Staphylococcus aureus avirulent mutant vaccine induces humoral and cellular immune responses on pregnant heifers

Vaccine

Volumn 34, Issue 29, 2016, Pages 3356-3362

  Pellegrino, M ^a,b   Rodriguez, N ^a   Vivas, A ^a   Giraudo, J ^a   Bogni, C ^a  

^a DEPARTAMENTO DE QUÍMICA   (Argentina)

^b Facultad de Ciencias Naturales e Instituto M Lillo   (Argentina)

Author keywords

Avirulent mutant; Bovine mastitis; Staphylococcus aureus

Indexed keywords

GAMMA INTERFERON; IMMUNOGLOBULIN G; IMMUNOGLOBULIN G1; IMMUNOGLOBULIN G2; INTERLEUKIN 13; STAPHYLOCOCCUS AUREUS AVIRULENT MUTANT VACCINE; STAPHYLOCOCCUS VACCINE; UNCLASSIFIED DRUG; BACTERIUM ANTIBODY; CYTOKINE; LIVE VACCINE;

ANIMAL EXPERIMENT; ARTICLE; BACTERIAL GROWTH; BACTERICIDAL ACTIVITY; CELLULAR IMMUNITY; COLONY FORMING UNIT; COLOSTRUM; CONTROLLED STUDY; FEMALE; HEIFER; HUMORAL IMMUNITY; LYMPHOCYTE PROLIFERATION; NONHUMAN; PRIORITY JOURNAL; STAPHYLOCOCCUS AUREUS; VACCINATION; ANIMAL; BLOOD; BOVINE; IMMUNOLOGY; MASTITIS, BOVINE; MICROBIOLOGY; MILK; PREGNANCY; RANDOMIZED CONTROLLED TRIAL;

ANIMALS; ANTIBODIES, BACTERIAL; CATTLE; CYTOKINES; FEMALE; IMMUNITY, CELLULAR; IMMUNITY, HUMORAL; IMMUNOGLOBULIN G; MASTITIS, BOVINE; MILK; PREGNANCY; SERUM BACTERICIDAL TEST; STAPHYLOCOCCAL VACCINES; STAPHYLOCOCCUS AUREUS; VACCINES, ATTENUATED;

EID: 84971641056     PISSN: 0264410X     EISSN: 18732518     Source Type: Journal    
DOI: 10.1016/j.vaccine.2016.05.014     Document Type: Article

References (40)

1. [1] Fetrow, J., Mastitis: an economic consideration. Proc 29th Annu Meet Natl Mastit Counc, Atlanta, GA, 2000, 3–47.
2. [2] Bogni, C., Odierno, L., Raspanti, C., Giraudo, J., Larriestra, A., Reinoso, E., et al. War against mastitis: current concepts on controlling bovine mastitis pathogens. Méndez Vilas, A., (eds.) Science against microbial pathogens: communicating current research and technological advances, 2011, FORMATEX Inc, Spain, 483–494.
3. [3] Whist, A.C., Østerås, O., Associations between somatic cell counts at calving or prior to drying-off and clinical mastitis in the remaining or subsequent lactation. J Dairy Res 74 (2007), 66–73.
4. [4] Gill, J.J., Pacan, J.C., Carson, M.E., Leslie, K.E., Griffiths, M.W., Sabour, P.M., Efficacy and pharmacokinetics of bacteriophage therapy in treatment of subclinical Staphylococcus aureus mastitis in lactating dairy cattle. Antimicrob Agents Chemother 50 (2006), 2912–2918, 10.1128/AAC.01630-05.
5. [5] Vissio, C., Dieser, S., Raspanti, C., Giraudo, J., Bogni, C., Odierno, L., et al. Dairy herd mastitis program in Argentina: farm clusters and effects on bulk milk somatic cell counts. Pak Vet J 33 (2013), 80–84.
6. [6] Russi, N.B., Maito, J., Dieser, S.a., Renna, M.S., Signorini, M.L., Camussone, C., et al. Comparison of phenotypic tests for detecting penicillin G resistance with presence of blaZ gene in Staphylococcus aureus isolated from bovine intramammary infections. J Dairy Res 82 (2015), 317–321, 10.1017/S0022029915000242.
7. [7] Sordillo, L.M., Factors affecting mammary gland immunity and mastitis susceptibility. Livest Prod Sci 98 (2005), 89–99, 10.1016/j.livprodsci.2005.10.017.
8. [8] Alnakip, M.E., Quintela-baluja, M., Böhme, K., Fernández-no, I., Caamaño-antelo, S., Calo-mata, P., et al. The immunology of mammary gland of dairy ruminants between healthy and inflammatory conditions. J Vet Med, 2014, 2–31.
9. [9] McDougall, S., Parker, K.I., Heuer, C., Compton, C.W.R., A review of prevention and control of heifer mastitis via non-antibiotic strategies. Vet Microbiol 134 (2009), 177–185, 10.1016/j.vetmic.2008.09.026.
10. [10] Pantoja, J.C.F., Hulland, C., Ruegg, P.L., Dynamics of somatic cell counts and intramammary infections across the dry period. Prev Vet Med 90 (2009), 43–54, 10.1016/j.prevetmed.2009.03.012.
11. [11] Leitner, G., Krifucks, O., Kiran, M.D., Balaban, N., Vaccine development for the prevention of staphylococcal mastitis in dairy cows. Vet Immunol Immunopathol 142 (2011), 25–35, 10.1016/j.vetimm.2011.03.023.
12. [12] Frola, I.D., Pellegrino, M.S., Espeche, M.C., Giraudo, J.a., Nader-Macias, M.E., Bogni, C.I., Effects of intramammary inoculation of Lactobacillus perolens CRL1724 in lactating cows’ udders. J Dairy Res 79 (2012), 84–92, 10.1017/S0022029911000835.
13. [13] Fejzić, N., Begagić, M., Šerić-haračić, S., Smajlović, M., Beta lactam antibiotics residues in cow's milk: comparison of efficacy of three screening tests used in Bosnia and Herzegovina. Bosn J Basic Med Sci 14 (2014), 155–159.
14. [14] Middleton, J.R., Luby, C.D., Adams, D.S., Efficacy of vaccination against staphylococcal mastitis: a review and new data. Vet Microbiol 134 (2009), 192–198, 10.1016/j.vetmic.2008.09.053.
15. [15] Pereira, U.P., Oliveira, D.G.S., Mesquita, L.R., Costa, G.M., Pereira, L.J., Efficacy of Staphylococcus aureus vaccines for bovine mastitis: a systematic review. Vet Microbiol 148 (2011), 117–124, 10.1016/j.vetmic.2010.10.003.
16. [16] Sykes, K., Progress in the development of genetic immunization. Expert Rev Vac 7 (2008), 1395–1404.
17. [17] Brown, W., Rice-Ficht, A.C., Estes, D.M., Bovine type 1 and type 2 responses. Vet Immunol Immunopathol 63 (1998), 45–55, 10.1016/S0165-2427(98)00081-6.
18. [18] Wellnitz, O., Bruckmaier, R.M., The innate immune response of the bovine mammary gland to bacterial infection. Vet J 192 (2012), 148–152, 10.1016/j.tvjl.2011.09.013.
19. [19] Mosmann, T.R., Cherwinski, H., Bond, M.W., Giedlin, Ma, Coffman, R.L., Two types of murine helper T cell clone. I. Definition according to profiles of lymphokine activities and secreted proteins. J Immunol 136 (1986), 2348–2357, 10.1111/j.1442-9071.2011.02672.x.
20. [20] Cher, D., Mosmann, T., Two types of murine helper T cell clone. II. Delayed-type hypersensitivity is mediated by TH1 clones. J Immunol 138 (1987), 3688–3694.
21. [21] Lucey, D., Evolution of the type-1 (Th1)-type-2 (Th2) cytokine paradigm. Infect Dis Clin North Am 13 (1999), 1–9.
22. [22] Romagnani, S., Th1/Th2 cells. Inflamm Bowel Dis 5 (1999), 285–294.
23. [23] Riollet, C., Rainard, P., Poutrel, B., Cells and cytokines in inflammatory secretions of bovine mammary gland. Adv Exp Med Biol 480 (2000), 247–258.
24. [24] Oviedo-Boyso, J., Valdez-Alarcón, J.J., Cajero-Juárez, M., Ochoa-Zarzosa, A., López-Meza, J.E., Bravo-Patiño, A., et al. Innate immune response of bovine mammary gland to pathogenic bacteria responsible for mastitis. J Infect 54 (2007), 399–409, 10.1016/j.jinf.2006.06.010.
25. [25] Pellegrino, M., Giraudo, J., Raspanti, C., Nagel, R., Odierno, L., Primo, V., et al. Experimental trial in heifers vaccinated with Staphylococcus aureus avirulent mutant against bovine mastitis. Vet Microbiol 127 (2008), 186–190.
26. [26] Deb, R., Kumar, A., Chakraborty, S., Verma, A.K., Tiwari, R., Dhama, K., et al. Trends in diagnosis and control of bovine mastitis: a review. Pak J Biol Sci 16 (2013), 1653–1661, 10.3923/pjbs.2013.1653.1661.
27. [27] Pellegrino, M., Giraudo, J., Raspanti, C., Odierno, L., Bogni, C., Efficacy of immunization against bovine mastitis using a Staphylococcus aureus avirulent mutant vaccine. Vaccine 28 (2010), 4523–4528, 10.1016/j.vaccine.2010.04.056.
28. [28] National Mastitis Council, Microbiological procedures for the diagnosis of bovine udder infection and determination of milk quality. 4th ed., 2004, W. D. Hoard and Sons Co.
29. [29] Bogni, C., Segura, M., Giraudo, J., Giraudo a, Calzolari a, Nagel, R., Avirulence and immunogenicity in mice of a bovine mastitis Staphylococcus aureus mutant. Can J Vet Res 62 (1998), 293–298.
30. [30] Aldridge, B., Garry, F., Adams, R., Role of colostral transfer in neonatal calf management: failure of acquisition of passive immunity. Compend Contin Educ Pract Vet 14 (1992), 265–270.
31. [31] Almeida, R., Matthews, K., Cifrian, E., Guidry, A., Oliver, S., Staphylococcus aureus invasion of bovine mammary epithelial cells. J Dairy Sci 79 (1996), 1021–1026.
32. [32] Hensen, S.M., Pavičić MJAMP, Lohuis, J.A.C.M., Poutrel, B., Use of bovine primary mammary epithelial cells for the comparison of adherence and invasion ability of Staphylococcus aureus strains. J Dairy Sci 83 (2000), 418–429.
33. [33] Wei, Z., Fu, Y., Zhou, E., Tian, Y., Yao, M., Li, Y., et al. Effects of niacin on Staphylococcus aureus internalization into bovine mammary epithelial cells by modulating NF-κB activation. Microb Pathog 71–72 (2014), 62–67, 10.1016/j.micpath.2014.03.005.
34. [34] Burton, J.L., Kehrli, M.E.J., Effects of dexamethasone on bovine circulating T lymphocyte populations. J Leukoc Biol 59 (1996), 90–99.
35. [35] Hoshino, S., Wakita, M., Kobayashi, Y., Sakauchi, R., Nishiguchi, Y., Ozawa, A., et al. Variations in serum levels of insulin-like growth factor-1, growth hormone and thyroid hormones during lactation in dairy cows. Comp Biochem Physiol A Comp Physiol 99 (1991), 61–64.
36. [36] Burvenich, C., Paape, M.J., Hoeben, D., Dosogne, H., Massart-Leën, A.M., Blum, J., Modulation of the inflammatory reaction and neutrophil defense of the bovine lactating mammary gland by growth hormone. Domest Anim Endocrinol 17 (1999), 149–159.
37. [37] Buzzola, F.R., Barbagelata, M.S., Caccuri, R.L., Sordelli, D.O., Attenuation and persistence of and ability to induce protective immunity to a Staphylococcus aureus aroA mutant in mice. Infect Immun 74 (2006), 3498–3506, 10.1128/IAI.01507-05.
38. [38] Sordillo, L.M., Streicher, K.L., Mammary gland immunity and mastitis susceptibility. J Mamm Gland Biol Neoplasia, 2002, 7.
39. [39] Trigona, W.L., Hirano, A., Brown, W.C., Estes, D.M., Immunoregulatory roles of Interleukin-13 in cattle. J Interf Cytokine Res 19 (2004), 1317–1324.
40. [40] Riollet, C., Rainard, P., Poutrel, B., Kinetics of cells and cytokines during immune-mediated inflammation in the mammary gland of cows systemically immunized with Staphylococcus aureus alpha-toxin. Inflamm Res 49 (2000), 486–496.