Preview

Veterinary Science Today

Advanced search

Specific prevention of duck virus hepatitis (review)

https://doi.org/10.29326/2304-196X-2026-15-2-110-122

Abstract

Introduction. Duck virus hepatitis (DVH) is a highly contagious acute disease primarily affecting ducklings, causing significant economic losses in duck farming. It is included into the World Organization for Animal Health (WOAH) list of notifiable diseases. Three main virus types cause duck virus hepatitis, with type 1 being the most ubiquitous and the primary etiological agent in most regions worldwide.

Objective. Systematization and analysis of contemporary approaches to prevention of duck virus hepatitis, review of promising strategies for recombinant and multivalent vaccine development.

Materials and methods. Literature searches and analysis were performed using the Scopus, Web of Science, Google Scholar, PubMed, ScienceDirect, and RSCI (Russian Science Citation Index) databases.

Results. This article analyzes current DVH situation, and reviews key features of the disease pathogenesis, immune response and the disease diagnosis. Furthermore, it presents comparative data on various vaccine characteristics, including production methods, efficacy, immunization schedules, immune response profiles, advantages and disadvantages, and commercial availability. This article summarizes existing approaches to livestock protection and proposes directions for further research.

Conclusion. Although a large number of different foreign vaccines against DVH is available, embryo vaccine against DVH based on VGNKI-K strain is the only vaccine produced in the Russian Federation and it has a rather limited shelf life (9 months). In response to this need, the Federal Centre for Animal Health is carrying out research aimed at developing a live freeze-dried vaccine featuring extended shelf life.

About the Authors

E. D. Kunikova
Federal Centre for Animal Health
Russian Federation

Ekaterina D. Kunikova, Leading Technologist, Laboratory for Avian Diseases Prevention

ul. Gvardeyskaya, 6, Yur’evets, Vladimir 600901



M. S. Volkov
Federal Centre for Animal Health
Russian Federation

Mikhail S. Volkov, Dr. Sci. (Veterinary Medicine), Associate Professor, Head of Laboratory for Epizootology and Monitoring

ul. Gvardeyskaya, 6, Yur’evets, Vladimir 600901



N. V. Moroz
Federal Centre for Animal Health
Russian Federation

Natalia V. Moroz, Cand. Sci. (Veterinary Medicine), Head of Laboratory for Avian Diseases Prevention

ul. Gvardeyskaya, 6, Yur’evets, Vladimir 600901



References

1. Trefilov B. B., Nikitina N. V., Iavdoshak L. I., Trubitsyn M. M. Comparative evaluation of antigenicity of live and inactivated vaccines against duck viral hepatitis type I. Veterinariya. 2019; (4): 24–27. https://doi.org/10.30896/0042-4846.2019.22.4.24-27 (in Russ.)

2. Trefilov B. B., Nikitina N. V., Dmitriev K. Yu., Trubitsyn M. M. Virusnyi gepatit utyat tipa I (epizootologiya, patogenez i diagnostika) = Duck hepatitis virus type 1 (epizootology, pathogenesis and diagnosis). Effectivnoe zhivotnovodstvo. 2017; (3): 16–17. https://elibrary.ru/zivrzn (in Russ.)

3. Niu Y., Ma H., Ding Y., Li Z., Sun Y., Li M., Shi Y. The pathogenicity of duck hepatitis A virus types 1 and 3 on ducklings. Poultry Science. 2019; 98 (12): 6333-6339. https://doi.org/10.3382/ps/pez455

4. Duck virus hepatitis. In: WOAH. Manual of Diagnostic Tests and Vaccines for Terrestrial Animals. Chapter 3.3.6. https://www.woah.org/fileadmin/Home/eng/Health_standards/tahm/3.03.06_DVH.pdf

5. Huang Q., Yue H., Zhang B., Nie P., Tang C. Development of a real-time quantitative PCR for detecting duck hepatitis A virus genotype C. Journal of Clinical Microbiology. 2012; 50 (10): 3318–3323. https://doi.org/10.1128/jcm.01080-12

6. Dmitriev K. Yu. An indirect ELISA test kit for serological diagnosis of DНV type 1: Author’s thesis for degree of Cand. Sci. (Veterinary Medicine). Saint Petersburg; 2020. 106 p. (in Russ.)

7. Bobkova G. N. Avian infectious diseases: a methodological handbook for students and practitioners. Bryansk: Bryansk State Agrarian University; 2015. 123 p. http://www.bgsha.com/ru/book/109816/ (in Russ.)

8. Leonov I. K. Biological properties of DHAV-1 vaccine strains: Author’s thesis for degree of Cand. Sci. (Veterinary Medicine). Saint Petersburg; 2018. 120 p. (in Russ.)

9. Tseng C.-H., Knowles N. J., Tsai H.-J. Molecular analysis of duck hepatitis virus type 1 indicates that it should be assigned to a new genus. Virus Research. 2007; 123 (2): 190–203. https://doi.org/10.1016/j.virusres.2006.09.007

10. Fehér E., Jakab S., Bali K., Kaszab E., Nagy B., Ihász K., et al. Genomic epidemiology and evolution of duck hepatitis A virus. Viruses. 2021; 13 (8):1592. https://doi.org/10.3390/v13081592

11. Zhang R., Xia L., Chen J., Gong Y., Zhang L., Li P., et al. Molecular epidemiology and genetic diversity of duck hepatitis A virus type 3 in Shandong province of China, 2012–2014. Acta Virologica. 2017; 61 (4): 463–472. https://doi.org/10.4149/av_2017_409

12. Doan H. T. T., Le X. T. K., Do R. T., Hoang C. T. M., Nguyen K. T., Le T. H. Molecular genotyping of duck hepatitis A viruses (DHAV) in Vietnam. The Journal of Infection in Developing Countries. 2016; 10 (9): 988–995. https://doi.org/10.3855/jidc.7239

13. Hassan T. I. R., Eid A. A. M., Ghanem I. A. I., Shahin A. M., Adael S. A. A., Mohamed F. F. First report of duck hepatitis A virus 3 from duckling flocks ofEgypt. Avian Diseases. 2020; 64 (3): 269–276. https://doi.org/10.1637/aviandiseases-d-19-00158

14. Fomenko V. Yu. Selection of systems for cultivation of duck virus hepatitis agent. Proceedings of the Federal Centre for Animal Health. 2018; 16: 424–431. https://elibrary.ru/uxvpue (in Russ.)

15. Trefilov B. B., Nikitina N. V., Yavdoshak L. I., Dmitriev K. Yu., Trubitsyn M. M. Duck hepatitis virus type 1. European Journal of Natural History. 2018; (1): 3–6. https://elibrary.ru/tbqwyh

16. Nikitina N. V., Leonov I. K., Yavdoshak L. I., Trubitsyn M. M. Duck viral hepatitis type I: a review. Ptitsevodstvo. 2023; (7–8): 74–81. https://doi.org/10.33845/0033-3239-2023-72-7-8-74-81 (in Russ.)

17. Zhang R., Yang Y., Lan J., Xie Z., Zhang X., Jiang S. Evidence of possible vertical transmission of duck hepatitis A virus type 1 in ducks. Transboundary and Emerging Diseases. 2021; 68 (2): 267–275. https://doi.org/10.1111/tbed.13708

18. Zhou S., Li S., Wang Y., Li X., Zhang T. Duck hepatitis A virus prevalence in mainland China between 2009 and 2021: a systematic review and meta-analysis. Preventive Veterinary Medicine. 2022; 208:105730. https://doi.org/10.1016/j.prevetmed.2022.105730

19. Yehia N., Erfan A. M., Omar S. E., Soliman M. A. Dual circulation of duck hepatitis A virus genotypes 1 and 3 in Egypt. Avian Diseases. 2020; 65 (1): 1–9. https://doi.org/10.1637/aviandiseases-D-20-00075

20. Rajendran R., Srinivasan J., Natarajan J., Govindan K., Kumaragurubaran K., Muthukrishnan M., et al. First report of duck hepatitis A virus genotype 2 in India. Veterinary Research Communications. 2023; 47 (3): 1231–1241. https://doi.org/10.1007/s11259-022-10063-0

21. Federal Service for Veterinary and Phytosanitary Supervision. Animal Infectious Diseases: Data from the World Organization for Animal Health (WOAH), 2024. https://fsvps.gov.ru/files/infekcionnye-bolezni-zhivotnyh-po-dannym-vozzh-2024 (in Russ.)

22. Kim S. W., Yu C. D., Park J. Y., Ma X. L., Zhu T., Li Y. F., et al. The impact of genetic variation on duck hepatitis A virus (DHAV) vaccine efficacy: a comparative study of DHAV-1 and DHAV-3 against emerging variant strains. Vaccines. 2024; 12 (12):1416. https://doi.org/10.3390/vaccines12121416

23. Mao S., Ou X., Zhu D., Chen S., Ma G., Wang M., et al. Development and evaluation of indirect ELISAs for the detection of IgG, IgM and IgA1 against duck hepatitis A virus 1. Journal of Virological Methods. 2016; 237: 79–85. https://doi.org/10.1016/j.jviromet.2016.08.019

24. Liu M., Zhang T., Zhang Y., Meng F., Li X., Hou Z., et al. Development and evaluation of a VP1-ELISA for detection of antibodies to duck hepatitis type 1 virus. Journal of Virological Methods. 2010; 169 (1): 66–69. https://doi.org/10.1016/j.jviromet.2010.06.018

25. Shen Y., Cheng A., Wang M., Chen S., Jia R., Zhu D., et al. Development of an indirect ELISA method based on the VP3 protein of duck hepatitis A virus type 1 (DHAV-1) for dual detection of DHAV-1 and DHAV-3 antibodies. Journal of Virological Methods. 2015; 225: 30–34. https://doi.org/10.1016/j.jviromet.2015.08.016

26. Chen L.-L., Xu Q., Zhang R.-H., Yang L., Li J.-X., Xie Z.-J., et al. Improved duplex RT-PCR assay for differential diagnosis of mixed infection of duck hepatitis A virus type 1 and type 3 in ducklings. Journal of Virological Methods. 2013; 192 (1–2): 12–17. https://doi.org/10.1016/j.jviromet.2013.04.012

27. Hu Q., Zhu D., Ma G., Cheng A., Wang M., Chen S., et al. A one-step duplex rRT-PCR assay for the simultaneous detection of duck hepatitis A virus genotypes 1 and 3. Journal of Virological Methods. 2016; 236: 207–214. https://doi.org/10.1016/j.jviromet.2016.07.011

28. Yun T., Ni Z., Hua J., Ye W., Chen L., Zhang S., et al. Development of a one-step real-time RT-PCR assay using a minor-groove-binding probe for the detection of duck Tembusu virus. Journal of Virological Methods. 2012; 181 (2): 148–154. https://doi.org/10.1016/j.jviromet.2012.01.019

29. Kim M. C., Kwon Y. K., Joh S. J., Kwon J. H., Lindberg A. M. Differential diagnosis between type-specific duck hepatitis virus type 1 (DHV-1) and recent Korean DHV-1-like isolates using a multiplex polymerase chain reaction. Avian Pathology. 2008; 37 (2): 171–177. https://doi.org/10.1080/03079450801918670

30. Chen X., Chen Y., Liu C., Li X., Liu H., Yin X., et al. Improved one-tube RTPCR method for simultaneous detection and genotyping of duck hepatitis A virus subtypes 1 and 3. PLoS ONE. 2019; 14 (8):e0219750. https://doi.org/10.1371/journal.pone.0219750

31. Chen L., Ma M., Zhang R., Xu Q., Si X., Wang Y., et al. Simultaneous detection of duck hepatitis A virus types 1 and 3, and of duck astrovirus type 1, by multiplex RT-PCR. Virologica Sinica. 2014; 29 (3): 196–198. https://doi.org/10.1007/s12250-014-3444-8

32. Lin S.-L., Cong R.-C., Zhang R.-H., Chen J.-H., Xia L.-L., Xie Z.-J., et al. Circulation and in vivo distribution of duck hepatitis A virus types 1 and 3 in infected ducklings. Archives of Virology. 2016; 161 (2): 405–416. https://doi.org/10.1007/s00705-015-2648-z

33. Wang Y., Zhu S., Hong W., Wang A., Zuo W. A multiplex PCR for detection of six viruses in ducks. Journal of Virological Methods. 2017; 248: 172–176. https://doi.org/10.1016/j.jviromet.2017.07.004

34. Li K. P., Ou S. C., Shien J. H., Chang P. C. Detection and differentiation of the vaccine strain and field isolates of duck hepatitis a virus type 1 using real-time RT-PCR and high-resolution melting assays. Taiwan Veterinary Journal. 2015; 41 (04): 1–7. https://doi.org/10.1142/S1682648515500146

35. Mao S., Wang M., Ou X., Sun D., Cheng A., Zhu D., et al. Virologic and immunologic characteristics in mature ducks with acute duck hepatitis A virus 1 infection. Frontiers in Immunology. 2017; 8:1574. https://doi.org/10.3389/fimmu.2017.01574

36. Zou Z., Ma J., Huang K., Chen H., Liu Z., Jin M. Live attenuated vaccine based on duck enteritis virus against duck hepatitis a virus types 1 and 3. Frontiers in Microbiology. 2016; 7:1613. https://doi.org/10.3389/fmicb.2016.01613

37. Roh J.-H., Kang M. Live attenuated duck hepatitis virus vaccine in breeder ducks: protective efficacy and kinetics of maternally derived antibodies. Veterinary Microbiology. 2018; 219: 107–112. https://doi.org/10.1016/j.vetmic.2018.04.021

38. Tsai H.-J. Duck hepatitis. In: Diseases of Poultry. Ed. by D. E. Swayne. 14th ed. Hoboken: Wiley-Blackwell; 2020; 450–459.

39. Knyazev V. P. Diseases of waterfowl. Vladimir; Pokrov; 2011. 327 p. (in Russ.)

40. Embryo vaccine against duck virus hepatitis based on strain “VGNKI-K”. https://shop.arriah.ru/catalog/vaktsiny/vaktsiny-protiv-bolezney-ptits/gepatit-utyat-zhid-shtvgnkik/?ysclid=mf11a894fp704916994 (in Russ.)

41. AVAC DVH Live (Duck viral hepatitis Vaccine). https://www.avac.com.vn/en/products-for-poultry/avacdvhlive

42. Zhang Y., Wu S., Liu W., Hu Z. Current status and future direction of duck hepatitis A virus vaccines. Avian Pathology. 2023; 52 (2): 89–99. https://doi.org/10.1080/03079457.2022.2162367

43. Kim M.-C., Kim M.-J., Kwon Y.-K., Lindberg A. M., Joh S.-J., Kwon H.-M., et al. Development of duck hepatitis A virus type 3 vaccine and its use to protect ducklings against infections. Vaccine. 2009; 27 (48): 6688–6694. https://doi.org/10.1016/j.vaccine.2009.08.092

44. Wu F., Lu F., Fan X., Pan Q., Zhao S., Sun H., et al. Development of a live attenuated duck hepatitis A virus type 3 vaccine (strain SD70). Vaccine. 2020; 38 (30): 4695–4703. https://doi.org/10.1016/j.vaccine.2020.05.030

45. Kang M., Roh J.-H., Jang H.-K. Protective efficacy of a bivalent live attenuated vaccine against duck hepatitis A virus types 1 and 3 in ducklings. Veterinary Microbiology. 2018; 214: 108–112. https://doi.org/10.1016/j.vetmic.2017.12.018

46. Gough R. E., Spackman D. Studies with inactivated duck virus hepatitis vaccines in breeder ducks. Avian Pathology. 1981. 10 (4): 471–479. https://doi.org/10.1080/03079458108418497

47. Liu X., Kong X. Isolation, identification and attenuation of a pathogenic duck hepatitis virus type 1 in China, and complete genomic sequence comparison between the embryo-passaged, attenuated derivatives and their parent. Polish Journal of Veterinary Sciences. 2019; 22 (1): 163–171. https://doi.org/10.24425/pjvs.2018.125614

48. Wang W., Said A., Wang B., Qu G., Xu Q., Liu B., Shen Z. Establishment and evaluation of the goose embryo epithelial (GEE) cell line as a new model for propagation of avian viruses. PloS ONE. 2018; 13 (3):e0193876. https://doi.org/10.1371/journal.pone.0193876

49. Wang M., Li Z., Liu H., Wang X., Zhang D. Effect of fetal calf serum on propagation of duck hepatitis A virus genotype 3 in duck embryo fibroblast cells. BMC Veterinary Research. 2019; 15 (1):153. https://doi.org/10.1186/s12917-019-1904-y

50. Wang M., Chai L., Liang S., Lv J., Yang L., Qu S., et al. Fetal calf serum exerts an inhibitory effect on replication of duck hepatitis A virus genotype 1 in duck embryo fibroblast cells. Viruses. 2020; 12 (1):80. https://doi.org/10.3390/v12010080

51. Nikitina N. V., Iavdoshak L. I., Leonov I. K., Trubitsyn M. M. Profilaktika virusnogo gepatita utyat tipa I i mery bor’by: metodicheskie polozheniya = Prevention and control of duck virus hepatitis (type 1): Methodological guidelines. Saint Petersburg: All-Russian Scientific Research Veterinary Institute of Poultry Farming; 2024. 15 p. https://elibrary.ru/fliwda (in Russ.)

52. Trefilov B. B., Nikitina N. V., Leonov I. K. The kinetics of the inactivation of the hepatitis virus type I (Avihepatovirus, Picornaviridae). Problems of Virology. 2018; 63 (3): 135–138. https://doi.org/10.18821/0507-4088-2018-63-3-135-138 (in Russ.)

53. Trefilov B. B., Nikitina N. V., Iavdoshak L. I., Trubitsyn M. M. Inactivated emulsified vaccine against viral hepatitis of ducklings type I. Veterinariya. 2018; (2): 20–23. https://elibrary.ru/yqbtfm (in Russ.)

54. Trubitsyn M. M., Nikitina N. V. The experience of using an experimental inactivated vaccine against viral hepatitis of ducklings type I. Aktual’nye problemy lecheniya i profilaktiki boleznei molodnyaka: materialy Mezhdunarodnoi nauchno-prakticheskoi konferentsii (Vitebsk, 2–4 noyabrya 2023 g.) = Current Problems in the Treatment and Prevention of Young Animal Diseases: Proceedings of the International Scientific and Practical Conference (Vitebsk, November 2–4, 2023). Vitebsk: Vitebsk the Order of “the Badge of Honor” State Academy of Veterinary Medicine; 2023; 386–389. https://elibrary.ru/urnpcf (in Russ.)

55. Nikitina N. V., Trubitsyn M. M. Experimental test of an inactivated vaccine against duck viral hepatitis A type I. Ptitsevodstvo. 2021; (12): 69–72. https://doi.org/10.33845/0033-3239-2021-70-12-69-72 (in Russ.)

56. Yin F., Li J., Zhang S., Yu M., Zhang W., Fan G., et al. Development and evaluation of an inactivated bivalent vaccine against duck viral hepatitis. Chinese Journal of Biotechnology. 2015; 31 (11): 1579–1588. https://doi.org/10.13345/j.cjb.140636 (in Chinese)

57. Zou Z., Hu Y., Liu Z., Zhong W., Cao H., Chen H., Jin M. Efficient strategy for constructing duck enteritis virus-based live attenuated vaccine against homologous and heterologous H5N1 avian influenza virus and duck enteritis virus infection. Veterinary Research. 2015; 46: 42. https://doi.org/10.1186/s13567-015-0174-3

58. Niu Y., Liu B., Sun C., Zhao L., Chen H. Construction of the recombinant duck enteritis virus delivering capsid protein VP0 of the duck hepatitis A virus. Veterinary Microbiology. 2020; 249:108837. https://doi.org/10.1016/j.vetmic.2020.108837

59. Yang F., Liu P., Li X., Liu R., Gao L., Cui H., et al. Recombinant duck enteritis virus-vectored bivalent vaccine effectively protects against duck hepatitis A virus infection in ducks. Frontiers in Microbiology. 2021; 12:813010. https://doi.org/10.3389/fmicb.2021.813010

60. Wang A. P., Liu L., Gu L. L., Guo C. M., Wu S., Feng Q., et al. Protection against duck hepatitis A virus type 1 conferred by a recombinant avian adeno-associated virus. Poultry Science. 2019; 98 (1): 112–118. https://doi.org/10.3382/ps/pey325

61. Wang A. P., Liu L., Gu L. L., Wu S., Guo C. M., Feng Q., et al. Expression of duck hepatitis A virus type 1 VP3 protein mediated by avian adeno-associated virus and its immunogenicity in ducklings. Acta Virologica. 2019; 63 (1): 53–59. https://doi.org/10.4149/av_2019_104

62. Zheng W. Q., Song M. X., Li J. L., Huang B., Li Y. F., Yu K. X., et al. Generation and evaluation of recombinant Newcastle disease viruses (NDV) expressing VP1 gene of duck hepatitis A viruses (DHAV) type 1 and 3. Chinese Journal of Veterinary Science. 2017; 37 (9): 1641–1647. https://www.cabidigitallibrary.org/doi/full/10.5555/20173348071 (in Chinese)

63. Li X., Zhao R., Lin W., Li C., Zhang T., Meng F., et al. Evidence of VP1 of duck hepatitis A type 1 virus as a target of neutralizing antibodies and involving receptor-binding activity. Virus Research. 2017; 227: 240–244. https://doi.org/10.1016/j.virusres.2016.10.018

64. Wang C., Li X. K., Wu T. C., Wang Y., Zhang C. J., Cheng X. C., Chen P. Y. Recombinant VP1 protein of duck hepatitis virus 1 expressed in Pichia pastoris and its immunogenicity in ducks. Acta Virologica. 2014; 58 (4): 333–339. https://doi.org/10.4149/av_2014_04_333

65. Truong T.-N., Cheng L.-T. Development of a subunit vaccine against duck hepatitis A virus serotype 3. Vaccines. 2022; 10 (4):523. https://doi.org/10.3390/vaccines10040523

66. Zell R., Delwart E., Gorbalenya A. E., Hovi T., King A. M. Q., Knowles N. J., et al. ICTV virus taxonomy profile: Picornaviridae. Journal of General Virology. 2017; 98 (10): 2421–2422. https://doi.org/10.1099/jgv.0.000911

67. Ku Z., Ye X., Huang X., Cai Y., Liu Q., Li Y., et al. Neutralizing antibodies induced by recombinant virus-like particles of enterovirus 71 genotype C4 inhibit infection at pre- and post-attachment steps. PLoS ONE. 2013; 8 (2):e57601. https://doi.org/10.1371/journal.pone.0057601

68. Somasundaram B., Chang C., Fan Y. Y., Lim P.-Y., Cardosa J., Lua L. Characterizing Enterovirus 71 and Coxsackievirus A16 virus-like particles production in insect cells. Methods. 2016; 95: 38–45. https://doi.org/10.1016/j.ymeth.2015.09.023

69. Marsian J., Fox H., Bahar M. W., Kotecha A., Fry E. E., Stuart D. I., et al. Plantmade polio type 3 stabilized VLPs-a candidate synthetic polio vaccine. Nature Communications. 2017; 8 (1):245. https://doi.org/10.1038/s41467-017-00090-w

70. Wang A., Gu L., Wu S., Zhu S. Duck hepatitis A virus structural proteins expressed in insect cells self-assemble into virus-like particles with strong immunogenicity in ducklings. Veterinary Microbiology. 2018; 215: 23–28. https://doi.org/10.1016/j.vetmic.2017.12.020

71. Galen. State Register of Veterinary Medicinal Products. https://galen.vetrf.ru/#/registry/pharm/registry?page=1 (in Russ.)


Supplementary files

1. Table 2. Comparative analysis of efficacy profiles of vaccine platforms
Subject
Type Исследовательские инструменты
Download (456KB)    
Indexing metadata ▾

Review

For citations:


Kunikova E.D., Volkov M.S., Moroz N.V. Specific prevention of duck virus hepatitis (review). Veterinary Science Today. 2026;15(2):110-122. (In Russ.) https://doi.org/10.29326/2304-196X-2026-15-2-110-122

Views: 89

JATS XML


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


ISSN 2304-196X (Print)
ISSN 2658-6959 (Online)