Hepatitis E virus seroprevalence in indigenous residents of the Hà Giang northern province of Vietnam

Cover Page


Cite item

Full Text

Abstract

Vietnam is an endemic territory of the South-East Asia in terms of the prevalence of hepatitis E virus. However, the data on the prevalence of HEV infection among the indigenous population of Vietnam are limited, whereas the data on various minor ethnic groups are not available. Рopulation of the Northern province Hà Giang is characterized by ethnic diversity and consists of about 22 ethnic groups that have preserved their ethnic identity determining the features of their lifestyle and farming. The goal of the current study was to conduct a cross-sectional examination to assess prevalence of serological markers of HEV infection in the indigenous population of the Northern province of Vietnam, Hà Giang. Materials and methods. A total of 1127 healthy indigenous residents aged 18 to 83 years (average age 42.8±1.5) who lived in three regions (Yên Minh, Bắc Mê and Đông Văn) of Hà Giang province in 2019 were enrolled in the study. The presence of HEV-specific IgG antibodies (anti-HEV IgG) was determined by the ELISA using kits “DS-IFA-ANTI-HEV-G” (LLC NPO “Diagnostic Systems”, Russia). Results. The prevalence of anti-HEV IgG antibodies in the indigenous population in the Hà Giang province was 74.4% (838/1127; 95% CI 71.7–76.8), with the peak occurrence of anti-HEV IgG (87.6%) found in Đông Văn region, which was significantly higher compared to those in the Bắc Mê (χ2 = 16.37, p = 0.000052) and Yên Minh (χ2 = 214.64, p < 0.00001) regions. The Yên Minh Region was characterized by the lowest percentage of subjects involved in the epidemic process (χ2 = 77.55, p < 0.00001). No significant gender-related differences were detected in antiHEV IgG level both in general and in individual regions. The peak frequency of anti-HEV IgG (85.9%) was found in the H’mong ethnic group, which was significantly higher than in the Tay ethnic groups (χ2 = 77.32, p < 0.00001) and in the remaining minor ethnic groups (χ2 = 63.44, p < 0.00001). Conclusion. The results of this study indicate a high seroprevalence of hepatitis E virus in the minor ethnic groups, which preserve the national lifestyle in the Hà Giang province of the Northern Vietnam. As the Hà Giang province is located in remote mountain areas, a number of which are still difficult to access, its low economic status, poor sanitary and hygienic living conditions, lack of high-quality water supply, multinational population following different lifestyles, the contact of population with natural potential sources of HEV infection, including various wild and domestic animals, contribute to the successful spread of the hepatitis E virus in the region and the involvement of all populational age groups in the epidemic process. Taking into account the rapid development of the tourism industry in the Hà Giang Province particularly in the Đông Văn Region, where the Đông Văn Karst Plateau Geopark being recognized by UNESCO as national treasure is located, the results of this study emphasize a need to plan and perform the events aimed for preventing and monitoring HEV infection in endemic regions in Vietnam in order to reduce a risk of spread of hepatitis E virus not only inside, but also outside the country.

About the authors

E. V. Lichnaia

St. Petersburg Pasteur Institute

Email: evlichnaya@gmail.com
ORCID iD: 0000-0002-2835-8106

Junior Researcher, Laboratory of Molecular Epidemiology and Evolution Genetics 

St. Petersburg

Russian Federation

T.H. G. Pham

Joint Russian-Vietnamese Tropical Science and Technology Center

Email: ptgiangha@gmail.com

Researcher, Institute of Tropical Medicine 

Hanoi

Viet Nam

O. A. Petrova

St. Petersburg Pasteur Institute

Email: belka-mbf1988@mail.ru

Clinical Laboratory Diagnostics Doctor, Central Clinical and Diagnostic Laboratory 

St. Petersburg

Russian Federation

T. N. Tran

Joint Russian-Vietnamese Tropical Science and Technology Center

Email: tbnnhai@yahoo.com

Researcher, Institute of Tropical Medicine 

Hanoi

Viet Nam

T. T. Nguyen

Ha Giang CDC

Email: ptgiangha@gmail.com

MD, PhD, Director 

Hà Giang

Viet Nam

T.T. N. Bui

Joint Russian-Vietnamese Tropical Science and Technology Center

Email: ptgiangha@gmail.com

Researcher, Institute of Tropical Medicine 

Hanoi

Viet Nam

V. C. Vo

Joint Russian-Vietnamese Tropical Science and Technology Center

Email: ptgiangha@gmail.com

PhD, Deputy Director of Institute of Tropical Medicine 

Hanoi

Viet Nam

A. V. Dmitriev

Institute of Experimental Medicine

Email: admitriev@yandex.ru
ORCID iD: 0000-0002-6214-9770

PhD, MD (Biology), Professor of the Russian Academy of Sciences, Director 

St. Petersburg

Russian Federation

O. V. Kalinina

St. Petersburg Pasteur Institute

Author for correspondence.
Email: olgakalinina@mail.ru
ORCID iD: 0000-0003-1916-5705

Kalinina Olga Viktorovna,  PhD, MD (Мedicine), Professor, Head of the Molecular Epidemiology and Evolution Genetics 

197101, St. Petersburg, Mira str., 14

Phone: +7 (812) 233-21-49 

St. Petersburg

Russian Federation

References

  1. Berto A., Pham H.A., Thao T., Vy N., Caddy S.L., Hiraide R., Tue N.T., Goodfellow I., Carrique-Mas J.J., Thwaites G.E., Baker S., Boni M.F., VIZIONS consortium. Hepatitis E in southern Vietnam: seroepidemiology in humans and molecular epidemiology in pigs. Zoonoses Public Health, 2018, vol. 65, no. 1, pp. 43–50. doi: 10.1111/zph.12364
  2. Bose P.D., Das B.C., Hazam R.K., Kumar A., Medhi S., Kar P. Evidence of extrahepatic replication of hepatitis E virus in human placenta. J. Gen. Virol., 2014, vol. 95 (pt 6), pp. 1266–1271. doi: 10.1099/vir.0.063602-0
  3. Chapuy-Regaud S., Dubois M., Plisson-Chastang C., Bonnefois T., Lhomme S., Bertrand-Michel J., You B., Simoneau S., Gleizes P.E., Flan B., Abravanel F., Izopet J. Characterization of the lipid envelope of exosome encapsulated HEV particles protected from the immune response. Biochimie, 2017, vol. 141, pp. 70–79. doi: 10.1016/j.biochi.2017.05.003
  4. Công bố kết quả Tổng điều tra dân số 2019. URL: https://web.archive.org/web/20190905113157/http://tongdieutradanso.vn/congbo-ket-qua-tong-dieu-tra-dan-so-2019.html (05.07.2021)
  5. Feng Y., Feng Y.M., Wang S., Xu F., Zhang X., Zhang C., Jia Y., Yang W., Xia X., Yin J. High seroprevalence of hepatitis E virus in the ethnic minority populations in Yunnan, China. PLoS One, 2018, vol. 13, no. 5: e0197577. doi: 10.1371/journal.pone.0197577
  6. Gouilly J., Chen Q., Siewiera J., Cartron G., Levy C., Dubois M., Al-Daccak R., Izopet J., Jabrane-Ferrat N., El Costa H. Genotype specific pathogenicity of hepatitis E virus at the human maternal-fetal interface. Nat. Commun., 2018, vol. 9, no. 1: 4748. doi: 10.1038/s41467-018-07200-2
  7. Hoan N.X., Huy P.X., Sy B.T., Meyer C.G., Son T.V., Binh M.T., Giang D.P., Tu Anh D., Bock C.T., Wang B., Tong H.V., Kremsner P.G., Song L.H., Toan N.L., Velavan T.P. High hepatitis E virus (HEV) positivity among domestic pigs and risk of HEV infection of individuals occupationally exposed to pigs and pork meat in Hanoi, Vietnam. Open Forum Infect. Dis., 2019, vol. 6, no. 9: ofz306. doi: 10.1093/ofid/ofz306
  8. Hoan N.X., Tong H.V., Hecht N., Sy B.T., Marcinek P., Meyer C.G., Song, l., Toan N.L., Kurreck J., Kremsner P.G., Bock C.T., Velavan T.P. Hepatitis E virus superinfection and clinical progression in hepatitis B patients. EBioMedicine, 2015, vol. 2, no. 12, pp. 2080–2086. doi: 10.1016/j.ebiom.2015.11.020
  9. Kamar N., Izopet J., Pavio N., Aggarwal R., Labrique A., Wedemeyer H., Dalton H.R. Hepatitis E virus infection. Nat. Rev. Dis. Primers, 2017, vol. 3: 17086. doi: 10.1038/nrdp.2017.86
  10. Kamar N., Bendall R., Legrand-Abravanel F., Xia N.S., Ijaz S., Izopet J., Dalton H.R. Hepatitis E. Lancet (London, England), 2012, vol. 379, no. 9835, pp. 2477–2488. doi: 10.1016/S0140-6736(11)61849-7
  11. Khuroo M.S., Khuroo M.S., Khuroo N.S. Hepatitis E: discovery, global impact, control and cure. World J. Gastroenterol., 2016, vol. 22, no. 31, pp. 7030–7045. doi: 10.3748/wjg.v22.i31.7030
  12. Kmush B., Wierzba T., Krain L., Nelson K., Labrique A.B. Epidemiology of hepatitis E in low- and middle-income countries of Asia and Africa. Semin. Liver Dis., 2013, vol. 33, no. 1, pp. 15–29. doi: 10.1055/s-0033-1338111
  13. Kumar A., Beniwal M., Kar P., Sharma J.B., Murthy N.S. Hepatitis E in pregnancy. Int. J. Gynaecol. Obstet., 2004, vol. 85, no. 3, pp. 240–244. doi: 10.1016/j.ijgo.2003.11.018
  14. Pallerla S.R., Harms D., Johne R., Todt D., Steinmann E., Schemmerer M., Wenzel J.J., Hofmann J., Shih J., Wedemeyer H., Bock C.T., Velavan T.P. Hepatitis E virus infection: circulation, molecular epidemiology, and impact on global health. Pathogens, 2020, vol. 9, no. 10: 856. doi: 10.3390/pathogens9100856
  15. Sridhar S., Teng J.L.L., Chiu T.H., Lau S.K.P., Woo P.C.Y. Hepatitis E virus genotypes and evolution: emergence of camel hepatitis E variants. Int. J. Mol. Sci., 2017, vol. 18, no. 4: 869. doi: 10.3390/ijms18040869
  16. WHO. Hepatitis E. Fact Sheet 21 July 2020. URL: https://www.who.int/news-room/fact-sheets/detail/hepatitis-e (01.07.2021)
  17. Wu X., Chen P., Lin H., Hao X., Liang Z. Hepatitis E virus: current epidemiology and vaccine. Hum. Vaccin. Immunother., 2016, vol. 12, no. 10, pp. 2603–2610. doi: 10.1080/21645515.2016.1184806
  18. Zhang J., Zhang X.F., Huang S.J., Wu T., Hu Y.M., Wang Z.Z., Wang H., Jiang H.M., Wang Y.J., Yan Q., Guo M., Liu X.H., Li J.X., Yang C.L., Tang Q., Jiang R.J., Pan H.R., Li Y.M., Shih J.W., Ng M.H., Zhu F.C., Xia N.S. Long-term efficacy of a hepatitis E vaccine. N. Engl. J. Med. 2015, vol. 372, no. 10, pp. 914–922. doi: 10.1056/NEJMoa1406011
  19. Zhang J., Zhao Q., Xia N. Prophylactic hepatitis E vaccine. Adv. Exp. Med. Biol., 2016, vol. 948, pp. 223–246. doi: 10.1007/978-94-024-0942-0_13
  20. Zhu F.C., Zhang J., Zhang X.F., Zhou C., Wang Z.Z., Huang S.J., Wang H., Yang C.L., Jiang H.M., Cai J.P., Wang Y.J., Ai X., Hu Y.M., Tang Q., Yao X., Yan Q., Xian Y.L., Wu T., Li Y.M., Miao J., Ng M.H., Shih J.W., Xia N.S. Efficacy and safety of a recombinant hepatitis E vaccine in healthy adults: a large-scale, randomised, double-blind placebo-controlled, phase 3 trial. Lancet, 2010, vol. 376, no. 9744, pp. 895–902. doi: 10.1016/S0140-6736(10)61030-6

Supplementary files

Supplementary Files
Action
1. JATS XML

Copyright (c) 2021 Lichnaia E.V., Pham T.G., Petrova O.A., Tran T.N., Nguyen T.T., Bui T.N., Vo V.C., Dmitriev A.V., Kalinina O.V.

Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 International License.

СМИ зарегистрировано Федеральной службой по надзору в сфере связи, информационных технологий и массовых коммуникаций (Роскомнадзор).
Регистрационный номер и дата принятия решения о регистрации СМИ: серия ПИ № ФС 77 - 64788 от 02.02.2016.


This website uses cookies

You consent to our cookies if you continue to use our website.

About Cookies