Immune Responses in Mice Immunized with Mastitis Multiple Vaccines Using Different Adjuvants
DOI:
https://doi.org/10.22456/1679-9216.84088Abstract
Background: Bovine mastitis, a serious disease associated with both high incidence and significant economic losses, posing a major challenge to the global dairy industry. The development of vaccines for protection from new infections by mastitis pathogens is of considerable interest to the milk production industry. Vaccination is a common and easy strategy for the control of infectious diseases, and the adjuvants used in the formulation is a critical factor for vaccine efficacy improvement. The main objective of the present study was to evaluate three different adjuvants for their ability to enhance immune responses of mice that vaccinated with Bovine Mastitis Multiple Vaccine.
Materials, Methods & Results: The thymus and spleen index, the phagocytic ability of macrophage and the serum antibody levels of mice were detected after vaccination, respectively. The results showed that the thymus index, spleen index, and the phagocytic ability of macrophage of mice in Aluminum group exhibited a significant higher level (P < 0.05) compared with those in the control groups. The difference of the serum antibody levels was significant (P < 0.05) between experimental groups and control group after vaccination. The serum antibody concentration of mice in FIA group was higher compared with other groups and had a longer duration. The antibody concentration of mice in France 206 oil group can not increase as fast as the antibody concentration of Aluminum group, but it can last a longer time at a high level. In conclusion, multiple vaccines mixed with three different adjuvants could enhance the immunity of mice and Freund’s incomplete adjuvant is the best choice for this vaccine.
Discussion: Adjuvants play an important role in increasing the efficacy of a number of different vaccines. In this study, three kinds of adjuvants (Aluminum hydroxide, France 206 oil and FIA) were evaluated for their adjuvant effects for multiple vaccine of bovine mastitis in mice and aluminum hydroxide did best as the vaccine adjuvant from the results. Aluminum hydroxide is a universally accepted adjuvant for both human and veterinary vaccines. The goal of vaccination is to generate strong immune response providing protection against infection for a time. Different protective effects will usually obtained by different adjuvants even use same antigen. In this work, FIA, Alum and 206 oil were chosen as adjuvants for inactivated antigens of Streptococcus agalactiae, Streptococcus dysgalactiae and Staphylococcus aureus. The results showed that there was a significantly higher antibody levels in vaccinated mice compared with those in control group. In addition, the mice in France 206 oil and FIA group performed a higher antibody levels and stronger immunity than mice in Aluminum hydroxide groups. These findings suggest that Freund’s incomplete adjuvant (FIA) would be the best candidate as the adjuvant for mastitis multiple vaccines investigated in this study.
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References
Aguilar J.C. & Rodríguez E.G. 2007. Vaccine Adjuvants Revisited. Vaccine. 25(19): 3752-3762.
Blowey R.W. & Edmondson P. 2010. Mastitis Control in Dairy Herds. 2nd edn. Wallingford: CABI, pp.1-10.
Bronte V. & Pittet M. 2013. The Spleen in Local and Systemic Regulation of Immunity. Immunity. 39(5): 806-818.
Changklungmoa N., Phoinok N., Yencham C., Sobhon P. & Kueakhai P. 2016. Vaccine Potential of Recombinant CathepsinL1G against Fasciola Gigantica in Mice. Veterinary Parasitology. 226(2016): 124-131.
Chen L., Li S., Wang Z., Chang R., Su J. & Han B. 2012. Protective Effect of Recombinant Staphylococcal Enterotoxin an Entrapped in Polylactic-co-glycolic Acid Microspheres Against Staphylococcus aureus Infection. Veterinary Research. 43(1): 20.
D'agata E.M., Dupont-rouzeyrol M., Magal P., Olivier D. & Ruan S. 2008. The Impact of Different Antibiotic Regimens on the Emergence of Antimicrobial-resistant Bacteria. Plos One. 3(12): 1165-1165.
Duan X., Li J., Zhang Y., Li W., Zhao L., Nie H., Sun G. & Li B. 2015. Activation of Nrf2 Pathway in Spleen, Thymus as Well as Peripheral Blood Mononuclear Cells by Acute Arsenic Exposure in Mice. International Immunopharmacology. 28(2): 1059-1067.
Fleck J.D., Kauffmann C., Spilki F., Lencina C.L., Roehe P.M. & Gosmann G. 2006. Adjuvant Activity of Quillaja Brasiliensis Saponins on the Immune Responses to Bovine Herpesvirus Type 1 in Mice. Vaccine. 49: 7129-7134.
Fuchs J., Chu H., O’day P., Pyles R., Bourne N., Das S.C., Milligan G.N., Barrett A.D., Partidos C.D. & Osorio J.E. 2014. Investigating the Efficacy of Monovalent and Tetravalent Dengue Vaccine Formulations against Denv-4 Challenge in Ag129 Mice. Vaccine. 32(48): 6537-6543.
Hartree E.F. 1972. Determination of Protein: a Modification of the Lowry Method That Gives a Linear Photometric Response. Analytical Biochemistry. 48(2): 422-427.
Holland J.K., Hadrich J.C., Wolf C.A. & Lombard J. 2015. Economics of Measuring Costs Due to Mastitis-related Milk Loss. In: Aaea & Waea Joint Annual Meeting (San Francisco, USA). pp.1-18.
Hu S., Concha C., Lin F. & Persson Waller K. 2003. Adjuvant Effect of Ginseng Extracts on the Immune Responses to Immunisation Against Staphylococcus aureus in Dairy Cattle. Veterinary Immunology and Immunopathology. 91(1): 29-37.
Khan F.U., Ihsan A.U., Nawaz W., Khan M.Z., Yang M., Wang G., Liao X., Han L. & Zhou X. 2017. A Novel Mouse Model of Chronic Prostatitis/chronic Pelvic Pain Syndrome Induced by Immunization of Special Peptide Fragment with Aluminum Hydroxide Adjuvant. Immunology Letters. 187: 61-67.
Kuper C.F., Van bilsen J., Cnossen H., Houben G., Garthoff J. & Wolterbeek A. 2016. Development of Immune Organs and Functioning in Humans and Test Animals: Implications for Immune Intervention Studies. Reproductive Toxicology. 64: 180-190.
Kyung P.Y., Fox L.K., Hancock D.D., Wade M.M. & Ho P.Y. 2012. Prevalence and Antibiotic Resistance of Mastitis Pathogens Isolated From Dairy Herds Transitioning to Organic Management. Journal of Veterinary Science. 103-105.
Leelahapongsathon K., Schukken Y. & Suriyasathaporn W. 2014. Quarter, Cow, and Farm Risk Factors for Intramammary Infections with Major Pathogens Relative to Minor Pathogens in Thai Dairy Cows. Tropical Animal Health & Production. 46(6): 1067-1078.
Leitner G., Lubashevsky E., Glickman A., Winkler M., Saran A. & Trainin Z. 2003. Development of a Staphylococcus aureus Vaccine Against Mastitis in Dairy Cows: I. Challenge Trials. Veterinary Immunology and Immunopathology. 93(2): 31-38.
Li J., Xu Y., Wang X., Li Y., Wang L. & Li X. 2016. Construction and Characterization of a Highly Reactive Chicken-derived Single-chain Variable Fragment (scfv) Antibody against Staphylococcus aureus Developed with the T7 Phage Display System. International Immunopharmacology. 35(1): 149-154.
Li W., Li L., Zhen W., Wang L., Pan M., Lv J., Wang F., Yao Y., Nie S. & Xie M. 2017. Ganoderma atrum Polysaccharide Ameliorates Ros Generation and Apoptosis in Spleen and Thymus of Immunosuppressed Mice. Food and Chemical Toxicology. 99: 199-208.
Lögdberg L., Cigén R. & Berggård I. 2009. Th1-th17 Cells Mediate Protective Adaptive Immunity against Staphylococcus aureus and Candida albicans Infection in Mice. Plos Pathogens. 5(12): 5.
Mcconnell M.J. & Pachón J. 2010. Active and Passive Immunization against Acinetobacter baumannii Using an Inactivated Whole Cell Vaccine. Vaccine. 29(1): 1.
Oliver S.P. & Murinda S.E. 2012. Antimicrobial Resistance of Mastitis Pathogens. Veterinary Clinics of North America: Food Animal Practice. 28(2): 165-185.
Östensson K., Lam V., Sjögren N. & Wredle E. 2013. Prevalence of Subclinical Mastitis and Isolated Udder Pathogens in Dairy Cows in Southern Vietnam. Tropical Animal Health & Production. 45(4): 979-986.
Patil H.P., Murugappan S., De vries-idema J., Meijerhof T., De haan A., Frijlink H.W., Wilschut J., Hinrichs W.L. & Huckriede A. 2015. Comparison of Adjuvants for a Spray Freeze-dried Whole Inactivated Virus Influenza Vaccine for Pulmonary Administration. European Journal of Pharmaceutics and Biopharmaceutics. 93(2015): 231-241.
Pellegrino M., Giraudo J., Raspanti C., Odierno L. & Bogni C. 2010. Efficacy of Immunization Against Bovine Mastitis Using a Staphylococcus aureus Avirulent Mutant Vaccine. Vaccine. 28(28): 4523-4528.
Petrovsky N. & Aguilar J.C. 2004. Vaccine Adjuvants: Current State and Future Trends. Immunology & Cell Biology. 82(5): 488.
Rimaniol A.C., Gras G. & Clayette P. 2007. In Vitro Interactions Between Macrophages and Aluminum-containing Adjuvants. Vaccine. 25(37): 6784-6792.
Rimaniol A.C., Gras G., Verdier F., Capel F., Grigoriev V.B., Porcheray F., Sauzeat E., Fournier J.G., Clayette P. & Siegrist C.A. 2004. Aluminum Hydroxide Adjuvant Induces Macrophage Differentiation Towards a Specialized Antigen-presenting Cell Type. Vaccine. 22(23): 3127-3135.
Talbot B.G. & Lacasse P. 2005. Progress in the Development of Mastitis Vaccines. Livest Science. 98(1): 101-113.
Vandenborne B., Van schaik G., Lam T.J.G.M. & Nielen M. 2010. Variation in Herd Level Mastitis Indicators Between Primi- and Multiparae in Dutch Dairy Herds. Preventive Veterinary Medicine. 96(1): 49-55.
Valtulini S., Macchi C., Ballanti P., Cherel Y., Laval A., Theaker J.M., Bak M., Ferretti E. & Morvan H. 2005. Aluminium Hydroxide-induced Granulomas in Pigs. Vaccine. 23(30): 3999-4004.
Weng X.G., Song Q.J., Wu Q., Liu M.C. Wang M.L. & Wang J.F. 2015. Genetic characterization of bovine viral diarrhea virus strains in Beijing, China and innate immune responses of peripheral blood mononuclear cells in persistently infected dairy cattle. Journal of Veterinary Science. 4: 491-500.
Yang B., Xiao B. & Sun T. 2013. Antitumor and Immunomodulatory Activity of Astragalus membranaceus Polysaccharides in H22 Tumor-bearing Mice. International Journal of Biological Macromolecules. 62(11): 287-290.
Zecconi A., Piccinini R. & Fox L.K. 2003. Epidemiologic Study of Intramammary Infections with Staphylococcus aureus During a Control Program in Nine Commercial Dairy Herds. Journal of the American Veterinary Medical Association. 223(5): 684-686.
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