ANTIBACTERIAL ACTIVITY OF PHAGOCYTOSIS OF DOMESTIC DUCK ERYTHROCYTES

Keywords: duck, erythrocyte, microscope, bacterium, adhesion, blood, phagocytosis

Abstract

It is known that in the lumen of blood vessels there is a large number of blood-forming elements, namely erythrocytes, which make up approximately 95% of the total number of blood cells. Erythrocytes are red blood cells or known as red blood cells. They are motile, differentiated blood cells in most vertebrates and some invertebrates. It is known that erythrocytes lose their cytoplasmic organelles and nucleus in the process of development. As a result, they adapted to perform actually only one function, actually respiratory. It is performed due to the presence in them of a breathing pigment called hemoglobin. That is, it is known that erythrocytes are anucleated red blood cells whose function is to transport oxygen. Although we already know that the main function of erythrocytes is to transport oxygen to vital organs, recent studies have shown that mammalian erythrocytes also participate in the immune response to bacterial infections in animals. However, the immune mechanisms used by bird erythrocytes are still not fully understood. Therefore, we demonstrated that erythrocytes of domestic ducks (Anas platyrhynchos domesticus) have the ability to phagocytosis and also exhibit antibacterial activity. Phagocytosis (from the Greek means "devourer") performs the function of active capture and absorption of such objects as cell fragments, bacteria and other solid particles by unicellular organisms. First, the phagocytic and adhesive activity of bird erythrocytes was determined using a scanning electron raster microscope. Adhesion, as we know, comes from Latin - adhesion or adhesion of various liquid or solid forms. With the help of low results, it was proved that duck erythrocytes had a wide range of phagocytic and adhesive activity when contaminated with various bacteria. The statistical data were then further investigated and established that duck erythrocytes contain the ability to produce reactive oxygen species (ROS) and inducible nitric oxide synthase (iNOS) in response to bacterial stimulation. And as a result, it was also found that the bird's erythrocytes had a fairly powerful antibacterial activity against all three bacteria, while the stimulation of the two types of bacteria significantly increased the expression of inflammatory factors and increased the production of antioxidant enzymes to protect cells from oxidative damage.

References

1. Balcerczyk, A., Soszynski, M., Rybaczek, D., Przygodzki, T., Karowicz-Bilinska, A., Maszewski, J., & Bartosz, G. (2005). Induction of apoptosis and modulation of production of reactive oxygen species in human endothelial cells by diphenyleneiodonium. Biochemical pharmacology, 69(8), 1263–1273.
2. Baum, J., Ward, R. H., & Conway, D. J. (2002). Natural selection on the erythrocyte surface. Molecular biology and evolution, 19(3), 223–229.
3. Bedard, K., & Krause, K. H. (2007). The NOX family of ROS-generating NADPH oxidases: physiology and pathophysiology. Physiological reviews, 87(1), 245–313.
4. Braun, V., & Niedergang, F. (2006). Linking exocytosis and endocytosis during phagocytosis. Biology of the Cell, 98(3), 195-201.
5. Edberg, J. C., Wright, E., & Taylor, R. P. (1987). Quantitative analyses of the binding of soluble complement-fixing antibody/dsDNA immune complexes to CR1 on human red blood cells. The Journal of Immunology, 139(11), 3739–3747.
6. Fonseca, A. M., Pereira, C. F., Porto, G., & Arosa, F. A. (2003). Red blood cells promote survival and cell cycle progression of human peripheral blood T cells independently of CD58/LFA-3 and heme compounds. Cellular immunology, 224(1), 17–28.
7. Herwald, H., & Egesten, A. (2014). The Janus face of macrophages in immunity. Journal of Innate Immunity, 6(6), 713.
8. Jahejo, A. R., Bukhari, S. A. R., Jia, F. J., Raza, S. H. A., Shah, M. A., Rajput, N., ... & Han, L. X. (2020). Integration of gene expression profile data to screen and verify immune-related genes of chicken erythrocytes involved in Marek's disease virus. Microbial Pathogenesis, 148, 104454.
9. Khan, A., Jahejo, A. R., Qiao, M. L., Han, X. Y., Cheng, Q. Q., Mangi, R. A., ... & Tian, W. X. (2021). NF-кB pathway genes expression in chicken erythrocytes infected with avian influenza virus subtype H9N2. British Poultry Science, 62(5), 666–671.
10. Klei, T. R., Meinderts, S. M., van den Berg, T. K., & van Bruggen, R. (2017). From the cradle to the grave: the role of macrophages in erythropoiesis and erythrophagocytosis. Frontiers in immunology, 8, 73.
11. Klionsky, D. J., Abdelmohsen, K., Abe, A., Abedin, M. J., Abeliovich, H., Adachi, H., ... & Bertolotti, A. (2016). Guidelines for the use and interpretation of assays for monitoring autophagy . Autophagy.
12. Kosecka-Strojek, M., Trzeciak, J., Homa, J., Trzeciak, K., Władyka, B., Trela, M., ... & Lis, M. W. (2021). Effect of Staphylococcus aureus infection on the heat stress protein 70 (HSP70) level in chicken embryo tissues. Poultry Science, 100(6), 101119.
13. Laskin, D. L., Sunil, V. R., Gardner, C. R., & Laskin, J. D. (2011). Macrophages and tissue injury: agents of defense or destruction?. Annual review of pharmacology and toxicology, 51, 267.
14. Lewandowska-Sabat, A. M., Hansen, S. F., Solberg, T. R., Østerås, O., Heringstad, B., Boysen, P., & Olsaker, I. (2018). MicroRNA expression profiles of bovine monocyte-derived macrophages infected in vitro with two strains of Streptococcus agalactiae. BMC genomics, 19(1), 1–15.
15. Li, J., Barreda, D. R., Zhang, Y. A., Boshra, H., Gelman, A. E., LaPatra, S., ... & Sunyer, J. O. (2006). B lymphocytes from early vertebrates have potent phagocytic and microbicidal abilities. Nature immunology, 7(10), 1116–1124.
16. Li, Y. Q., Sun, L., & Li, J. (2018). Internalization of large particles by turbot (Scophthalmus maximus) IgM+ B cells mainly depends on macropinocytosis. Developmental & Comparative Immunology, 82, 31–38.
17. Li, Y. Q., Sun, L., & Li, J. (2019). Macropinocytosis-dependent endocytosis of Japanese flounder IgM+ B cells and its regulation by CD22. Fish & shellfish immunology, 84, 138–147.
18. Liu, L., Zhou, Y., Zhao, X., Wang, H., Wang, L., Yuan, G., ... & Lin, L. (2014). Oligochitosan stimulated phagocytic activity of macrophages from blunt snout bream (Megalobrama amblycephala) associated with respiratory burst coupled with nitric oxide production. Developmental & Comparative Immunology, 47(1), 17–24.
19. Lu, Z., Yang, G., Qin, Z., Shen, H., Zhang, M., Shi, F., ... & Lin, L. (2020). Glutamate related osmoregulation of guanine nucleotide-binding protein G (I) α2 from giant freshwater prawn (Macrobrachium rosenbergii) during molting and salinity stress. Aquaculture, 521, 735000.
20. Mastroeni, P., Vazquez-Torres, A., Fang, F. C., Xu, Y., Khan, S., Hormaeche, C. E., & Dougan, G. (2000). Antimicrobial actions of the NADPH phagocyte oxidase and inducible nitric oxide synthase in experimental salmonellosis. II. Effects on microbial proliferation and host survival in vivo. The Journal of experimental medicine, 192(2), 237–248.
21. Michiels, C., Raes, M., Toussaint, O., & Remacle, J. (1994). Importance of Se-glutathione peroxidase, catalase, and Cu/Zn-SOD for cell survival against oxidative stress. Free radical Biology and medicine, 17(3), 235–248.
22. Minakami, R., & Sumimoto, H. (2006). Phagocytosis-coupled activation of the superoxide-producing phagocyte oxidase, a member of the NADPH oxidase (nox) family. International journal of hematology, 84(3), 193–198.
23. Minasyan, H. (2014). Erythrocyte and blood antibacterial defense. European Journal of Microbiology and Immunology, 4(2), 138–143.
24. Minasyan, H. (2016). Mechanisms and pathways for the clearance of bacteria from blood circulation in health and disease. Pathophysiology, 23(2), 61–66.
25. Øverland, H. S., Pettersen, E. F., Rønneseth, A., & Wergeland, H. I. (2010). Phagocytosis by B-cells and neutrophils in Atlantic salmon (Salmo salar L.) and Atlantic cod (Gadus morhua L.). Fish & shellfish immunology, 28(1), 193–204.
26. Passantino, L., Altamura, M., Cianciotta, A., Patruno, R., Tafaro, A., Jirillo, E., & Passantino, G. F. (2002). Fish immunology. I. Binding and engulfment of Candida albicans by erythrocytes of rainbow trout (Salmo gairdneri Richardson). Immunopharmacology and immunotoxicology, 24(4), 665–678.
27. Porto, B., Fonseca, A. M., Godinho, I., Arosa, F. A., & Porto, G. (2001). Human red blood cells have an enhancing effect on the relative expansion of CD8+ T lymphocytes in vitro. Cell Proliferation, 34(6), 359–367.
Published
2023-03-15
How to Cite
KisilD. О. (2023). ANTIBACTERIAL ACTIVITY OF PHAGOCYTOSIS OF DOMESTIC DUCK ERYTHROCYTES. Bulletin of Sumy National Agrarian University. The Series: Veterinary Medicine, (4(59), 33-37. https://doi.org/10.32845/bsnau.vet.2022.4.5