa (author)
European Union Reference Laboratory for Foodborne Viruses, Swedish Food Agency, Sweden
Widén, Frederik (author)
Department of Microbiology, National Veterinary Institute, Sweden
Ellström, Patrik (author)
Uppsala universitet,Institutionen för medicinsk biokemi och mikrobiologi,Infektionsmedicin
Simonsson, Magnus (author)
European Union Reference Laboratory for Foodborne Viruses, Swedish Food Agency, Sweden
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 (creator_code:org_t)
English.
  • Other publication (other academic/artistic)
Abstract Subject headings
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  • Hepatitis E virus (HEV) is an emerging zoonosis that can be transmitted to humans through the consumption of raw or undercooked pork meat products. Several methods for detecting the virus in food have been described, but there are still few robust data on qualitative and quantitative performance characteristics. In this study, we developed an optimised workflow for quantitative detection of HEV in pork sausage based on a combination of previously existing protocols. The protocol uses sample disruption and phase separation with tri-reagent and 1-bromo-3-chloropropane, followed by RNA concentration with isopropanol precipitation. We validated the protocol for use on reverse transcription quantitative real-time PCR (RT-qPCR) and reverse transcription droplet digital (RT-ddPCR). The 95% limit of detection and limit of quantification was 200 copies/g for both RT-qPCR and RT-ddPCR. The RT-ddPCR technology has previously shown promise as a more precise alternative to RT-qPCR. However, we found no evidence for improved performance using RT-ddPCR instead of RT-qPCR in this method. Furthermore, we also evaluated different combinations of RNA concentration methods and PCR detection strategies. This showed that isopropanol precipitation of viral RNA was more than twice as efficient as magnetic silica bead-based extraction when an inhibitor tolerant RT-PCR detection strategy was used. In conclusion, we present an efficient and well-characterised method for quantitative detection of HEV in pork sausage. Such methods are valuable to provide high quality data for risk assessments and food monitoring.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Mikrobiologi inom det medicinska området (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Microbiology in the medical area (hsv//eng)

Keyword

HEV
real-time PCR
digital PCR
foodborne virus
validation
method characterisation
pig
wild boar
Medicinsk vetenskap
Medical Science

Publication and Content Type

vet (subject category)
ovr (subject category)

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