COMPARATIVE PATHOLOGICAL STUDY OF EXPERIMENTAL INFECTION OF NEWCASTLE DISEASE VIRUS GENOTYPES VII IN CHICKENS AND DUCKS

Authors

  • Yassmin EL-Morshidy Department of Veterinary Pathology, Animal Health Research Institute(AHRI), Agriculture Research Center (ARC), Dokki, Giza, Egypt
  • Nagwan El-Habashi Department of Veterinary Pathology, Faculty of Veterinary Medicine, Kafrelsheikh University, 33516- Kafrelsheikh, Egypt
  • Ghada Abd EL–Dayem Department of poultry diseases, Animal Health Research Institute(AHRI), Agriculture Research Center (ARC), P.O. Box 246 Dokki, 12618 – Giza, Egypt
  • Ahmed El sawak Department of Veterinary Pathology, Faculty of Veterinary Medicine, Kafrelsheikh University, 33516- Kafrelsheikh, Egypt
  • Walied Abdo Department of Veterinary Pathology, Faculty of Veterinary Medicine, Kafrelsheikh University, 33516- Kafrelsheikh, Egypt

DOI:

https://doi.org/10.26873/SVR-1444-2021

Keywords:

Newcastle Disease, chicken, duck, virulent NDV-genotype VII challenge

Abstract

Newcastle disease virus (NDV) is a highly contagious virus infects a wide range of avian species including chicken and ducks. The disease can be fatal for many types of them. It was believed that ducks and geese act as natural reservoirs of NDV because of their natural resistance. Recently, NDV isolates were pathogenic for ducks. Therefore, our study aimed to investigate the pathogenicity of highly pathogenic NDV genotype VII in white Ross commercial broiler chickens and Mallard ducks on the basis of clinical, histological observation and immunohistochemistry findings of virus antigen through studying the sequential pathological lesions of both species at 2nd, 5th and 10th dpi. Both species were inoculated via intranasal route by NDV genotype VII (accession number MT887290). Clinical lesions and mortalities were evident mostly in chickens rather than in ducks. Respiratory, digestive and nervous signs were clearly manifested in chickens. Ducks showed low level of mortalities and the nervous signs were the most obvious symptoms. Microscopic findings of chickens showed severe pancreatitis, pneumonia, enteritis as well as pericarditis and brain malacia. Similar findings were noticed in ducks but with lower degree of severity. Brain lesions in ducks included encephalitis and perivascular reaction mostly within the cerebellar tissue. Immunohistochemistry reaction against NDV antigen showed marked immunostaining within epithelial cells, purkinje cells and inflammatory cells mostly the macrophages. The immunohistochemistry reaction was correlated with the pathological findings in both species. In conclusion, the mortality and lesions of NDV in both species were correlated with systemic alterations associated with pancreatitis, pneumonia and encephalopathy. Moreover, the obtained data revealed possible susceptibility of ducks to NDV genotype VII, which might be need forthcoming viral vaccination strategy for ducks against NDV.

References

● 1. Alexander, D., Newcastle disease and other paramyxovirus infections. Diseases of poultry, 1991.

● 2. Mayo, M., A summary of taxonomic changes recently approved by ICTV. Archives of virology, 2002. 147(8): p. 1655––6.

● 3. Mayo, M., Virus taxonomy-Houston 2002. Archives of virology, 2002. 147(5): p. 1071–6.

● 4. Kaleta, E.F. and C. Baldauf, Newcastle disease in free-living and pet birds, in Newcastle disease. 1988, Springer. p. 197–246.

● 5. Bulbule, N., et al., Virulence of Newcastle disease virus and diagnostic challenges. Adv. Anim. Vet. Sci, 2015. 3(5): p. 14–21.

● 6. Australia, A.H., Disease strategy, in Newcastle disease, N. disease, Editor. 2014: Australian Veterinary Emergency Plan (AUSVETPLAN).

● 7. Aziz-ul-Rahman, M.H. and M.Z. Shabbir, Suppl-2, M3: Adaptation of Newcastle Disease Virus (NDV) in Feral Birds and their Potential Role in Interspecies Transmission. The open virology journal, 2018. 12: p. 52.

● 8. Cappelle, J., et al., Empirical analysis suggests continuous and homogeneous circulation of Newcastle disease virus in a wide range of wild bird species in Africa. Epidemiology & Infection, 2015. 143(6): p. 1292–303.

● 9. Liu, H., et al., Characterization of Newcastle disease virus isolated from waterfowl in China. Avian diseases, 2008. 52(1): p. 150–5.

● 10. Elbestawy, A. R., Ellakany, H. F., Abd El-Hamid, H. S., Zedan, R. E., Gado, A. R., Sedeik, M. E., & Swelum, A. A. (2019). Muscovy ducks infected with velogenic Newcastle disease virus (genotype VIId) act as carriers to infect in-contact chickens. Poultry science, 98(10), 4441–8.

● 11. Wajid, A., et al., Complete genome sequence of a virulent Newcastle disease virus strain isolated from a clinically healthy duck (Anas platyrhynchos domesticus) in Pakistan. Genome announcements, 2016. 4(4): p. e00730–16.

● 12. Dai, Y., et al., Experimental infection of duck origin virulent Newcastle disease virus strain in ducks. BMC veterinary research, 2014. 10(1): p. 1–9.

● 13. Kang, Y., et al., Phylogenetic relationships and pathogenicity variation of two Newcastle disease viruses isolated from domestic ducks in Southern China. Virology journal, 2014. 11(1): p. 1–13.

● 14. Terregino, C. and I. Capua, Clinical traits and pathology of Newcastle disease infection and guidelines for farm visit and differential diagnosis, in Avian Influenza and Newcastle Disease. 2009, Springer. p. 113–22.

● 15. OIE, Office International des Epizooties, Manual of Standards for Diagnostic Tests and Vaccines. Newcastle Disease, 5th ed. Office International des Epizooties, Paris, 2004.

● 16. Bancroft, J.D. and M. Gamble, Theory and practice of histological techniques. 2008: Elsevier health sciences.

● 17. Anis, Z., et al., Comparative study on the pathogenesis of the generated 9a5b Newcastle disease virus mutant isolate between chickens and waterfowl. Veterinary pathology, 2013. 50(4): p. 638–47.

● 18. Samiullah, M., et al., Rising hyperimmune serum against avian paramyxovirus (APMV-1) and pigeon paramyxovirus (PPMV-1) in rabbits and their cross-reactivity. Pak. J. Biol. Sci, 2006. 9: p. 2184–6.

● 19. Carrasco, A.d.O.T., et al., Use of immunohis-tochemistry (IHC) in the detection of Newcastle disease virus (NDV) in experimentally and naturally infected birds. African Journal of Microbiology Research, 2015. 9(45): p. 2225–31.

● 20. Zenglei, H. and X. Liu, NDV induced immune-pathology in chickens. Hosts and Viruses, 2015. 2(2): p. 25.

● 21. Susta, L., et al., Pathologic characterization of genotypes XIV and XVII Newcastle disease viruses and efficacy of classical vaccination on specific pathogen-free birds. Veterinary pathology, 2015. 52(1): p. 120–31.

● 22. Abd El Aziz, M., El-Hamid, A., Ellkany, H., Nasef, S., Nasr, S., & El Bestawy, A. (2016). Biological and molecular characterization of Newcastle disease virus circulating in chicken flocks, Egypt, during 2014-2015. Zagazig Veterinary Journal, 44(1), 9–20.

● 23. Moharam, I., et al., Investigation of suspected Newcastle disease (ND) outbreaks in Egypt uncovers a high virus velogenic ND virus burden in small-scale holdings and the presence of multiple pathogens. Avian Pathology, 2019. 48(5): p. 406–15.

● 24. Abd El-Hamid, H. S., Shafi, M. E., Albaqami, N. M., Ellakany, H. F., Abdelaziz, N. M., Abdelaziz, M. N., & Elbestawy, A. R. (2020). Sequence analysis and pathogenicity of Avian Orthoavulavirus 1 strains isolated from poultry flocks during 2015–2019. BMC Veterinary Research, 16(1), 1–15.

● 25. Abd-Ellatieff, H. A., Abd El Aziem, A. N., Elbestawy, A. R., Goda, W. M., Belih, S. S., Ellakany, H. F., ... & El-Habashi, N. (2021). Efficacy of Vaccination against Infection with Velogenic Newcastle Disease Virus Genotypes VI and VII 1.1 Strains in Japanese Quails. Journal of Comparative Pathology, 186, 35–50.

● 26. Abd El Aziem, A., et al., Susceptibility of Japanese Quail and Chickens to Infection with Newcastle disease Virus Genotype VIId. Damanhour Journal of Veterinary Sciences, 2020. 3(2): p. 27–31.

● 27. Schilling, M.A., et al., Innate immune genes associated with newcastle disease virus load in chick embryos from inbred and outbred lines. Frontiers in microbiology, 2019. 10: p. 1432.

● 28. Kabiraj, C.K., et al., Sequential pathology of a genotype XIII Newcastle disease virus from Bangladesh in chickens on experimental infection. Pathogens, 2020. 9(7): p. 539.

● 29. Pandarangga, P., et al., Pathogenesis of new strains of Newcastle disease virus from Israel and Pakistan. Veterinary pathology, 2016. 53(4): p. 792–6.

● 30. Susta, L., et al., Clinicopathological characteriza-tion in poultry of three strains of Newcastle disease virus isolated from recent outbreaks. Veterinary pathology, 2011. 48(2): p. 349–60.

● 31. Miller, P.J. and G. Koch, Newcastle disease. Diseases of poultry, 2013. 13: p. 89–138.

● 32. Rasoli, M., et al., Alteration in lymphocyte responses, cytokine and chemokine profiles in chickens infected with genotype VII and VIII velogenic Newcastle disease virus. Comparative Immunology, Microbiology and Infectious Diseases, 2014. 37(1): p. 11–21.

● 33. Okpe, G.C., et al., Vitamin A dietary supplementation reduces the mortality of velogenic Newcastle disease significantly in cockerels. International journal of experimental pathology, 2015. 96(5): p. 326–31.

● 34. Etriwati, D.R., E. Handharyani, and S. Setiyaningsih, Pathology and immunohistochemistry study of Newcastle disease field case in chicken in Indonesia. Veterinary world, 2017. 10(9): p. 1066.

● 35. Ezema, W.S., et al., Atrophy of the lymphoid organs and suppression of antibody response caused by velogenic Newcastle disease virus infection in chickens. Tropical animal health and production, 2016. 48(8): p. 1703–9.

● 36. Friend, M. and D. Trainer, Experimental Newcastle disease studies in the mallard. Avian diseases, 1972: p. 700–13.

● 37. Abdo, W., et al., Pathological and immuno-histochemical findings of natural highly pathogenic avian influenza infection in tufted ducks during 2010–2011 outbreaks in Japan. Journal of Veterinary Medical Science, 2014. 76(9): p. 1285–90.

● 38. Aldous, E., et al., Infection dynamics of highly pathogenic avian influenza and virulent avian paramyxovirus type 1 viruses in chickens, turkeys and ducks. Avian Pathology, 2010. 39(4): p. 265–73.

● 39. Ezema, W., J. Okoye, and J. Nwanta, LaSota vaccination may not protect against the lesions of velogenic Newcastle disease in chickens. Tropical animal health and production, 2009. 41(4): p. 477–84.

● 40. Manzoor, A.W., et al., Pathotyping of Newcastle disease virus using multiplex reverse transcription polymerase chain reaction and pathological studies in naturally infected broiler chicks. Pak. J. Life Soc. Sci, 2013. 11: p. 225–32.

● 41. Wang, Y., et al., Lack of detection of host associated differences in Newcastle disease viruses of genotype VIId isolated from chickens and geese. Virology Journal, 2012. 9(1): p. 1–15.

● 42. Ecco, R., et al., Neurological lesions in chickens experimentally infected with virulent Newcastle disease virus isolates. Avian pathology, 2011. 40(2): p. 145–52

● 43. Bergfeld, J., et al., An Australian Newcastle disease virus with a virulent fusion protein cleavage site produces minimal pathogenicity in chickens. Veterinary pathology, 2017. 54(4): p. 649–60.

● 44. Brar, R., et al., Diagnosis of Newcastle disease in broiler by histopathology and immunohistochemistyr. 2017. P. 60–62

● 45. Asplin, F., Newcastle disease in ducks and geese. The Veterinary Record, 1947. 59(45): p. 621–4.

● 46. Bouzari, M. The response of ducks to V4 Newcastle disease virus and its transmission to contact ducks and domestic chickens. in Veterinary research forum: an international quarterly journal. 2014. Faculty of Veterinary Medicine, Urmia University, Urmia, Iran.

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Published

2021-12-17

How to Cite

EL-Morshidy, Y., El-Habashi, N., Abd EL–Dayem, G., El sawak, A., & Abdo, W. (2021). COMPARATIVE PATHOLOGICAL STUDY OF EXPERIMENTAL INFECTION OF NEWCASTLE DISEASE VIRUS GENOTYPES VII IN CHICKENS AND DUCKS. Slovenian Veterinary Research, 58(24-Suppl), 243–58. https://doi.org/10.26873/SVR-1444-2021

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Original Research Article