Quantification of hepatitis E virus in naturally-contaminated pig liver products

Hepatitis E virus (HEV), the cause of self-limiting acute hepatitis in humans, is widespread and endemic in many parts of the world. The foodborne transmission of HEV has become of concern due to the identification of undercooked pork products as a risk factor for infection. Foodborne enteric viruse...

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Main Authors: Sandra Martin-Latil, Catherine Hennechart-Collette, Sabine Delannoy, Laurent Guillier, Patrick FACH, Sylvie PERELLE
Format: Article
Language:English
Published: Frontiers Media S.A. 2016-08-01
Series:Frontiers in Microbiology
Subjects:
HEV
Online Access:http://journal.frontiersin.org/Journal/10.3389/fmicb.2016.01183/full
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spelling doaj-1634ea4df8344c16adbd88888b2eb4cd2020-11-25T01:15:08ZengFrontiers Media S.A.Frontiers in Microbiology1664-302X2016-08-01710.3389/fmicb.2016.01183204731Quantification of hepatitis E virus in naturally-contaminated pig liver productsSandra Martin-Latil0Catherine Hennechart-Collette1Sabine Delannoy2Laurent Guillier3Patrick FACH4Sylvie PERELLE5AnsesAnsesAnsesAnsesAnsesAnsesHepatitis E virus (HEV), the cause of self-limiting acute hepatitis in humans, is widespread and endemic in many parts of the world. The foodborne transmission of HEV has become of concern due to the identification of undercooked pork products as a risk factor for infection. Foodborne enteric viruses are conventionally processed by quantitative RT-PCR (RT-qPCR), which gives sensitive and quantitative detection results. Recently, digital PCR (dPCR) has been described as a novel approach to genome quantification with no need for a standard curve. The performance of microfluidic digital RT-PCR (RT-dPCR) was compared to RT-qPCR when detecting HEV in pig liver products. The sensitivity of the RT-dPCR assay was similar to that of RT-qPCR, and quantitative data obtained by both detection methods were not significantly different for almost all samples. This absolute quantification approach may be useful for standardising quantification of HEV in food samples and may be extended to quantifying other human pathogens in food samples.http://journal.frontiersin.org/Journal/10.3389/fmicb.2016.01183/fullquantificationRT-qPCRHEVPig liverRT-dPCR
collection DOAJ
language English
format Article
sources DOAJ
author Sandra Martin-Latil
Catherine Hennechart-Collette
Sabine Delannoy
Laurent Guillier
Patrick FACH
Sylvie PERELLE
spellingShingle Sandra Martin-Latil
Catherine Hennechart-Collette
Sabine Delannoy
Laurent Guillier
Patrick FACH
Sylvie PERELLE
Quantification of hepatitis E virus in naturally-contaminated pig liver products
Frontiers in Microbiology
quantification
RT-qPCR
HEV
Pig liver
RT-dPCR
author_facet Sandra Martin-Latil
Catherine Hennechart-Collette
Sabine Delannoy
Laurent Guillier
Patrick FACH
Sylvie PERELLE
author_sort Sandra Martin-Latil
title Quantification of hepatitis E virus in naturally-contaminated pig liver products
title_short Quantification of hepatitis E virus in naturally-contaminated pig liver products
title_full Quantification of hepatitis E virus in naturally-contaminated pig liver products
title_fullStr Quantification of hepatitis E virus in naturally-contaminated pig liver products
title_full_unstemmed Quantification of hepatitis E virus in naturally-contaminated pig liver products
title_sort quantification of hepatitis e virus in naturally-contaminated pig liver products
publisher Frontiers Media S.A.
series Frontiers in Microbiology
issn 1664-302X
publishDate 2016-08-01
description Hepatitis E virus (HEV), the cause of self-limiting acute hepatitis in humans, is widespread and endemic in many parts of the world. The foodborne transmission of HEV has become of concern due to the identification of undercooked pork products as a risk factor for infection. Foodborne enteric viruses are conventionally processed by quantitative RT-PCR (RT-qPCR), which gives sensitive and quantitative detection results. Recently, digital PCR (dPCR) has been described as a novel approach to genome quantification with no need for a standard curve. The performance of microfluidic digital RT-PCR (RT-dPCR) was compared to RT-qPCR when detecting HEV in pig liver products. The sensitivity of the RT-dPCR assay was similar to that of RT-qPCR, and quantitative data obtained by both detection methods were not significantly different for almost all samples. This absolute quantification approach may be useful for standardising quantification of HEV in food samples and may be extended to quantifying other human pathogens in food samples.
topic quantification
RT-qPCR
HEV
Pig liver
RT-dPCR
url http://journal.frontiersin.org/Journal/10.3389/fmicb.2016.01183/full
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