Abstract
Newcastle disease (ND), caused by virulent Avian avulavirus 1 (AAvV 1), affects variety of avian species around the globe. Several AAvV 1 viruses of different genotypes have recently emerged with varying clinical impacts on their susceptible hosts. Although experimental infection with velogenic and mesogenic strains in chickens and pigeons is well-studied, nevertheless, there exists a paucity of data for comparative variations in serum biochemistry profile of susceptible hosts upon challenge with isolates of varying pathogenicities. With this background, a comparative assessment of a range of serum biochemical parameters was made following challenge with duck-originated velogenic strain (sub-genotype VIIi; MF437287) and pigeon-originated mesogenic strain (sub-genotype VIm; KU885949) in chickens and pigeons. For each of the isolate, commercial broiler chickens and wild pigeons were challenged (10–6.51 EID50/0.1 mL for sub-genotype VIIi and 10–6.87 EID50/0.1 mL sub-genotype Vim) separately via intranasal and intraocular route. Sera were collected on 0, 3rd, 5th, 7th, and 9th day post-infection (dpi), and processed for quantitative analysis of different biochemical parameters. By day 3 post-infection (pi), a substantial decrease (p < 0.0001) in serum alkaline phosphatase (ALP) was observed in chickens and pigeons challenged with velogenic isolate. On the other hand, from day 5 pi and onward, a significant increase (p < 0.001) in serum ALP and total protein concentration was observed exclusively in pigeons challenged with mesogenic isolate. For serum aspartate aminotransferase (AST), a significant increase (p < 0.05) in concentration was observed on day 3 pi which decreased from day 5 pi and onward in pigeons and chickens challenged with mesogenic isolate. Also, to reveal antigenic differences among homologous and heterologous vaccine and field-prevalent strains, cross-hemagglutination inhibition assay demonstrated antigenically diverse nature (R-value < 0.5) of both strains from vaccine strain (LaSota, genotype II). The study concludes antigenic differences among prevalent genotypes than vaccine strain and, although requires further studies to ascertain study outcomes, the serum biochemical profile may facilitate presumptive diagnosis of disease in their susceptible hosts.
Similar content being viewed by others
References
Akhtar, S., Muneer, M.A., Muhammad, K., Tipu, M.Y., Rabbani, M., Shabbir, M.Z., 2016. Genetic characterization and phylogeny of pigeon paramyxovirus isolate (PPMV-1) from Pakistan. Springerplus, 5(1), 1295.
Al-Hussary, N.A., Kudair, I.M., 2010. Effect of vaccination on some biochemical parameters in broiler chickens. Iraqi Journal of Veterinary Sciences, 24(2), 59–64.
Archetti, I., Horsfall, F.L., 1950. Persistent antigenic variation of influenza A viruses after incomplete neutralization in ova with heterologous immune serum. Journal of Experimental Medicine, 92, 441–462.
Aricibasi, M., Jung, A., Heller, E.D., Rautenschlein, S., 2010. Differences in genetic background influence the induction of innate and acquired immune responses in chickens depending on the virulence of the infecting infectious bursal disease virus (IBDV) strain. Veterinary Immunology and Immunopathology, 135(1–2), 79–92.
Aziz-ul-Rahman, Rohaim, M.A., El Naggar, R.F., Mustafa, G., Chaudhry, U., Shabbir, M.Z., 2019. Comparative clinico-pathological assessment of velogenic (sub-genotype VIIi) and mesogenic (sub-genotype VIm) Avian avulavirus 1 in chickens and pigeons. Avian Pathology, 48(6), 610–621.
Aziz-ul-Rahman, Yaqub, T., Imran, M., Habib, M., Sohail, T., Furqan, S.M., Munir, M., Shabbir, M.Z., 2018. Phylogenomics and infectious potential of Avian Avulaviruses species-type 1 isolated from healthy green-winged teal (Anas carolinensis) from a wetland sanctuary of Indus river. Avian Diseases, 62(4), 404–15.
Dimitrov, K.M., Ferreira, H.L., Pantin-Jackwood, M.J., Taylor, T.L., Goraichuk, I.V., Crossley, B.M., Killian, M.L., Bergeson, N.H., Torchetti, M.K., Afonso, C.L., Suarez, D.L., 2019. Pathogenicity and transmission of virulent Newcastle disease virus from the 2018–2019 California outbreak and related viruses in young and adult chickens. Virology, 531, 203–18.
Dortmans, J.C., Peeters, B.P., Koch, G., 2012. Newcastle disease virus outbreaks: vaccine mismatch or inadequate application?. Veterinary Microbiology, 160(1–2), 17–22.
Enam, S.J., Oladele, S.B., James, A.A., Balami, A.G., Idris, S.Y., Abdu, P.A., 2018. Serum biochemical values of some species of apparently healthy free-living wild birds in Zaria, Nigeria. Comparative Clinical Pathology, 27(2), 477–81.
Ezema, W.S., Eze, D.C., Shoyinka, S.V.O., Okoye, J.O.A., 2016. Atrophy of the lymphoid organs and suppression of antibody response caused by velogenic Newcastle disease virus infection in chickens. Tropical Animal Health and Production, 48(8), 1703–1709.
Faeji, C.O., Oladunmoye, M.K., Adebayo, I.A., Adebolu, T.T., 2019. Haematological and Gross Pathological Changes in Broilers Experimentally Challenged with Velogenic Strain of Newcastle Disease Virus. Asian Hematology Research Journal, 27, 1–5.
Gogoi, P., Ganar, K., Kumar, S., 2017. Avian paramyxovirus: a brief review. Transboundary and emerging diseases, 64(1), 53–67.
Guo, H., Liu, X., Xu, Y., Han, Z., Shao, Y., Kong, X., Liu, S., 2014. A comparative study of pigeons and chickens experimentally infected with PPMV-1 to determine antigenic relationships between PPMV-1 and NDV strains. Veterinary Microbiology, 168, 88–97.
Hu, S., Ma, H., Wu, Y., Liu, W., Wang, X., Liu, Y., Liu, X., 2009. A vaccine candidate of attenuated genotype VII Newcastle disease virus generated by reverse genetics. Vaccine, 27(6), 904–10.
Igwe, A.O., Afonso, C.L., Ezema, W.S., Brown, C.C., Okoye, J.O., 2018. Pathology and distribution of velogenic viscerotropic Newcastle disease virus in the reproductive system of vaccinated and unvaccinated laying hens (Gallus gallus domesticus) by immunohistochemical labelling. Journal of comparative pathology, 159, 36–48.
Kim, L.M., King, D.J., Guzman, H., Tesh, R.B., da Rosa, A.P.T., Bueno, R., Dennett, J.A., Afonso, C.L., 2008. Biological and phylogenetic characterization of pigeon paramyxovirus serotype 1 circulating in wild North American pigeons and doves. Journal of Clinical Microbiology, 46, 3303–3310.
Kommers, G.D., King, D.J., Seal, B.C., Brown, C.C., 2001. Virulence of pigeon-origin Newcastle disease virus isolates for domestic chickens. Avian Diseases, 45(4), 906–921.
Malik, M., Sohail, M., Sajid, H., Hamidullah, S., Bano, N., Shah, S., 2018. Effects of Newcastle disease virus on different haematological parameters in broilers. Advance in Animal Veterinary Sciences, 6(4), 183–6.
Matanović, K., Severin, K., Martinković, F., Šimpraga, M., Janicki, Z., Barišić, J., 2007. Hematological and biochemical changes in organically farmed sheep naturally infected with Fasciola hepatica. Parasitology Research, 101(6), 1657–61.
Miller, P.J., King, D.J., Afonso, C.L., Suarez, D.L., 2007. Antigenic differences among Newcastle disease virus strains of different genotypes used in vaccine formulation affect viral shedding after a virulent challenge. Vaccine, 25(41), 7238–46.
Munir, M., Cortey, M., Abbas, M., Afzal, F., Shabbir, M.Z., Khan, M.T., Ahmed, S., Ahmad, S., Baule, C., Ståhl, K., Zohari, S., 2012. Biological characterization and phylogenetic analysis of a novel genetic group of Newcastle disease virus isolated from outbreaks in commercial poultry and from backyard poultry flocks in Pakistan. Infection, Genetics and Evolution, 12(5), 1010–1019.
Njagi, L.W., Mbuthia, P.G., Nyaga, P.N., Bebora, L.C., Minga, U.M., 2012. Viral nucleoprotein localization and lesions of Newcastle disease in tissues of indigenous ducks. Tropical Animal Health and Production, 44(4), 747–750
Okorie-Kanu, C.O., Okorie-Kanu, O.J., Okoye, J.O., 2016. Blood biochemistry responses of chickens experimentally infected with a velogenic Newcastle disease virus (Kudu 113). Nigerian Veterinary Journal, 37(3), 160–74.
Okoroafor, O.N., Okorie-Kanu, C.O., Animoke, P.C., Okoye, J.A., Nwanta, J.A., Anene, B.M., 2018. Comparison of blood biochemistry responses of cockerels and turkeys experimentally infected with a velogenic newcastle disease virus. Nigerian Veterinary Journal, 39(2), 168–80.
Panshin, A., Shihmanter, E., Weisman, Y., Örvell, C., Lipkind, M., 2002. Antigenic heterogeneity among the field isolates of Newcastle disease virus (NDV) in relation to the vaccine strain: 1. Studies on viruses isolated from wild birds in Israel. Comparative Immunology, Microbiology and Infectious Diseases, 25, 95–108.
Ren, S., Wang, C., Zhang, X., Zhao, L., Wang, X., Yao, W., Han, Q., Wang, Y., Fan, M., Gao, X., Xiao, S., 2017. Phylogenetic and pathogenic characterization of a pigeon paramyxovirus type 1 isolate reveals cross-species transmission and potential outbreak risks in the northwest region of China. Archives of Virology, 162, 2755–2767.
Rivetz, B., Bogin, E., Hornstein, K., Merdinger, M., 1975. Biochemical changes in chicken serum during infection with strains of Newcastle disease virus of differing virulence. I. Enzyme study. Avian Pathology, 4(3), 189–97.
Samour, J., 2014. Newcastle disease in captive falcons in the Middle East: a review of the clinical and pathologic findings. Journal of Avian Medicine and Surgery, 28(1), 1–5.
Shabbir, M.Z., Akhtar, S., Tang, Y., Yaqub, T., Ahmad, A., Mustafa, G., Alam, M.A., Santhakumar, D., Nair, V., 2016. Infectivity of wild bird origin avian Paramyxovirus serotype 1 and vaccine effectiveness in chickens. Journal of General Virology, 97, 3161–3173.
Southwood, L.L., Frisbie, D.D., Kawcak, C.E., McIlwraith, C.W., 2003. Evaluation of serum biochemical markers of bone metabolism for early diagnosis of nonunion and infected nonunion fractures in rabbits. American Journal of Veterinary Research, 64(6), 727–35.
Sugiharto, S., Yudiarti, T., Isroli, I., Widiastuti, E., Wahyuni, H.I., Sartono, T.A., 2018. Intestinal microbial ecology and serum biochemistry of avian pathogenic Escherichia coli infected broilers fed multistrain probiotic preparation. Livestock Research for Rural Development, 30(8).
Susta, L., Segovia, D., Olivier, T.L., Dimitrov, K.M., Shittu, I., Marcano, V., Miller, P.J., 2018. Newcastle Disease Virus Infection in Quail. Veterinary Pathology, 55(5), 682–92.
Talebi, A., 2006. Biochemical parameters in broiler chickens vaccinated against ND, IB and IBD. International Journal of Poultry Science, 5: 1151–1155.
Ugochukwu, I.C., Ugochukwu, E.I., Chukwu, C.C., 2018. Haematological parameters and serum biochemical assay of West African dwarf goats infected with peste des petits ruminants virus in Nsukka, Enugu State. Comparative Clinical Pathology, 27(1), 13–9.
Wakamatsu, N., King, D.J., Kapczynski, D.R., Seal, B.S., Brown, C.C., 2006. Experimental pathogenesis for chickens, turkeys, and pigeons of exotic Newcastle disease virus from an outbreak in California during 2002-2003. Veterinary Pathology, 43(6), 925–933.
Xiao, S., Nayak, B., Samuel, A., Paldurai, A., Kanabagattebasavarajappa, M., Prajitno, T.Y., Bharoto, E.E., Collins, P.L., Samal, S.K., 2012. Generation by reverse genetics of an effective, stable, live-attenuated Newcastle disease virus vaccine based on a currently circulating, highly virulent Indonesian strain. PloS one, 7(12), e52751.
Xue, C., Xu, X., Yin, R., Qian, J., Sun, Y., Wang, C., Ding, C., Yu, S., Hu, S., Liu, X., Cong, Y., 2017. Identification and pathotypical analysis of a novel VIk sub-genotype Newcastle disease virus obtained from pigeon in China. Virus Research, 238, 1–7.
Zahid, B., Aslam, A., Chaudhry, Z.I., Akhtar, R., 2017. Biochemical and histopathological changes in immune and non-immune broilers after inoculation of field infectious bursal disease virus. Pakistan Journal of Zoology, 49(4), 1279–1283.
Zhang, J., Kaiser, M.G., Deist, M.S., Gallardo, R.A., Bunn, D.A., Kelly, T.R., Dekkers, J.C., Zhou, H., Lamont, S.J., 2018. Transcriptome analysis in spleen reveals differential regulation of response to Newcastle disease virus in two chicken lines. Scientific Reports, 8(1), 1278.
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
The current study was carried out following the Guide for the Care and Use of Laboratory Animals by National Institutes of Health and Animal Research Council (https://grants.nih.gov/grants/olaw/guide-for-the-care-and-use-of-laboratory-animals.pdf). All protocols including bird’s management, virus challenge procedure, serum sampling, and bird’s sacrificial procedure were approved by the Ethical Review Committee for Use of Laboratory Animals (ERCULA) of University of Veterinary and Animal Sciences, Lahore (Permit Number: ORIC/DR-70).
Conflict of interest
The authors declare that they have no conflict of interests.
Additional information
Publisher’s note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
About this article
Cite this article
Ul-Rahman, A., Shabbir, M.A.B., Ahmed, M. et al. A comparative evaluation of serum biochemistry profile and antigenic relatedness among velogenic and mesogenic Avian avulavirus 1 infection in chickens and pigeons. Trop Anim Health Prod 52, 1977–1984 (2020). https://doi.org/10.1007/s11250-020-02215-8
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s11250-020-02215-8