- Open Access
Prevalence and risk of hepatitis E virus infection in the HIV population of Nepal
Virology Journal volume 14, Article number: 228 (2017)
Infection with the hepatitis E virus (HEV) can cause acute hepatitis in endemic areas in immune-competent hosts, as well as chronic infection in immune-compromised subjects in non-endemic areas. Most studies assessing HEV infection in HIV-infected populations have been performed in developed countries that are usually affected by HEV genotype 3. The objective of this study is to measure the prevalence and risk of acquiring HEV among HIV-infected individuals in Nepal.
We prospectively evaluated 459 Human Immunodeficiency Virus (HIV)-positive individuals from Nepal, an endemic country for HEV, for seroprevalence of HEV and assessed risk factors associated with HEV infection. All individuals were on antiretroviral therapy and healthy blood donors were used as controls.
We found a high prevalence of HEV IgG (39.4%) and HEV IgM (15.3%) in HIV-positive subjects when compared to healthy HIV-negative controls: 9.5% and 4.4%, respectively (OR: 6.17, 95% CI 4.42–8.61, p < 0.001 and OR: 3.7, 95% CI 2.35–5.92, p < 0.001, respectively). Individuals residing in the Kathmandu area showed a significantly higher HEV IgG seroprevalance compared to individuals residing outside of Kathmandu (76.8% vs 11.1%, OR: 30.33, 95% CI 18.02–51.04, p = 0.001). Mean CD4 counts, HIV viral load and presence of hepatitis B surface antigen correlated with higher HEV IgM rate, while presence of hepatitis C antibody correlated with higher rate of HEV IgG in serum. Overall, individuals with HEV IgM positivity had higher levels of alanine aminotransferase (ALT) than IgM negative subjects, suggesting active acute infection. However, no specific symptoms for hepatitis were identified.
HIV-positive subjects living in Kathmandu are at higher risk of acquiring HEV infection as compared to the general population and to HIV-positive subjects living outside Kathmandu.
Infection with the hepatitis E virus (HEV) is the most frequent cause of acute hepatitis among adults in developing countries with poor sanitation and hygiene [1, 2]. Four genotypes of the virus have been identified with different epidemiological and clinical characteristics and are capable of infecting and causing disease in human . HEV genotype 1 and 2 are restricted to human and is associated with consumption of contaminated water, which consequently leads to occasional outbreaks or sporadic acute hepatitis cases in developing countries. HEV genotypes 3 and 4 are considered zoonotic and transmission is related to consumption of raw meat products or farming. These genotypes cause sporadic acute hepatitis in industrialized nations and occasionally can progress into a chronic infection in immunosuppressed hosts [4, 5]. Nepal is an endemic region for HEV, particularly genotype 1, and repeated epidemic outbreaks have been documented since 1973 [6, 7]. Sporadic cases of acute hepatitis E occur in-between these major epidemics and account for 50% of acute hepatitis cases in the country .
The clinical course and prevalence of HEV infection in subjects infected with human immunodeficiency virus (HIV) in endemic regions has not been well established. Conflicting reports exist regarding the susceptibility to HEV infection in HIV-positive subjects from different areas of world [5, 9, 10]. Similarly, the course and severity of HEV infection in HIV-infected subjects is a matter of debate: while some studies report unrecognized self-limiting disease, others report chronic infection and rapid progression to cirrhosis [11, 12]. Nepal has nearly 40,000 people living with HIV making a prevalence rate of 0.2% amongst adults . HIV-infected persons tend to be socially marginalized and often have poor access to acceptable sanitary standards, therefore possibly being at higher risk for HEV infection. In this study, we addressed HEV infection in a cohort of HIV-infected subjects enrolled in the antiretroviral treatment program of Nepal. We explored risk factors for HEV infection in HIV-positive subjects and the relationship between immune parameters and characteristics of HEV infection.
This study was conducted among HIV-positive subjects from six districts of Nepal (Kathmandu, Lalitpur, Kaski, Sunsari, Bharatpur and Parsa) attending their respective antiretroviral therapy (ART) centers under the National ART program of Nepal, between January 2015 to March 2015. Six hundred and thirteen subjects visited the center during the study period; out of which 459 subjects were 18 years or older, and consented to participate in the study. A single time-point assessment and blood sample collection was done to obtain demographic, virological, clinical and biochemical data. Demographic and clinical data were recorded in a predesigned questionnaire. Patients with antibodies against the hepatitis C virus (HCV) were considered as co-infected irrespective of whether HCV RNA amplification was performed. A preliminary letter with some of the preliminary findings pertaining to HEV IgM was recently published by our group .
As controls, we used blood samples and demographic data of 581 healthy voluntary blood donors aged ≥18 years from the central blood bank, Kathmandu, Nepal. These blood samples were collected between February and March 2014 after informed consent for our another study to address HEV in healthy donors, and has been described in detail before . The control group constituted 401 male and 180 females. Among the screened population, 37 were from Kathmandu valley and 544 were from outside the valley. Written consent was received from all participants and the study was approved by the Nepal Health Research Council ethical review board.
Blood was collected in EDTA tubes (Becton Dickinson, USA) and CD4 counts were determined using the FACS Count system (Becton Dickinson, USA) within 3 h of collection. Similarly, samples collected in Gel clot vials were centrifuged and sera were transferred to eppendorf tubes and stored at −20° Celsius. Biochemical assays for Alanine aminotransferase (ALT), Aspartate aminotransferase (AST) and Gamma glutamyltranspeptidase (GGT) were done using Bio-Slide Technology (J&J, USA). The serology for anti-HEV IgM and anti-HEV IgG was performed using ELISA (Wantai Biological Pharmacy Enterprise, China). ELISA was undertaken in accordance with the manufacturer’s instructions. Samples with anti-HEV sample rate/cutoff rate (S/CO) ratios >1 were considered seropositive. HBsAg was assayed using Abbott-AuszymeMc (Abbott Laboratories, USA) and anti-HCV was performed by HCV ELISA (Ortho Diagnostic Systems). HIV RNA was isolated using the Nucleospin viral RNA isolation kit (MACHEREY-NAGEL, Germany) according to the manufacturer’s instruction. For viral RNA amplification and cDNA preparation artus HI Virus-1 QS-RGQ Kit (QIAGEN, Germany) was used and primers were supplied by the manufacturer as complete master mix.
The standard protocol for HEV RNA assay was adapted from previously described study by Jothikumar et al. . HEV RNA was purified from 50 μL of serum and the GenMagScript One-Step RT-PCR Kit was used for detection. The 25 μL reaction mixture contained 12.5 μL of 2X One-Step RT-PCR reaction buffer (Genmagbio, Beijing, China), 0.2 μL of GenMagScript RT Enzyme Mix, 5 μL of RNA, and primers (forward primer: BDHEVF (5′-GGTGGTT TCTGGGGTGAC-3′) and reverse primer: BDHEVR (5′-A GGGGTTGGTTGGATGAA-3′) and probe (BDHEVP; 5′-TGATTCTCAGCCCTTCGC-3′) at concentrations of 200 nM. Additionally, internal controls, supplied in the kit (GenMagScript, China), were used to identify possible PCR inhibition as detected by fluorescence channel orange in Rotor gene Q. As an exogenous internal control sequence, lambda gene PCR product (278-bp) was added to the reaction mixture.
Data was entered and analyzed using SPSS software version 23.0. Frequencies were calculated for categorical variables and mean ± SD were calculated for quantitative variables. P values of <0.05 were considered significant, unless described otherwise. Odds ratios (OR) with 95% confidence intervals were calculated. Categorical variables were compared using the chi-squared test, while the T test was used for comparing continuous variables. Spearman’s correlation coefficient was used to determine the degree of correlation between continuous variables.
Four hundred and fifty-nine HIV-positive subjects and 581 blood donors (controls) were analyzed. Their demographic profiles are presented in Table 1. Seventy of 459 (15.3%) HIV-positive subjects were reactive for anti-HEV IgM as compared to 4.4% in the HIV-negative control (blood donor) group [p < 0.001; OR: 3.7 (2.35–5.92)]. Anti-HEV IgG was positive in 181 (39.4%) of the HIV-positive subjects as compared to 56 (9.5%) of blood donors [p < 0.001; OR: 6.17 (4.42–8.61)]. Age specific prevalence rates of both anti-HEV IgM and IgG were significantly higher in HIV-infected subjects as compared to control groups for individuals younger than 20 years, between 20 and 30 years and between 31 and 40 years of age (Fig. 1). Moreover, for anti-HEV IgG, but not IgM, the prevalence rates were also significant between 41 and 50 and 51–60 years of age (Fig. 1).
We noticed a significant difference in the prevalence of anti-HEV IgG and IgM among HIV-positive study subjects living in Kathmandu, the capital of Nepal, and those residing outside of Kathmandu (Fig. 2). Overall anti-HEV IgG prevalence was 76.8% in HIV-positive subjects living in Kathmandu valley as compared to 11.1% of subjects living outside Kathmandu [p = 0.001; OR: 30.33 (18.02–51.04)]. Similarly, anti-HEV IgM was detected in 28.8% of HIV-positive subjects living in Kathmandu Valley as compared to 4.9% of those living outside Kathmandu [p = 0.001; OR: 7.71(4.07–14.58)].
We performed HEV PCR on samples of all 70 HIV-positive individuals and 27 blood donors that were positive for anti-HEV IgM. Seventeen (24%) of the HIV-positive individuals and 9 (33%) of the controls showed positive HEV RNA levels. (Table 2). The age-adjusted prevalence rates of anti-HEV IgM and anti-HEV IgG in the control group of healthy blood donors, as well as HIV-positive subjects living within Kathmandu and those living outside of Kathmandu are shown in Table 3.
Lower mean CD4 counts, higher HIV viral load (log copies), higher ALT and AST, presence of HBsAg, and living-inside-Kathmandu valley were significantly associated with a higher rate of anti-HEV IgM seropositivity, while presence of HCV antibody was significantly associated with HEV IgM seronegativity. In contrast, age, gender and duration of HIV infection were not significantly associated to anti-HEV IgM status (Table 1).
In multivariate analysis, living-inside-Kathmandu valley and anti-HCV negativity were independent risk factors associated with the presence of anti-HEV IgM positivity in HIV-infected subjects (Table 4). Interestingly, a CD4 count >200/μl, and a HIV viral load >3log copies/ml were also associated with presence of anti-HEV IgM. HIV viral load >3 log copies/ml, HCV co-infection and living-inside-the-Kathmandu valley were independent risk factors for anti-HEV IgG positivity (Table 4). The prevalence of anti-HEV IgG in HCV co-infected subjects was 47.9% as compared 13.7% in those without co-infection [p < 0.001; OR: 5.88 (3.33–10.38)] (Fig. 3).
The levels of the serum transaminases ALT and AST were also significantly higher in anti-HEV IgM positive subjects as compared to anti-HEV IgM negative HIV patients, suggesting clinically acute infection in these cases.
HEV infection is endemic in Nepal and cases occur in sporadic and epidemic fashion. The current study shows that HIV-infected individuals are at higher risk of acquiring acute HEV infection than healthy individuals in this area. Several studies from developed countries suggest that HEV is not more frequent in HIV-infected subjects compared to healthy controls [5, 10]. Kuniholm et al. reported that in the United States, HEV genotype 3 caused both acute and chronic HEV infection in HIV-positive subjects, but it was too rare to recommend routine surveillance, with only one chronic case in more than 300 tested individuals . HEV genotype 3 infection is a food-borne infection and is related to consumption of uncooked meat products. Thus, in developed countries, distribution of HEV may be determined by eating habits and methods of processing pork meat . In developing countries like Nepal, HEV is exclusively caused by genotype 1 infection [6,7,8, 17]. Contamination of the drinking water supply by HEV is common in developing nations and a large population is therefore exposed to the virus [6, 7, 18]. This likely explains the high prevalence of anti-HEV positivity in both HIV-infected as well as healthy controls in our study. However, whether HIV-infected subjects have a higher HEV attack rate as compared to the general population is not clear. HIV-infected subjects in Nepal are socially marginalized, and economically compromised . Poor access to clean drinking water could possibly explain higher anti-HEV IgM prevalence in this group regardless of their immune status.
Our study showed that anti-HEV IgG seroprevalence was higher in HIV-infected subjects as compared to the control population. Similar observations were made in Russia, Argentina and Germany [20,21,22]. However, recent studies from the United Kingdom and Spain found that anti-HEV IgG prevalence in HIV-positive and –negative subjects were not different [10, 23].Further studies are needed to understand whether this discrepancy in findings is related to HEV genotype (HEV 1 vs 3), cultural habits of the geographical region or immune status.
Although the entire country of Nepal is listed as endemic region for HEV infection, most of the major epidemics have taken place in the Kathmandu Valley. Drinking water pipelines and sewage pipelines run underground close to each other in Kathmandu Valley. A breach in sewage pipelines and subsequent fecal contamination of the water supply leads to major epidemics. Such close proximity of drinking water supply and sewage pipelines are not seen in most of the rural areas of Nepal making them less prone to outbreaks of HEV. Previous studies have demonstrated that anti-HEV IgG prevalence was high in residents of Kathmandu valley and remarkably low in other areas of Nepal . In the current study, age adjusted prevalence of anti-HEV IgG in HIV-positive subjects was 35% as compared to 8% in the control group. The prevalence of anti-HEV IgG in our study seems lower than that reported in a recent study by Izopet et al., which was conducted in a hospital of Kathmandu valley, which found 47.1% HEV seroprevalence in non-HIV-infected subjects . When we segregated our study cohort on the basis of where the subjects live, the age adjusted prevalence rate of anti-HEV IgG among HIV-positive subjects from Kathmandu was 65.8%. This value was more in concordance with that in the general population of Kathmandu as reported by Izopet et al., but still higher in HIV-infected individuals compared to controls.
The control group in our study, composed of healthy blood donors, showed an anti-HEV IgG prevalence of 8.3%, which was in the same range as previously published data from Kathmandu [25, 26], but markedly lower than Izopet et al. . This can be explained by the fact that 94% of the control group was formed by people living outside Kathmandu valley. Overall only 2% of the HIV-positive subjects living in Kathmandu lacked evidence of recent or remote infection (IgM or IgG positivity) as compared to 84.6% of subjects living outside Kathmandu. Recurrent epidemics in Kathmandu along with high prevalence of both anti-HEV IgM an IgG in subjects living in Kathmandu as compared to those living in other areas clearly indicate that HEV is largely confined to the Kathmandu valley.
In multivariate analysis, the current study identified independent risk factors for anti-HEV IgM and IgG positivity. While HIV viral load >3 log copies/ml and living in Kathmandu valley were common risk factors for anti-HEV IgM as well as IgG positivity, HCV co-infection was found to be a risk factor only for anti-HEV IgG positivity. Indeed, HCV co-infected subjects in our cohort showed a much higher evidence of immunity to HEV compared to HCV-negative (48% vs 13%). This is rather surprising since the predominant risk factor for HCV infection in Nepal is intravenous drug use. Whether intravenous drug use poses a risk for HEV exposure in HCV infected subjects leading to higher anti-HEV IgG prevalence is not known, and HEV is not known to be transmitted through blood, but it is a possibility that needs to be evaluated in future studies. Balyan et al. also reported high prevalence of anti-HEV IgG in Russian HIV-positive subjects and proposed common risk factors for transmission of both viruses . Moreover, anti-HEV IgG positivity is higher in patients undergoing hemodialysis (which is subjected to frequent blood transfusions) with no clear explanation .
It has been reported that low CD4 counts in HIV-positive patients are associated with higher anti-HEV IgG seropositivity [23, 28]. Interestingly, we observed a higher rate of anti-HEV IgM positivity in subjects with CD4 counts >200. However, one should be cautious when interpreting the immune status (i.e. the immunoglobulin levels) in immunocompromised patients. A proportion, but not all, of those that tested positive for HEV IgM showed detectable levels of HEV RNA. This could be due to a) decrease in RNA levels before negativization of IgM in acute disease or b) lack of correlation between IgM and HEV viral load. The later situation has been described before and it is thought to be due to lack of international standardization of HEV primers for PCR .
HIV-positive subjects with acute HEV infection did not show marked ALT elevations as seen in immunocompetent individuals and none of them had bilirubin >2 mg/dl. Although anti-HEV IgM positive subjects had higher ALT levels than the remaining group, the degree of ALT elevation was less than 3 times the upper limit of normal and none showed symptoms of acute hepatitis. HEV is a non-cytopathic virus and the damage of hepatocytes is an immune mediated phenomenon. Therefore, the severity of hepatocyte injury in immunocompromised hosts might be limited.
HIV-positive subjects living in Kathmandu are at higher risk of acquiring HEV infection as compared to the general population and to HIV-positive subjects living outside Kathmandu. Even though acute HEV infections are more frequently seen in HIV-positive subjects, the resulting health effects are not clear, as it does not seem to cause clinically evident disease. Further studies are necessary to understand the long-term implications of HEV infection in this population.
Hepatitis B Virus
Hepatitis C Virus
Hepatitis E virus
Human Immunodeficiency Virus
Intravenous drug user
Ahmed JA, Moturi E, Spiegel P, Schilperoord M, Burton W, Kassim NH, Mohamed A, Ochieng M, Nderitu L, Navarro-Colorado C, et al. Hepatitis E outbreak, Dadaab refugee camp, Kenya, 2012. Emerg Infect Dis. 2013;19(6):1010–2.
Kamar N, Bendall R, Legrand-Abravanel F, Xia NS, Ijaz S, Izopet J, Dalton HR. Hepatitis E. Lancet. 2012;379(9835):2477–88.
Hoofnagle JH, Nelson KE, Purcell RH. Hepatitis E. N Engl J Med. 2012;367(13):1237–44.
Dalton HR, Bendall RP, Keane FE, Tedder RS, Ijaz S. Persistent carriage of hepatitis E virus in patients with HIV infection. N Engl J Med. 2009;361(10):1025–7.
Kuniholm MH, Ong E, Hogema BM, Koppelman M, Anastos K, Peters MG, Seaberg EC, Chen Y, Nelson KE, Linnen JM. Acute and chronic hepatitis E virus infection in human immunodeficiency virus-infected U.S. women. Hepatology. 2016;63(3):712–20.
Shrestha A, Lama TK, Karki S, Sigdel DR, Rai U, Rauniyar SK, Al-Mahtab M, Takahashi K, Arai M, Akbar SM, et al. Hepatitis E epidemic, Biratnagar, Nepal, 2014. Emerg Infect Dis. 2015;21(4):711–3.
Shrestha SM. Hepatitis E in Nepal. Kathmandu Univ Med J (KUMJ). 2006;4(4):530–44.
Shrestha SM, Shrestha S, Tsuda F, Nishizawa T, Gotanda Y, Takeda N, Okamoto H. Molecular investigation of hepatitis E virus infection in patients with acute hepatitis in Kathmandu, Nepal. J Med Virol. 2003;69(2):207–14.
Jacobs C, Chiluba C, Phiri C, Lisulo MM, Chomba M, Hill PC, Ijaz S, Kelly P. Seroepidemiology of hepatitis E virus infection in an urban population in Zambia: strong association with HIV and environmental enteropathy. J Infect Dis. 2014;209(5):652–7.
Keane F, Gompels M, Bendall R, Drayton R, Jennings L, Black J, Baragwanath G, Lin N, Henley W, Ngui SL, et al. Hepatitis E virus coinfection in patients with HIV infection. HIV Med. 2012;13(1):83–8.
Neukam K, Barreiro P, Macias J, Avellon A, Cifuentes C, Martin-Carbonero L, Echevarria JM, Vargas J, Soriano V, Pineda JA. Chronic hepatitis E in HIV patients: rapid progression to cirrhosis and response to oral ribavirin. Clin Infect Dis. 2013;57(3):465–8.
Feldt T, Sarfo FS, Zoufaly A, Phillips RO, Burchard G, van Lunzen J, Jochum J, Chadwick D, Awasom C, Claussen L, et al. Hepatitis E virus infections in HIV-infected patients in Ghana and Cameroon. J Clin Virol. 2013;58(1):18–23.
Control NCfAaS: HIV epidemic update of Nepal, December 2014. 2014, http://www.ncasc.gov.np/uploaded/facts_n_figure/Factsheet-2015/Factsheet1HIVepidemicupdate_2015.pdf:1–2.
Gupta BP, Shrestha A, Adhikari A, Lama TK, Sapkota B. Acute hepatitis E virus infection in human immunodeficiency virus-positive men and women in Nepal: not quite a rare entity. Hepatology. 2016;64(3):1006–7.
Gupta BP, Lama TK, Adhikari A, Shrestha A, Rauniyar R, Sapkota B, Thapa S, Shrestha S, Gupta PP, Manandhar KD. First report of hepatitis E virus viremia in healthy blood donors from Nepal. VirusDis. 2016; doi:10.1007/s13337-016-0331-y.
Jothikumar N, Cromeans TL, Robertson BH, Meng XJ, Hill VR. A broadly reactive one-step real-time RT-PCR assay for rapid and sensitive detection of hepatitis E virus. J Virol Methods. 2006;131(1):65–71.
Shrestha SM, Shrestha S, Tsuda F, Nishizawa T, Takahashi M, Gotanda Y, Okamoto H. Genetic changes in hepatitis E virus of subtype 1a in patients with sporadic acute hepatitis E in Kathmandu, Nepal, from 1997 to 2002. J Gen Virol. 2004;85(Pt 1):97–104.
Naik SR, Aggarwal R, Salunke PN, Mehrotra NN. A large waterborne viral hepatitis E epidemic in Kanpur, India. Bull World Health Organ. 1992;70(5):597–604.
Neupane D, Khanal V, Sharma S, Aro AR. Perceived discrimination among people living with HIV in Nepal. J Nepal Health Res Counc. 2012;10(21):136–40.
Balayan MS, Fedorova OE, Mikhailov MI, Rytick PG, Eremin VF, Danilova TI, Shevelev BI, Gorbacheva EC, Pankova GY. Antibody to hepatitis E virus in HIV-infected individuals and AIDS patients. J Viral Hepat. 1997;4(4):279–83.
Fainboim H, Gonzalez J, Fassio E, Martinez A, Otegui L, Eposto M, Cahn P, Marino R, Landeira G, Suaya G, et al. Prevalence of hepatitis viruses in an anti-human immunodeficiency virus-positive population from Argentina. A multicentre study. J Viral Hepat. 1999;6(1):53–7.
Pischke S, Ho H, Urbanek F, Meyer-Olsen D, Suneetha PV, Manns MP, Stoll M, Wedemeyer H. Hepatitis E in HIV-positive patients in a low-endemic country. J Viral Hepat. 2010;17(8):598–9.
Pineda JA, Cifuentes C, Parra M, Merchante N, Perez-Navarro E, Rivero-Juarez A, Monje P, Rivero A, Macias J, Real LM. Incidence and natural history of hepatitis E virus coinfection among HIV-infected patients. AIDS. 2014;28(13):1931–7.
Izopet J, Labrique AB, Basnyat B, Dalton HR, Kmush B, Heaney CD, Nelson KE, Ahmed ZB, Zaman K, Mansuy JM, et al. Hepatitis E virus seroprevalence in three hyperendemic areas: Nepal, Bangladesh and southwest France. J Clin Virol. 2015;70:39–42.
Clayson ET, Shrestha MP, Vaughn DW, Snitbhan R, Shrestha KB, Longer CF, Innis BL. Rates of hepatitis E virus infection and disease among adolescents and adults in Kathmandu, Nepal. J Infect Dis. 1997;176(3):763–6.
Longer CF, Shrestha MP, MacArthy PO, Myint KSA, Hoke CH, Ticehurst J, Innis BL. Epidemiology of hepatitis E virus (HEV): a cohort study in Kathmandu, Nepal. In: Nishioka K, Suzuki H, Mishiro S, Oda T, editors. Viral hepatitis and liver disease: proceedings of the international symposium on viral hepatitis and liver disease: molecules today, more cures tomorrow, Tokyo, may 10–14, 1993 (1993 ISVHLD). Tokyo: Springer Japan; 1994. p. 409–11.
Harrison A, Scobie L, Crossan C, Parry R, Johnston P, Stratton J, Dickinson S, Ellis V, Hunter JG, Prescott OR, et al. Hepatitis E seroprevalence in recipients of renal transplants or haemodialysis in southwest England: a case-control study. J Med Virol. 2013;85(2):266–71.
Debes JD, Martinez Wassaf M, Pisano MB, Isa MB, Lotto M, Marianelli LG, Frassone N, Ballari E, Bohjanen PR, Hansen BE, et al. Increased hepatitis E virus Seroprevalence correlates with lower CD4+ cell counts in HIV-infected persons in Argentina. PLoS One. 2016;11(7):e0160082.
Chionne P, Madonna E, Pisani G, Taffon S, La Rosa G, Candido A, Dettori S, Tritarelli E, Equestre M, Bruni R, et al. Evaluation of rapid tests for diagnosis of acute hepatitis E. J Clin Virol. 2016;78:4–8.
The authors would like to thank all laboratory personnel, doctors, and nurses of the ART Centers.
The studies of AB are part of the Virgo consortium, funded by the Dutch government project number FES0908. JDD is partially supported by American College of Gastroenterology Clinical Research Award.
Availability of data and materials
Please contact author for data requests.
Ethics approval and consent to participate
This study was approved by the Ethical Committee of Nepal Health Research Council (NHRC). All participants gave written consent to enroll in the study. All the data and human subjects’ research were gathered and conducted for this publication under an NHRC IRB approved protocol.
Consent for publication
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.