Enteric non-A, non-B hepatitis: Epidemics, animal transmission, and hepatitis E virus detection by the polymerase chain reaction

1992 ◽  
Vol 37 (4) ◽  
pp. 263-270 ◽  
Author(s):  
Shahid Jameel ◽  
Hemlata Durgapal ◽  
C. M. Habibullah ◽  
Mohammed Sultan Khuroo ◽  
Subrat Kumar Panda
2006 ◽  
Vol 18 (5) ◽  
pp. 462-465 ◽  
Author(s):  
Salceda Fernández-Barredo ◽  
Carolina Galiana ◽  
Angel García ◽  
Santiago Vega ◽  
María Teresa Gómez ◽  
...  

1993 ◽  
Vol 59 (8) ◽  
pp. 2558-2562 ◽  
Author(s):  
N Jothikumar ◽  
K Aparna ◽  
S Kamatchiammal ◽  
R Paulmurugan ◽  
S Saravanadevi ◽  
...  

2019 ◽  
Vol 13 (1) ◽  
pp. 285-291
Author(s):  
Nashwa M. Al-Kasaby ◽  
Maysaa El Sayed Zaki

Introduction: Hepatitis E (HEV) is a major health problem affecting around one third of the world population. The prevalence of antibodies to HEV among blood donors have been documented in several countries in Europe and Asia. Objectives: The aims of the study are to estimate the seroprevalence of hepatitis E antibodies among healthy blood donors and to explore the factors associated with positive HEV antibodies among healthy blood donors. Moreover, to detect HEV viremia by real time polymerase chain reaction among seropositive blood donors for HEV. Methods: The study included 200 apparent healthy blood donors from Dakahlia Governorate, Egypt. Blood samples were collected from the blood donors for serological determination for specific hepatitis E virus immunoglobulin G (anti-HEV IgG) and specific hepatitis E virus immunoglobulin M (anti- HEV IgM). Positive samples for anti-HEV IgM were further subjected for determination of HEV-RNA by real time Polymerase Chain Reaction (PCR). Anti-HEV-IgG was positive in 50 donor (25%) anti-HEV-IgM was positive in 10 donors (5%) and HEV-RNA was positive in 6 donors (3%). Results and Discussion: The comparison between blood donors positive for anti-HEV-IgG and negative blood donors negative reveals significant association between anti-HEV-IgG and donors with older age (42.0 ± 9.7,P = 0.001),rural residence (76%, P = 0.001), workers in agricultural works (92%, P = 0.035) and elevated AST (31.28±14.28, P = 0.04). Regarding viral markers, there was significant prevalance between positive anti-HCV-IgG and positive anti-HEV-IgG (P = 0.003). Univariate analysis for risk factors associated with positive anti-HEV IgG reveals significant prevalence with older age (P = 0.001), rural residence (P < 0.001), positive anti-HCV- IgG (P = 0.004) and increase in AST (P = 0.045). However, on Multivariate analysis HEV infection was independently prevalent with older age (P < 0.001) and rural residence (P = 0.002). Conclusion: The present study highlights that HEV seroprevalence in blood donors is common finding. Further finding is the statistically significant correlation between antibodies to HCV and serological markers for HEV and even HEV viremia. Longitudinal studies may be needed to explore the clinical significance and cost effectiveness of screening of the blood donors for hepatitis E virus by serological tests and/or detection of viremia by Molecular testing.


Viruses ◽  
2020 ◽  
Vol 12 (12) ◽  
pp. 1429
Author(s):  
Radka Dziedzinska ◽  
Miroslava Krzyzankova ◽  
Marcel Bena ◽  
Petra Vasickova

Hepatitis E virus (HEV) is the etiological agent behind hepatitis E infection. Domestic pigs and wild boars are the main animal reservoirs of HEV. Very few papers describe HEV infection in goats and sheep. As the data pertaining to the presence of HEV virus in the milk of small ruminants in Europe are lacking, the aim of this paper was to examine a representative number of milk samples from these animals. The detection of HEV genome (HEV RNA) was performed using reverse transcriptase real-time polymerase chain reaction (RT-qPCR). HEV RNA was found in 2.8% of the examined samples. Positivity ranged from 101 to 103 genome equivalents/mL (GE/mL) with a median of 9.99 × 102 GE/mL. On the basis of these results, the milk of small ruminants could represent a source of HEV infection to consumers.


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