Abstract:After an acute hepatitis E (HEV) outbreak in Southern Switzerland, in January 2017 the local public health authorities started an active program of food chain control and public education. In this retrospective study, we analysed all laboratory-confirmed acute cases of HEV infection diagnosed between 2014 and 2020. In the period before the public health intervention, the number of cases increased steadily from 2014 (4 of 40 tests, 10%) reaching a peak in the last quarter of 2016 (42 of 285 tests, 14.7 %). Afte… Show more
“…It can therefore make a significant contribution to protecting consumers from HEV infection by improving food safety through better identification of critical control points in the processing of HEV-contaminated pork liver and through sensitive monitoring of potentially contaminated food. Further research is required to investigate the occurrence and development of the hepatitis E virus in the European food chain [24], including substantial screening of animal food stuffs, particularly pig liver, and more precise recording of the possible food-related spread. Finally, the JBH4_HEV RT-qPCR assay is a suitable tool for generating comprehensive and detailed data to fill these gaps.…”
As an international and zoonotic cause of hepatitis, hepatitis E virus (HEV) poses a significant risk to public health. However, the frequency of occurrence and the degree of contamination of food of animal origin require further research. The aim of this study was to develop and validate a highly sensitive quantitative RT-qPCR assay for the detection and quantification of HEV contamination in porcine liver and food. The focus was on genotype 3, which is most common as a food contaminant in developed countries and Europe. The selected assay has its target sequence in the open reading frame 1 (ORF1) of the HEV genome and showed good results in inclusivity testing, especially for HEV genotype 3. The developed assay seems to show high efficiency and a low intercept when compared to other assays, while having a comparable limit of detection (LOD). In addition, a standard curve was generated using artificially spiked liver to provide more accurate quantitative results for contamination assessment and tracking in this matrix. Application of the assay to test 67 pig livers from different origins resulted in a positivity rate of 7.5%, which is consistent with the results of numerous other prevalence studies. Quantitative detection of the viral genome in the food chain, particularly in pig livers, is essential for understanding the presence and evolution of HEV contamination and thus ensures consumer safety.
“…It can therefore make a significant contribution to protecting consumers from HEV infection by improving food safety through better identification of critical control points in the processing of HEV-contaminated pork liver and through sensitive monitoring of potentially contaminated food. Further research is required to investigate the occurrence and development of the hepatitis E virus in the European food chain [24], including substantial screening of animal food stuffs, particularly pig liver, and more precise recording of the possible food-related spread. Finally, the JBH4_HEV RT-qPCR assay is a suitable tool for generating comprehensive and detailed data to fill these gaps.…”
As an international and zoonotic cause of hepatitis, hepatitis E virus (HEV) poses a significant risk to public health. However, the frequency of occurrence and the degree of contamination of food of animal origin require further research. The aim of this study was to develop and validate a highly sensitive quantitative RT-qPCR assay for the detection and quantification of HEV contamination in porcine liver and food. The focus was on genotype 3, which is most common as a food contaminant in developed countries and Europe. The selected assay has its target sequence in the open reading frame 1 (ORF1) of the HEV genome and showed good results in inclusivity testing, especially for HEV genotype 3. The developed assay seems to show high efficiency and a low intercept when compared to other assays, while having a comparable limit of detection (LOD). In addition, a standard curve was generated using artificially spiked liver to provide more accurate quantitative results for contamination assessment and tracking in this matrix. Application of the assay to test 67 pig livers from different origins resulted in a positivity rate of 7.5%, which is consistent with the results of numerous other prevalence studies. Quantitative detection of the viral genome in the food chain, particularly in pig livers, is essential for understanding the presence and evolution of HEV contamination and thus ensures consumer safety.
“…To achieve a lower prevalence of HEV contamination in ready-to-eat foods in retail, it is, therefore, all the more important to monitor the spread of HEV in the pig population and the processed raw materials. Determining that the animals are HEV negative and carrying out a thorough screening of raw materials prior to and during production will most likely help to reduce HEV contamination and thus minimise infections [ 15 , 51 ].…”
Section: Discussionmentioning
confidence: 99%
“…However, as the disease hardly seems to lead to recognisable clinical symptoms in pigs [ 14 ], comprehensive screening in primary production is extremely difficult. Therefore, methods and tests for detecting HEV contaminations within the food chain and during the processing of raw materials are of great value [ 15 ].…”
In this study, changes in hepatitis E virus (HEV) contamination in the production of liver sausage from naturally contaminated pork liver were investigated. Furthermore, the potential effectiveness of individual production parameters in reducing viral loads was measured. When processing moderately contaminated liver (initial Cq-value 29), HEV RNA persisted in the finished sausages, even after heating for 90 min at 75 °C. A matrix-specific standard curve was created using a spiking experiment to accurately quantify HEV RNA in a particularly challenging matrix like liver sausage. Variations in product-specific production parameters, including mincing and heating times, showed some reduction in contamination levels, but even prolonged heating did not render all finished products HEV negative. The persistence of HEV contamination underscores the importance of ongoing monitoring in the pig population and raw materials to enhance food safety measures and reduce the likelihood of transmission through pork consumption. The detection of HEV RNA within all processing stages of pork liver in the production of liver sausage suggests that further research into the risk of infection posed by this detection and vigilance in managing HEV risks in the food chain, particularly in pork products, are required to protect public health.
“…In developed countries, including European countries, awareness of HEV infection is constantly increasing [1,2]. In Switzerland, the IgG seroprevalence of the disease is high (around 30%) [3], demanding increased awareness of the health authorities [4,5]. HEV can cause not only life-threatening acute hepatitis, but also extrahepatic manifestations [6], notably neurological diseases [7][8][9][10][11] with a tropism for the peripheral nervous system.…”
BackgroundAcute hepatitis E virus (HEV) infection recently emerged as a potential trigger for acute dysimmune neuropathies, but prospective controlled studies are lacking.AimsTo compare the frequency of concomitant acute HEV infection in patients with neuralgic amyotrophy (NA), Guillain‐Barré syndrome (GBS), and Bell's palsy with a matched control population.MethodsSwiss multicentre, prospective, observational matched case‐control study over 3 years (09.2019‐10.2022). Neurological cases with NA, GBS or Bell's palsy were recruited within 1 months from disease onset. Healthy controls were matched for age, sex, geographical location, and timing of blood collection. Diagnostic criteria for acute hepatitis E were reactive serum anti‐HEV IgM and IgG assays (ELISA test) and/or HEV RNA detection in serum by Real‐time‐PCR (RT‐PCR). RT‐PCR was performed on sera to confirm IgM positivity.ResultsWe included 180 patients (59 GBS, 51 NA, and 70 Bell's palsy cases) and corresponding matched controls (blood donors), with median age of 51 years for both groups and equal gender distribution.Six IgM+ cases were detected in the NA, two in the GBS, and none in the Bell's palsy group. Two controls were anti‐HEV IgM positive. At disease onset, most cases with acute HEV infection had increased liver enzymes. A moderate association (p=0.027; Cramér's V = ‐0.25, Fisher exact test) was observed only between acute HEV infection and NA.ConclusionThis prospective observational study suggests an association between concomitant acute HEV infection and NA, but not with GBS or Bell's palsy.
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