Cargando…

Evaluation of a Proteinase K-Based Extraction Method to Detect Hepatitis A Virus, Hepatitis E Virus and Norovirus in Artificially Contaminated Dairy Products

Human norovirus and hepatitis viruses (hepatitis A (HAV) and hepatitis E (HEV)) are leading causes of foodborne disease worldwide. Among the various food products, different types of dairy products can be implicated in viral foodborne outbreaks and contamination can occur at different stages, such a...

Descripción completa

Detalles Bibliográficos
Autores principales: Hennechart-Collette, Catherine, Fourniol, Lisa, Fraisse, Audrey, Martin-Latil, Sandra, Perelle, Sylvie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10093961/
https://www.ncbi.nlm.nih.gov/pubmed/37048310
http://dx.doi.org/10.3390/foods12071489
_version_ 1785023723275812864
author Hennechart-Collette, Catherine
Fourniol, Lisa
Fraisse, Audrey
Martin-Latil, Sandra
Perelle, Sylvie
author_facet Hennechart-Collette, Catherine
Fourniol, Lisa
Fraisse, Audrey
Martin-Latil, Sandra
Perelle, Sylvie
author_sort Hennechart-Collette, Catherine
collection PubMed
description Human norovirus and hepatitis viruses (hepatitis A (HAV) and hepatitis E (HEV)) are leading causes of foodborne disease worldwide. Among the various food products, different types of dairy products can be implicated in viral foodborne outbreaks and contamination can occur at different stages, such as preparation, contact with contaminated equipment or via other foods. The aim of this study was to characterise a proteinase K method adapted from the ISO 15216 method for the detection of HAV, HEV and norovirus in artificially contaminated dairy products, based on the recent international standard of ISO 16140-4. Results showed that the recovery yields obtained from pure RNA in dairy products ranged from 5.76% to 76.40% for HAV, from 35.09% to 100.00% for HEV, from 25.09% to 100.00% for norovirus GI and from 47.83% to 100.00% for norovirus GII. The process control MNV-1 was detected in all RNA extracts, with recovery yields between 36.83% and 100.00%. The limit of detection (LOD) of the method was between 184 and 642 genome copies/mL (or/g) for the LOD(50) and 802 and 2800 genome copies/mL or/g for the LOD(95) according to the virus analysed. This method proved to be suitable for detecting viruses in dairy products for routine diagnostic needs.
format Online
Article
Text
id pubmed-10093961
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-100939612023-04-13 Evaluation of a Proteinase K-Based Extraction Method to Detect Hepatitis A Virus, Hepatitis E Virus and Norovirus in Artificially Contaminated Dairy Products Hennechart-Collette, Catherine Fourniol, Lisa Fraisse, Audrey Martin-Latil, Sandra Perelle, Sylvie Foods Article Human norovirus and hepatitis viruses (hepatitis A (HAV) and hepatitis E (HEV)) are leading causes of foodborne disease worldwide. Among the various food products, different types of dairy products can be implicated in viral foodborne outbreaks and contamination can occur at different stages, such as preparation, contact with contaminated equipment or via other foods. The aim of this study was to characterise a proteinase K method adapted from the ISO 15216 method for the detection of HAV, HEV and norovirus in artificially contaminated dairy products, based on the recent international standard of ISO 16140-4. Results showed that the recovery yields obtained from pure RNA in dairy products ranged from 5.76% to 76.40% for HAV, from 35.09% to 100.00% for HEV, from 25.09% to 100.00% for norovirus GI and from 47.83% to 100.00% for norovirus GII. The process control MNV-1 was detected in all RNA extracts, with recovery yields between 36.83% and 100.00%. The limit of detection (LOD) of the method was between 184 and 642 genome copies/mL (or/g) for the LOD(50) and 802 and 2800 genome copies/mL or/g for the LOD(95) according to the virus analysed. This method proved to be suitable for detecting viruses in dairy products for routine diagnostic needs. MDPI 2023-04-01 /pmc/articles/PMC10093961/ /pubmed/37048310 http://dx.doi.org/10.3390/foods12071489 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Hennechart-Collette, Catherine
Fourniol, Lisa
Fraisse, Audrey
Martin-Latil, Sandra
Perelle, Sylvie
Evaluation of a Proteinase K-Based Extraction Method to Detect Hepatitis A Virus, Hepatitis E Virus and Norovirus in Artificially Contaminated Dairy Products
title Evaluation of a Proteinase K-Based Extraction Method to Detect Hepatitis A Virus, Hepatitis E Virus and Norovirus in Artificially Contaminated Dairy Products
title_full Evaluation of a Proteinase K-Based Extraction Method to Detect Hepatitis A Virus, Hepatitis E Virus and Norovirus in Artificially Contaminated Dairy Products
title_fullStr Evaluation of a Proteinase K-Based Extraction Method to Detect Hepatitis A Virus, Hepatitis E Virus and Norovirus in Artificially Contaminated Dairy Products
title_full_unstemmed Evaluation of a Proteinase K-Based Extraction Method to Detect Hepatitis A Virus, Hepatitis E Virus and Norovirus in Artificially Contaminated Dairy Products
title_short Evaluation of a Proteinase K-Based Extraction Method to Detect Hepatitis A Virus, Hepatitis E Virus and Norovirus in Artificially Contaminated Dairy Products
title_sort evaluation of a proteinase k-based extraction method to detect hepatitis a virus, hepatitis e virus and norovirus in artificially contaminated dairy products
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10093961/
https://www.ncbi.nlm.nih.gov/pubmed/37048310
http://dx.doi.org/10.3390/foods12071489
work_keys_str_mv AT hennechartcollettecatherine evaluationofaproteinasekbasedextractionmethodtodetecthepatitisavirushepatitisevirusandnorovirusinartificiallycontaminateddairyproducts
AT fourniollisa evaluationofaproteinasekbasedextractionmethodtodetecthepatitisavirushepatitisevirusandnorovirusinartificiallycontaminateddairyproducts
AT fraisseaudrey evaluationofaproteinasekbasedextractionmethodtodetecthepatitisavirushepatitisevirusandnorovirusinartificiallycontaminateddairyproducts
AT martinlatilsandra evaluationofaproteinasekbasedextractionmethodtodetecthepatitisavirushepatitisevirusandnorovirusinartificiallycontaminateddairyproducts
AT perellesylvie evaluationofaproteinasekbasedextractionmethodtodetecthepatitisavirushepatitisevirusandnorovirusinartificiallycontaminateddairyproducts