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Contribution of some immunological and metabolic factors to formation of piglets’ post-vaccination immunity

https://doi.org/10.21323/2414-438X-2022-7-3-193-199

Abstract

The role and responsibility of natural resistance factors, protein and lipid metabolism in the formation of piglets post-vaccination immunity against circovirus is researched. Blood was taken for tests before and on the 15th, 40th and 70th day after the vaccination. The sampled blood was analyzed to determine immunological and biochemical parameters. It was revealed that before vaccination, 31.46% of the studied samples have a positive reaction in ELISA; their number increases to 67.80–71.16% on the 40th and 70th days after vaccination.In the blood of piglets, especially on the 40th and 70th day after the vaccination, the total count of leukocytes, monocytes and lymphocytes increases by 1.21; 2.28 times and 1.48 times, but neutrophils reduced by 1.74 times along with the phagocytic properties activation. The anabolic directivity of protein metabolism is defined by the synthesis of globulin proteins. At the same time albumin-synthesizing activity in a liver decreased and “cytolysis reaction” of hepatocytes was detected. In the lipid profile of piglets’ blood, the content of LDL‑cholesterol increased by 1.44 times, while that of triglycerides decreased by 2.64 times. X‑ray spectral analysis revealed the correlation between the formation of post-vaccination immunity and two factors: the factor of the principal component (PC) 1, which is predominantly associated with indicators of natural resistance, and PC2, which is associated with metabolism indicators. The research results show that in order to increase the efficiency of formation of post-vaccination immunity in piglets, it is necessary to combine vaccination with hepatoprotective drugs.

About the Authors

M. A. Derkho
South Ural State Agrarian University
Russian Federation

Marina A. Derkho, Doctor of Biological Sciences, Professor, Institute of Veterinary Medicine

13, Gagarin str., Troitsk, 457103

Tel.: +7–351–632–00–10



P. V. Burkov
South Ural State Agrarian University
Russian Federation

Pavel V. Burkov, Candidate of Veterinary Sciences, Docent, Institute of Veterinary Medicine

3, Gagarin str., Troitsk, 457103

Tel.: +7–351–632–00–10



P. N. Shcherbakov
South Ural State Agrarian University
Russian Federation

Pavel N. Shcherbakov, Doctor of Veterinary Sciences, Docent, Institute of Veterinary Medicine

3, Gagarin str., Troitsk, 457103

Tel.: +7–351–632–00–10



M. B. Rebezov
V.M. Gorbatov Federal Scientific Center of Food Systems
Russian Federation

Maksim B. Rebezov, Doctor of Agricultural Sciences, Candidate of Veterinary Sciences, Professor, Leading Researcher

26, Talalikhin str., 109316, Moscow

Tel.: +7–999–900–23–65



K. V. Stepanova
South Ural State Agrarian University
Russian Federation

Ksenia V. Stepanova, Candidate of Biological Sciences, Docent, Institute of Veterinary Medicine

13, Gagarin str., Troitsk, 457103

Tel.: +7–351–632–00–10



A. N. M. Ansori
Universitas Airlangga
Indonesia

Arif N. M. Ansori, Doctor in Veterinary Science, Faculty of Veterinary Medicine

Jl. Mulyorejo, Kec. Mulyorejo, Surabaya, East Java, 60115



References

1. Yirga, A., Jemberu, W.T., Lyons, N., Gebru, A., Akililu, F., Rushton, J. (2020). Post-vaccination herd immunity against peste des petits ruminants and inter-vaccination population turnover in small ruminant flocks in northwest Ethiopia. Preventive Veterinary Medicin, 174, Article 104850. https://doi.org/10.1016/j.prevetmed.2019.104850

2. Li, C., Culhane, M.R., Cheeran, M., Galina Pantoja, L., Jansen, M., Amodie, D. et al. (2020). Exploring heterologous prime-boost vaccination approaches to enhance influenza control in pigs. Veterinary Research, 51(1), Article 89. https://doi.org/10.1186/s13567–020–00810-z

3. Yang, S., Park, S. -J., Oh, T., Cho, H., Chae, C. (2020). Efficacy comparison of commercial porcine circovirus type 2 (Pcv2) and mycoplasma hyopneumoniae monovalent and bivalent vaccines against a dual challenge. Canadian Journal of Veterinary Research, 84(4), 272–282.

4. Oh, T., Park, K.H., Yang, S., Jeong, J., Kang, I., Park, C. et al. (2019). Evaluation of the efficacy of a trivalent vaccine mixture against a triple challenge with Mycoplasma hyopneumoniae, PCV2, and PRRSV and the efficacy comparison of the respective monovalent vaccines against a single challenge. BMC Veterinary Research, 15(1), Article 342. https://doi.org/10.1186/s12917–019–2091–6

5. Karuppannan, A.K., Opriessnig, T. (2017). Porcine circovirus Type 2 (PCV2) vaccines in the context of current molecular epidemiology. Viruses, 9(5), Article 99. https://doi.org/10.3390/v9050099

6. Alarcon, P, Rushton, J, Wieland, B. (2013). Cost of postweaning multi-systemic wasting syndrome and porcine circovirus type‑2 subclinical infection in England — an economic disease model. Preventive Veterinary Medicine, 110(2), 88–102. https://doi.org/10.1016/j.prevetmed.2013.02.010

7. Feng, H., Segalés, J., Wang, F., Jin, Q., Wang, A., Zhang, G. et al. (2022). Comprehensive analysis of codon usage patterns in Chinese porcine circoviruses based on their major protein-coding sequences. Viruses, 14(1), Article 81. https://doi.org/10.3390/v14010081

8. Burkov, P.V., Shcherbakov, P.N., Derkho, M.A., Rebezov, M.B. (2022). Peculiarities of post-vaccination immunity formation against porcine circovirus infection and its correction. Agrarian Science, 363(10), 30–36. https://doi.org/10.32634/0869–8155–2022–363–10–30–36 (In Russian)

9. Raev, S., Yuzhakov, A., Aliper, T. (2021). Whole-genome analysis of porcine circovirus type 2 in Russia. Pathogens, 10(12), Article 1631. https://doi.org/10.3390/pathogens10121631

10. Opriessnig, T., Gomes-Neto, J.C., Hemann, M., Shen, H.-G., Beach, N. M., Huang, Y. et al. (2011). An experimental live chimeric porcine circovirus 1–2a vaccine decreases porcine circovirus 2b viremia when administered intramuscularly or orally in a porcine circovirus 2b and porcine reproductive and respiratory syndrome virus dual-challenge model. Microbiology and Immunology, 55(12), 863–873. https://doi.org/10.1111/j.1348–0421.2011.00385.x

11. Lee, S.-I., Jeong, C.-G., ul Salam Mattoo, S., Nazki, S., Prasad Aganja, R., Kim, S.-C. (2021). Protective immunity induced by concurrent intradermal injection of porcine circovirus type 2 and Mycoplasma hyopneumoniae inactivated vaccines in pigs. Vaccine, 39(45), 6691–6699. https://doi.org/10.1016/j.vaccine.2021.07.043

12. Temple, D., Jiménez, M., Escribano, D., Martín-Valls, G., Díaz, I., Manteca, X. (2020). Welfare benefits of intradermal vaccination of piglets. Animals, 10(10), Article 1898. https://doi.org/10.3390/ani10101898

13. Niu, X., Ding, Y., Chen, S., Gooneratne, R., Ju, X. (2022). Effect of immune stress on growth performance and immune functions of livestock: Mechanisms and prevention. Animals, 12(7), Article 909. https://doi.org/10.3390/ani12070909

14. Sun, Y.I., Pence, B.D., Wang, S.S., Woods, J.A. (2019). Effects of exercise on stress-induced attenuation of vaccination responses in mice. Medicine and Science in Sports and Exercise, 51(8), 1635–1641. https://doi.org/10.1249/MSS.0000000000001971

15. Li, X., Liu, S., Wang, J., Yi, J., Yuan, Z., Wu, J. et al. (2021). Effects of ND vaccination combined LPS on growth performance, antioxidant performance and lipid metabolism of broiler. Research in Veterinary Science, 135, 317–323. https://doi.org/10.1016/j.rvsc.2020.10.007

16. Janmohammadi, A., Sheikhi, N., Nazarpak, H.H., Brujeni, G.N. (2020). Effects of vaccination on acute-phase protein response in broiler chicken. PLoS One, 15(2), Article e0229009. https://doi.org/10.1371/journal.pone.0229009

17. Hernández-Caravaca, I., Gourgues, S.F., Rodríguez, V., Estrada, E. D., Cerón, J.J., Escribano, D. (2017). Serum acute phase response induced by different vaccination protocols against circovirus type 2 and Mycoplasma hyopneumoniae in piglets. Research in Veterinary Science, 114, 69–73. https://doi.org/10.1016/j.rvsc.2017.03.006

18. Jeong, J., Kang, I., Kim, S., Park, K. H., Park, C., Chae, C. (2018). Comparison of 3 vaccination strategies against porcine reproductive and respiratory syndrome virus, Mycoplasma hyopneumoniae, and porcine circovirus type 2 on a 3 pathogen challenge model. Canadian Journal of Veterinary Research, 82(1), Article 9, 39–47.

19. Derkho, M.A., Baltabekova, A. Zh., Balabaev, B.K., Derkho, A.O. (2021). Biochemical blood profile of the Kazakh white-headed breed depending on age. International Transaction Journal of Engineering, Management, & Applied Sciences & Technologies, 12(12), Article 12A12K, 1–11. http://doi.org/10.14456/ITJEMAST.2021.242

20. Derkho, M.A., Balabaev, B.K., Baltabekova, A. Zh., Sereda, T.I., Eliseenkova, M.V. (2022). Assessment of the influence of age and lactation period on the variability of blood biochemical composition of Kazakh whitehead cows. International Transaction Journal of Engineering, Management, & Applied Sciences & Technologies, 13(3), Article 13A3F, 1–12. https://doi.org/10.14456/ITJEMAST.2022.48

21. Vincent, A., Awada, L., Brown, I., Chen, H., Claes, F., Dauphin, G. et al. (2014). Review of influenza A virus in swine worldwide: A call for increased surveillance and research. Zoonoses and Public Health, 61(1), 4–17. https://doi.org/10.1111/zph.12049

22. Jackson, D.A. (1993). Stopping rules in principal component analysis: a comparison of heuristical and statistical approaches. Ecology, 74(8), 2204–2214. https://doi.org/10.2307/1939574

23. Hammer, Ø., Harper, D.A.T., Ryan, P.D. (2001). Past: Paleontological Statistics Software Package for Education and Data Analysis. Palaeontologia Electronica, 4(1), Article 4, 1–9.

24. Martelli, P., Saleri, R., Ferrarini, G., De Angelis, E., Cavalli, V., Benetti, M. et al. (2016). Impact of maternally derived immunity on piglets’ immune response and protection against porcine circovirus type 2 (PCV2) after vaccination against PCV2 at different age. BMC Veterinary Research, 12(1), Article 77. https://doi.org/10.1186/s12917–016–0700–1

25. Sorokina, S.A., Derkho, M.A., Gizatullina, F.G., Sereda T. I. (2022). Leukocytes as indicators of the accumulation of metals in the body of growing chicks. International Transaction Journal of Engineering, Management, & Applied Sciences & Technologies,13(4), Article 13A4R, 1–11. https://doi.org/10.14456/ITJEMAST.2022.82

26. Yanich, T.V., Derkho, M.A., Tegza, A. (2022). Hemostatic profile of holstein heifers depending on age. International Transaction Journal of Engineering, Management, & Applied Sciences & Technologies, 13(1), Article 13A1U, 1–11. https://doi.org/10.14456/ITJEMAST.2022.21

27. Opriessnig, T., Castro, A.M.M.G., Karuppanan, A.K., Gauger, P. C., Halbur, P. G., Matzinger, S.R. et al. (2019). A porcine circovirus type 2b (PCV2b)-based experimental vaccine is effective in the PCV2b-Mycoplasma hyopneumoniae coinfection pig model. Vaccine, 37(44), 6688–6695. https://doi.org/10.1016/j.vaccine.2019.09.029

28. Tassis, P.D., Tsakmakidis, I., Papatsiros, V.G., Koulialis, D., Nell, T., Brellou, G. et al. (2017). A randomized controlled study on the efficacy of a novel combination vaccine against enzootic pneumonia (Mycoplasma hyopneumoniae) and porcine Circovirus type 2 (PCV2) in the presence of strong maternally derived PCV2 immunity in pigs. BMC Veterinary Research, 13(1), Article 91. https://doi.org/10.1186/s12917–017–1014–7

29. Rakibuzzaman, A., Piñeyro, P., Pillatzki, A., Ramamoorthy, S. (2021). Harnessing the genetic plasticity of porcine circovirus type 2 to target suicidal replication. Viruses, 13(9), Article1676. https://doi.org/10.3390/v13091676

30. Pooley, H.B., Begg, D.J., Plain, K.M., Whittington, R.J., Purdie, A.C., De Silva, K. (2019). The humoral immune response is essential for successful vaccine protection against paratuberculosis in sheep. BMC Veterinary Research, 15(1), Article 223. https://doi.org/10.1186/s12917–019–1972-z

31. Li, F., Wang, X., Ma, R., Wu, W., Teng, F., Cheng, X. et al. (2021). Oral immunization with lactobacillus casei expressing the porcine circovirus type 2 cap and LTB induces mucosal and xystemic antibody responses in mice. Viruses, 13(7), Article 1302. https://doi.org/10.3390/v13071302

32. Sobolev, O., Binda, E., O’Farrell, S., Lorenc, A., Pradines, J., Huang, Y. et al. (2016). Adjuvanted influenza-H1N1 vaccination reveals lymphoid signatures of age-dependent early responses and of clinical adverse events. Nature Immunology, 17(2), 204–213. https://doi.org/10.1038/ni.3328

33. Efe, C., Harputluoğlu, M., Soylu, N.K., Yilmaz, S. (2022). Letter to the editor: Liver transplantation following severe acute respiratory syndrome-coronavirus‑2 vaccination-induced liver failure. Hepatology, 75(6), 1669–1671. https://doi.org/10.1002/hep.32409

34. Jiang, H., Wang, D., Wang, J., Zhu, S., She, R., Ren, X. et al. (2019). Induction of porcine dermatitis and nephropathy syndrome in piglets by infection with porcine circovirus type 3. Journal of Virology, 93(4), Article e02045–18. https://doi.org/10.1128/JVI.02045–18

35. Prajapati, K.D., Sharma, S.S., Roy, N. (2011). Current perspectives on potential role of albumin in neuroprotection. Reviews in the Neurosciences, 22(3), 355–363. https://doi.org/10.1515/RNS.2011.028

36. Autschbach, F., Meuer, S.C., Moebius, U., Manns, M., Hess, G., Zum Büschenfelde, K.‐H. M. et al. (1991). Hepatocellular expression of lymphocyte function-associated antigen 3 in chronic hepatitis. Hepatology, 14(2), 223–30.

37. Sirisereewan, C., Thanawongnuwech, R., Kedkovid, R. (2022). Current understanding of the pathogenesis of porcine circovirus 3. Pathogens, 11(1), Article 64. https://doi.org/10.3390/pathogens11010064

38. Fukami, H., Morinaga, J., Nakagami, H., Hayashi, H., Okadome, Y., Matsunaga, E. et al. (2021). Vaccine targeting ANGPTL3 ameliorates dyslipidemia and associated diseases in mouse models of obese dyslipidemia and familial hypercholesterolemia. Cell Reports Medicine, 2(11), Article 100446. https://doi.org/10.1016/j.xcrm.2021.100446

39. Vania, L., Widyananda, М.Н., Kharisma, V.D., Muhammad Ansori, A.N., Naw, S.W., Maksimiuk, N. et al. (2021). Anticancer activity prediction of Garcinia mangostana L. against HER2-positive breast cancer through inhibiting EGFR, HER2 and IGF1R protein: A bioinformatics study. Biochemical and Cellular Archives, 21(2), 3313–3321.


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For citations:


Derkho M.A., Burkov P.V., Shcherbakov P.N., Rebezov M.B., Stepanova K.V., Ansori A.M. Contribution of some immunological and metabolic factors to formation of piglets’ post-vaccination immunity. Theory and practice of meat processing. 2022;7(3):193-199. https://doi.org/10.21323/2414-438X-2022-7-3-193-199

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