Preview

Veterinary Science Today

Advanced search

Improving immunoprophylaxis: potential and limitations of biotechnological solutions in Newcastle disease control

https://doi.org/10.29326/2304-196X-2026-15-2-123-130

Abstract

Introduction. Newcastle disease continues to inflict significant economic damage on the global poultry industry, dictating the need to revise traditional vaccina tion strategies. Classical live vaccines, despite their widespread use, have a number of limitations, including interference with maternal antibodies and inability to completely prevent the field virus shedding due mismatch with current genotypes. This paper constitutes an analytical review of the current landscape of genetically engineered vaccines against Newcastle disease. It systematizes the data on key technological platforms: recombinant vector vaccines, reverse genetics-based prod ucts, as well as subunit, VLP-, and DNA-vaccines. A comparative analysis of the immunogenicity, safety, and ease of use of these platforms is conducted; particular attention is paid to the possibilities of implementing the DIVA strategy. It is demonstrated that, although vector vaccines have become the industry standard, reverse genetics technologies offer unique potential for controlling viral variability and reducing virus circulation in flocks. The conclusion substantiates the need to integrate various technological approaches to create effective disease eradication programs.

Objective. Formation of an objective picture of the current state of the problem, which is necessary for determining further avenues for improving biosecurity strategies in commercial poultry farming.

Materials and methods. The analytical study was conducted on the basis of domestic and foreign scientific publications on Newcastle disease immunoprophylaxis

Results. The existing vaccines against Newcastle disease virus have been analyzed and reviewed. Their immunogenicity, ability to overcome maternal antibodies, compatibility with the DIVA strategy, virus shedding control, safety and ease of use have been described. Historical background is also provided. The necessity of transitioning from traditional vaccines to genetically engineered prophylactic products is substantiated.

Conclusion. The development and implementation of subunit and nucleic acid vaccines are the most important evolutionary steps in the field of Newcastle disease immunoprophylaxis, thus enabling the implementation of the virus eradication strategy in poultry flocks.

About the Authors

T. A. Bairashev
Federal Center for Toxicological, Radiation and Biological Safety
Russian Federation

Timur A. Bairashev, Postgraduate Student, Junior Researcher, Laboratory for Viral Anthropozoonoses

Nauchnyi gorodok-2, Kazan 420075, Republic of Tatarstan



A. G. Galeeva
Federal Center for Toxicological, Radiation and Biological Safety; Kazan State Agrarian University, Kazan State Academy of Veterinary Medicine named after N. E. Bauman
Russian Federation

Antonina G. Galeeva, Cand. Sci. (Veterinary Medicine), Leading Researcher, Laboratory for Viral Anthropozoonoses

Nauchnyi gorodok-2, Kazan 420075, Republic of Tatarstan

ul. Sibirskii Tract 35, Kazan 420029, Republic of Tatarstan



M. A. Efimova
Federal Center for Toxicological, Radiation and Biological Safety; Kazan State Agrarian University, Kazan State Academy of Veterinary Medicine named after N. E. Bauman
Russian Federation

Marina A. Efimova, Dr. Sci. (Biology), Leading Researcher, Laboratory for Viral Anthropozoonoses

Nauchnyi gorodok-2, Kazan 420075, Republic of Tatarstan

ul. Sibirskii Tract 35, Kazan 420029, Republic of Tatarstan



References

1. Ariyama N., Tapia R., Godoy C., Agüero B., Valdés V., Berrios F., et al. Avian orthoavulavirus 1 (Newcastle disease virus) antibodies in five penguin species, Antarctic peninsula and Southern Patagonia. Transboundary and Emerging Diseases. 2021; 68 (6): 3096–3102. https://doi.org/10.1111/tbed.14037

2. Mao Q., Ma S., Schrickel P. L., Zhao P., Wang J., Zhang Y., et al. Review detection of Newcastle disease virus. Frontiers in Veterinary Science. 2022; 9:936251. https://doi.org/10.3389/fvets.2022.936251

3. Charkhkar S., Bashizade M., Sotoudehnejad M., Ghodrati M., Bulbuli F., Akbarein H. The evaluation and importance of Newcastle disease’s economic loss in commercial layer poultry. Journal of Poultry Sciences and Avian Diseases. 2024; 2 (1): 1–4. https://doi.org/10.61838/kman.jpsad.2.1.1

4. Хлып Д. Н. Болезнь Ньюкасла. БИО. 2021; (1): 5–20. https://elibrary.ru/uspbuhKhlyp D. N. Bolezn’ N’yukasla = Newcastle disease. BIO. 2021; (1): 5–20. https://elibrary.ru/uspbuh (in Russ.)

5. Kondakova O. A., Agranovsky A. A., Ryabchevskaya E. M., Umarova E. P., Granovskiy D. L., Toropov S. E., et al. Genetic diversity of Newcastle disease virus and its implications for vaccine development. Veterinary Sciences. 2025; 12 (9):858. https://doi.org/10.3390/vetsci12090858

6. Bello M. B., Yusoff K., Ideris A., Hair-Bejo M., Peeters B. P. H., Omar A. R. Diagnostic and vaccination approaches for Newcastle disease virus in poultry: the current and emerging perspectives. BioMed Research International. 2018; 2018:7278459. https://doi.org/10.1155/2018/7278459

7. Winterfield R. W., Dhillon A. S., Alby L. J. Vaccination of chickens against Newcastle disease with live and inactivated Newcastle disease virus. Poultry Science. 1980; 59 (2): 240–246. https://doi.org/10.3382/ps.0590240

8. Hitchner S. B., Reising G., Van Roeke H. Characteristics of the B1 strain of Newcastle disease virus. American Journal of Veterinary Research. 1951; 12 (44): 246–249. https://pubmed.ncbi.nlm.nih.gov/14847122/

9. Winterfield R. W., Goldman C. L., Seadale E. H. Newcastle disease immunization studies: 4. Vaccination of chickens with B1, F and LaSota strains of Newcastle disease virus administered through drinking water. Poultry Science. 1957; 36 (5): 1076–1088. https://doi.org/10.3382/ps.0361076

10. Roohani K., Tan S. W., Yeap S. K., Ideris A., Bejo M. H., Omar A. R. Characterisation of genotype VII Newcastle disease virus (NDV) isolated from NDV vaccinated chickens, and the efficacy of LaSota and recombinant genotype VII vaccines against challenge with velogenic NDV. Journal of Veterinary Science. 2015; 16 (4): 447–457. https://doi.org/10.4142/jvs.2015.16.4.447

11. Dimitrov K. M., Abolnik C., Afonso C. L., Albina E., Bahl J., Berg M., et al. Updated unified phylogenetic classification system and revised nomenclature for Newcastle disease virus. Infection, Genetics and Evolution. 2019; 74:103917. https://doi.org/10.1016/j.meegid.2019.103917

12. Bello M. B., Yusoff K., Ideris A., Hair-Bejo M., Jibril A. H., Peeters B. P. H., Omar A. R. Exploring the prospects of engineered Newcastle disease virus in modern vaccinology. Viruses. 2020; 12 (4):451. https://doi.org/10.3390/v12040451

13. Hu Z., He X., Deng J., Hu J., Liu X. Current situation and future direction of Newcastle disease vaccines. Veterinary Research. 2022; 53 (1):99. https://doi.org/10.1186/s13567-022-01118-w

14. Lancaster J. E. Newcastle disease: a review of some of the literature published between 1926 and 1964. Monograph No. 3. Ottawa: Canada Department of Agriculture; 1966. 188 p.

15. Alexander D. J., Aldous E. W., Fuller C. M. The long view: a selective review of 40 years of Newcastle disease research. Avian Pathology. 2012; 41 (4): 329–335. https://doi.org/10.1080/03079457.2012.697991

16. Hu Z., Ni J., Cao Y., Liu X. Newcastle disease virus as a vaccine vector for 20 years: a focus on maternally derived antibody interference. Vaccines. 2020; 8 (2):222. https://doi.org/10.3390/vaccines8020222

17. Millar N. S., Emmerson P. T. Molecular cloning and nucleotide sequencing of Newcastle disease virus. In: Newcastle Disease. Ed. by D. J. Alexander. Developments in Veterinary Virology. Vol. 8. Boston: Springer; 1988; Chapter 5: 79–97. https://doi.org/10.1007/978-1-4613-1759-3_5

18. Boyle D. B., Heine H. G. Recombinant fowlpox virus vaccines for poultry. Immunology and Cell Biology. 1993; 71 (5): 391–397. https://doi.org/10.1038/icb.1993.45

19. Boursnell M. E., Green P. F., Campbell J. I., Deuter A., Peters R. W., Tomley F. M., et al. Insertion of the fusion gene from Newcastle disease virus into a non-essential region in the terminal repeats of fowlpox virus and demonstration of protective immunity induced by the recombinant. Journal of General Virology. 1990; 71 (3): 621–628. https://doi.org/10.1099/0022-1317-71-3-621

20. Taylor J., Christensen L., Gettig R., Goebel J., Bouquet J.-F., Mickle T. R., Paoletti E. Efficacy of a recombinant fowl pox-based Newcastle disease virus vaccine candidate against velogenic and respiratory challenge. Avian Diseases. 1996; 40 (1): 173–180. https://doi.org/10.2307/1592386

21. Wang H., Tian J., Zhao J., Zhao Y., Yang H., Zhang G. Current status of poultry recombinant virus vector vaccine development. Vaccines. 2024; 12 (6):630. https://doi.org/10.3390/vaccines12060630

22. Heckert R. A., Riva J., Cook S., McMillen J., Schwartz R. D. Onset of protective immunity in chicks after vaccination with a recombinant herpesvirus of turkeys vaccine expressing Newcastle disease virus fusion and hemagglutinin-neuraminidase antigens. Avian Diseases. 1996; 40 (4): 770–777. https://doi.org/10.2307/1592296

23. Morgan R. W., Gelb J. Jr., Pope C. R., Sondermeijer P. J. A. Efficacy in chickens of a herpesvirus of turkeys recombinant vaccine containing the fusion gene of Newcastle disease virus: onset of protection and effect of maternal antibodies. Avian Diseases. 1993; 37 (4): 1032–1040. https://doi.org/10.2307/1591910

24. Sondermeijer P. J., Claessens J. A. J., Jenniskens P. E., Mockett A. P., Thijssen R. A. J., Willemse M. J., Morgan R. W. Avian herpesvirus as a live viral vector for expression of heterologous antigens. Vaccine. 1993; 11 (3): 349–358. https://doi.org/10.1016/0264-410X(93)90198-7

25. Hu Z., Liu X. “Antigen camouflage and decoy” strategy to overcome interference from maternally derived antibody with Newcastle disease virusvectored vaccines: more than a simple combination. Frontiers in Microbiology. 2021; 12:735250. https://doi.org/10.3389/fmicb.2021.735250

26. Rauw F., Gardin Y., Palya V., Anbari S., Lemaire S., Boschmans M., et al. Improved vaccination against Newcastle disease by an in ovo recombinant HVT-ND combined with an adjuvanted live vaccine at day-old. Vaccine. 2010; 28 (3): 823–833. https://doi.org/10.1016/j.vaccine.2009.10.049

27. Cardenas-Garcia S., Afonso C. L. Reverse genetics of Newcastle disease virus. In: Reverse Genetics of RNA Viruses. Ed. by D. Perez. Methods in Molecular Biology. Vol. 1602. New York: Humana Press; 2017; Chapter 10: 141–158. https://doi.org/10.1007/978-1-4939-6964-7_10

28. Peeters B. P., de Leeuw O. S., Koch G., Gielkens A. L. Rescue of Newcastle disease virus from cloned cDNA: evidence that cleavability of the fusion protein is a major determinant for virulence. Journal of Virology. 1999; 73 (6): 5001–5009. https://doi.org/10.1128/JVI.73.6.5001-5009.1999

29. Römer-Oberdörfer A., Mundt E., Mebatsion T., Buchholz U. J., Mettenleiter T. C. Generation of recombinant lentogenic Newcastle disease virus from cDNA. Journal of General Virology. 1999; 80 (11): 2987–2995. https://doi.org/10.1099/0022-1317-80-11-2987

30. Römer-Oberdörfer A., Werner O., Veits J., Mebatsion T., Mettenleiter T. C. Contribution of the length of the HN protein and the sequence of the F protein cleavage site to Newcastle disease virus pathogenicity. Journal of General Virology. 2003; 84 (11): 3121–3129. https://doi.org/10.1099/vir.0.19416-0

31. Palya V., Kiss I., Tatár-Kis T., Mató T., Felföldi B., Gardin Y. Advancement in vaccination against Newcastle disease: recombinant HVT NDV provides high clinical protection and reduces challenge virus shedding with the absence of vaccine reactions. Avian Diseases. 2012; 56 (2): 282–287. https://doi.org/10.1637/9935-091511-Reg.1

32. Rauw F., Ngabirano E., Gardin Y., Palya V., Lambrecht B. Effectiveness of a simultaneous rHVT-F(ND) and rHVT-H5(AI) vaccination of day-old chickens and the influence of NDV- and AIV-specific MDA on immune response and conferred protection. Vaccines. 2020; 8 (3):536. https://doi.org/10.3390/vaccines8030536

33. Lee J., Lee C.-W., Suarez D. L., Lee S. A., Kim T., Spackman E. Efficacy of commercial recombinant HVT vaccines against a North American clade 2.3.4.4b H5N1 highly pathogenic avian influenza virus in chickens. PLoS ONE. 2024; 19 (7):e0307100. https://doi.org/10.1371/journal.pone.0307100

34. Shafaati M., Ebadi M., Ghorbani M. A short review of progress in development of Newcastle disease vaccines. Journal of Veterinary Medicine and Research. 2022; 9 (2):1231. https://www.jscimedcentral.com/public/assets/articles/veterinarymedicine-9-1231.pdf

35. Sun H.-L., Wang Y.-F., Tong G.-Z., Zhang P.-J., Miao D.-Y., Zhi H.-D., et al. Protection of chickens from Newcastle disease and infectious laryngotracheitis with a recombinant fowlpox virus co-expressing the F, HN genes of Newcastle disease virus and gB gene of infectious laryngotracheitis virus. Avian Diseases. 2008; 52 (1): 111–117. https://doi.org/10.1637/7998-041807-reg

36. Dimitrov K. M., Afonso C. L., Yu Q., Miller P. J. Newcastle disease vaccines – a solved problem or a continuous challenge? Veterinary Microbiology. 2017; 206: 126–136. https://doi.org/10.1016/j.vetmic.2016.12.019

37. Newcastle disease (infection with Newcastle disease virus). Chapter 3.3.14. In: WOAH. Manual of Diagnostic Tests and Vaccines for Terrestrial Animals (mammals, birds and bees). https://www.woah.org/fileadmin/Home/eng/Health_standards/tahm/3.03.10_NEWCASTLE_DIS.pdf

38. Lan T., Liu Q., Ge J., Wang Y. A novel approach for efficient co-expression of two foreign genes based on the reverse genetic system of Newcastle disease virus. Frontiers in Microbiology. 2024; 15:1442551. https://doi.org/10.3389/fmicb.2024.1442551

39. Hu S., Ma H., Wu Y., Liu W., Wang X., Liu Y., Liu X. A vaccine candidate of attenuated genotype VII Newcastle disease virus generated by reverse genetics. Vaccine. 2009; 27 (6): 904–910. https://doi.org/10.1016/j.vaccine.2008.11.091

40. Tavassoli A., Soleymani S., Haghparast A., Hashemi Tabar G., Bassami M. R., Dehghani H. Reverse genetics assembly of Newcastle disease virus genome template using Asis-Sal-Pac BioBrick strategy. Biological Procedures Online. 2020; 22:9. https://doi.org/10.1186/s12575-020-00119-3

41. Amoia C. F., Chengula A. A., Hakizimana J. N., Wambura P. N., Munir M., Misinzo G., Weger-Lucarelli J. Development of a genotype-matched Newcastle disease DNA vaccine candidate adjuvanted with IL-28b for the control of targeted velogenic strains of Newcastle disease virus in Africa. Veterinary Research Communications. 2025; 49 (1):33. https://doi.org/10.1007/s11259-024-10590-y

42. Mebatsion T., Koolen M. J., de Vaan L. T., de Haas N., Braber M., RömerOberdörfer A., et al. Newcastle disease virus (NDV) marker vaccine: an immunodominant epitope on the nucleoprotein gene of NDV can be deleted or replaced by a foreign epitope. Journal of Virology. 2002; 76 (20): 1013810146. https://doi.org/10.1128/JVI.76.20.10138-10146.2002

43. Pasick J. Application of DIVA vaccines and their companion diagnostic tests to foreign animal disease eradication. Animal Health Research Reviews. 2004; 5 (2): 257–262. https://doi.org/10.1079/AHR200479

44. Milić N., Nišavić J., Zorić A., Krnjaić D., Radojičić M., Stanojković A. Overview of current advances in the development of subunit and recombinant vaccines against Newcastle disease virus. Biotechnology in Animal Husbandry. 2017; 33 (1): 1–11. https://doi.org/10.2298/BAH1701001M

45. Wang N., Huang M., Fung T. S., Luo Q., Ye J. X., Du Q. R., et al. Rapid development of an effective Newcastle disease virus vaccine candidate by attenuation of a genotype VII velogenic isolate using a simple infectious cloning system. Frontiers in Veterinary Science. 2020; 7:648. https://doi.org/10.3389/fvets.2020.00648

46. Bobbala S., Hook S. Is there an optimal formulation and delivery strategy for subunit vaccines? Pharmaceutical Research. 2016; 33 (9): 20782097. https://doi.org/10.1007/s11095-016-1979-0

47. Wang J., Lan Q., Zong X., Zhu G., Yang R., Yang G., et al. Protection against genotype VII Newcastle disease virus by a mucosal subunit vaccination based on bacterium-like particles bearing the F or HN antigen. International Journal of Biological Macromolecules. 2023; 244:125293. https://doi.org/10.1016/j.ijbiomac.2023.125293

48. Park J. K., Lee D. H., Yuk S. S., Tseren-Ochir E. O., Kwon J. H., Noh J. Y., et al. Virus-like particle vaccine confers protection against a lethal Newcastle disease virus challenge in chickens and allows a strategy of differentiating infected from vaccinated animals. Clinical and Vaccine Immunology. 2014; 21 (3): 360–365. https://doi.org/10.1128/CVI.00636-13

49. Choi K.-S., Kye S.-J., Jeon W.-J., Park M.-J., Kim S., Seul H.-J., Kwon J.-H. Preparation and diagnostic utility of a hemagglutination inhibition test antigen derived from the baculovirus-expressed hemagglutinin-neuraminidase protein gene of Newcastle disease virus. Journal of Veterinary Science. 2013; 14 (3): 291–297. https://doi.org/10.4142/jvs.2013.14.3.291

50. Shahid N., Rao A. Q., Ahad A., Gul A., Latif A., Azam S., et al. E. coli expression and immunological assessment of expressed recombinant Newcastle disease virus hemagglutinin-neuraminidase protein in chickens. Acta Virologica. 2020; 64 (3): 331–337. https://doi.org/10.4149/av_2020_310

51. Kang X., Wang J., Jiao Y., Tang P., Song L., Xiong D., et al. Expression of recombinant Newcastle disease virus F protein in Pichia pastoris and its immunogenicity using flagellin as the adjuvant. Protein Expression and Purification. 2016; 128: 73–80. https://doi.org/10.1016/j.pep.2016.08.009

52. Baradaran A., Yusoff K., Shafee N., Rahim R. A. Newcastle disease virus hemagglutinin-neuraminidase as a potential cancer targeting agent. Journal of Cancer. 2016; 7 (4): 462–466. https://doi.org/10.7150/jca.13566

53. Berinstein A., Vazquez-Rovere C., Asurmendi S., Gómez E., Zanetti F., Zabal O., et al. Mucosal and systemic immunization elicited by Newcastle disease virus (NDV) transgenic plants as antigens. Vaccine. 2005; 23 (48–49): 5583–5589. https://doi.org/10.1016/j.vaccine.2005.06.033

54. Lu B., Lim J. M., Yu B., Song S., Neeli P., Sobhani N., et al. The nextgeneration DNA vaccine platforms and delivery systems: advances, challenges and prospects. Frontiers in Immunology. 2024; 15:1332939. https://doi.org/10.3389/fimmu.2024.1332939

55. Porter K. R., Raviprakash K. DNA vaccine delivery and improved immunogenicity. Current Issues in Molecular Biology. 2017; 22: 129–138. https://doi.org/10.21775/cimb.022.129

56. Zhao Z., Ma X., Zhang R., Hu F., Zhang T., Liu Y., et al. A novel liposomepolymer hybrid nanoparticles delivering a multi-epitope self-replication DNA vaccine and its preliminary immune evaluation in experimental animals. Nanomedicine: Nanotechnology, Biology and Medicine. 2021; 35:102338. https://doi.org/10.1016/j.nano.2020.102338

57. Thirumalaikumar E., Vimal S., Sathishkumar R., Ravi M., Karthick V., Ramya S., et al. DNA vaccine incorporated poly (lactic-co-glycolic) acid (PLGA) microspheres offer enhanced protection against Aeromonas hydrophila infection. International Journal of Biological Macromolecules. 2023; 253 (5):127182. https://doi.org/10.1016/j.ijbiomac.2023.127182

58. Yang X., Yuan X., Cai D., Wang S., Zong L. Low molecular weight chitosan in DNA vaccine delivery via mucosa. International Journal of Pharmaceutics. 2009; 375 (1–2): 123–132. https://doi.org/10.1016/j.ijpharm.2009.03.032

59. Фролов С. В., Мороз Н. В., Чвала И. А., Ирза В. Н. Эффективность вакцин против ньюкаслской болезни производства ФГБУ «ВНИИЗЖ» в отношении актуальных вирусов VII генотипа. Ветеринария сегодня. 2021; (1): 44–51. https://doi.org/10.29326/2304-196X-2021-1-36-44-51Frolov S. V., Moroz N. V., Chvala I. A., Irza V. N. Effectiveness of vaccines produced by the Federal State-Financed Institution “ARRIAH” against topical genotype VII Newcastle disease viruses. Veterinary Science Today. 2021; (1): 44–51. https://doi.org/10.29326/2304-196X-2021-1-36-44-51

60. Miller P. J., Afonso C. L., El Attrache J., Dorsey K. M., Courtney S. C., Guo Z., Kapczynski D. R. Effects of Newcastle disease virus vaccine antibodies on the shedding and transmission of challenge viruses. Developmental and Comparative Immunology. 2013; 41 (4): 505–513. https://doi.org/10.1016/j.dci.2013.06.007

61. Izquierdo-Lara R., Chumbe A., Calderón K., Fernández-Díaz M., Vakharia V. N. Genotype-matched Newcastle disease virus vaccine confers improved protection against genotype XII challenge: the importance of cytoplasmic tails in viral replication and vaccine design. PLoS ONE. 2019; 14 (11):e0209539. https://doi.org/10.1371/journal.pone.0209539

62. Lee Y.-J., Sung H.-W., Choi J.-G., Lee E.-K., Yoon H., Kim J.-H., Song C.-S. Protection of chickens from Newcastle disease with a recombinant baculovirus subunit vaccine expressing the fusion and hemagglutinin-neuraminidase proteins. Journal of Veterinary Science. 2008; 9 (3): 301–308. https://doi.org/10.4142/jvs.2008.9.3.301

63. Luo S., Ren Y., Tarlavin N. V., Kraskov D. A., Javadov E. J., Xu D., et al. A DNA prime-inactivated boost regimen enhances immunogenicity against pigeon newcastle disease: a comparative study and analysis of synergistic effects. Veterinary Sciences. 2026; 13 (3):251. https://doi.org/10.3390/vetsci13030251

64. Razzaq S., Riaz A., Siddique N., Saif-Ur-Rehman, Shah M. A., Naeem K., Saleem G. Evaluation of genotype matched recombinant DNA vaccine for protection against genotype VII velogenic Newcastle disease virus in Pakistan. Scientific Reports. 2026; 16 (1):4402. https://doi.org/10.1038/s41598-025-34387-4


Supplementary files

1. Table. Characteristics of vaccines against duck virus hepatitis
Subject
Type Исследовательские инструменты
Download (521KB)    
Indexing metadata ▾

Review

For citations:


Bairashev T.A., Galeeva A.G., Efimova M.A. Improving immunoprophylaxis: potential and limitations of biotechnological solutions in Newcastle disease control. Veterinary Science Today. 2026;15(2):123-130. (In Russ.) https://doi.org/10.29326/2304-196X-2026-15-2-123-130

Views: 91

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)