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

Bovine mastitis produces economic losses, attributable to the decrease in milk production, reduced milk quality, costs of treatment and replacement of animals. A successful prophylactic vaccine against Staphylococcus aureus should elicit both humoral and cellular immune responses. In a previous repo...

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Autor principal: Pellegrino, M.
Otros Autores: Rodriguez, N., Vivas, A., Giraudo, J., Bogni, C.
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: Elsevier Ltd 2016
Acceso en línea:Registro en Scopus
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100 1 |a Pellegrino, M. 
245 1 0 |a Staphylococcus aureus avirulent mutant vaccine induces humoral and cellular immune responses on pregnant heifers 
260 |b Elsevier Ltd  |c 2016 
270 1 0 |m Bogni, C.; Departamento de Microbiología e Inmunología, Facultad de Ciencias Exactas, Físico-Químicas y Naturales, Universidad Nacional de Río Cuarto, Ruta 36 Km 601, X5804ZAB Río Cuarto, Argentina; email: cbogni@exa.unrc.edu.ar 
506 |2 openaire  |e Política editorial 
504 |a Fetrow, J., Mastitis: an economic consideration (2000) Proc 29th Annu Meet Natl Mastit Counc, Atlanta, GA, pp. 3-47 
504 |a Bogni, C., Odierno, L., Raspanti, C., Giraudo, J., Larriestra, A., Reinoso, E., War against mastitis: current concepts on controlling bovine mastitis pathogens (2011) Science against microbial pathogens: communicating current research and technological advances, pp. 483-494. , A. Méndez Vilas FORMATEX Inc Spain 
504 |a 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 (2007) J Dairy Res, 74, pp. 66-73 
504 |a 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 (2006) Antimicrob Agents Chemother, 50, pp. 2912-2918 
504 |a Vissio, C., Dieser, S., Raspanti, C., Giraudo, J., Bogni, C., Odierno, L., Dairy herd mastitis program in Argentina: farm clusters and effects on bulk milk somatic cell counts (2013) Pak Vet J, 33, pp. 80-84 
504 |a Russi, N.B., Maito, J., Dieser, S.A., Renna, M.S., Signorini, M.L., Camussone, C., Comparison of phenotypic tests for detecting penicillin G resistance with presence of blaZ gene in Staphylococcus aureus isolated from bovine intramammary infections (2015) J Dairy Res, 82, pp. 317-321 
504 |a Sordillo, L.M., Factors affecting mammary gland immunity and mastitis susceptibility (2005) Livest Prod Sci, 98, pp. 89-99 
504 |a Alnakip, M.E., Quintela-baluja, M., Böhme, K., Fernández-no, I., Caamaño-antelo, S., Calo-mata, P., The immunology of mammary gland of dairy ruminants between healthy and inflammatory conditions (2014) J Vet Med, pp. 2-31 
504 |a McDougall, S., Parker, K.I., Heuer, C., Compton, C.W.R., A review of prevention and control of heifer mastitis via non-antibiotic strategies (2009) Vet Microbiol, 134, pp. 177-185 
504 |a Pantoja, J.C.F., Hulland, C., Ruegg, P.L., Dynamics of somatic cell counts and intramammary infections across the dry period (2009) Prev Vet Med, 90, pp. 43-54 
504 |a Leitner, G., Krifucks, O., Kiran, M.D., Balaban, N., Vaccine development for the prevention of staphylococcal mastitis in dairy cows (2011) Vet Immunol Immunopathol, 142, pp. 25-35 
504 |a 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 (2012) J Dairy Res, 79, pp. 84-92 
504 |a 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 (2014) Bosn J Basic Med Sci, 14, pp. 155-159 
504 |a Middleton, J.R., Luby, C.D., Adams, D.S., Efficacy of vaccination against staphylococcal mastitis: a review and new data (2009) Vet Microbiol, 134, pp. 192-198 
504 |a 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 (2011) Vet Microbiol, 148, pp. 117-124 
504 |a Sykes, K., Progress in the development of genetic immunization (2008) Expert Rev Vac, 7, pp. 1395-1404 
504 |a Brown, W., Rice-Ficht, A.C., Estes, D.M., Bovine type 1 and type 2 responses (1998) Vet Immunol Immunopathol, 63, pp. 45-55 
504 |a Wellnitz, O., Bruckmaier, R.M., The innate immune response of the bovine mammary gland to bacterial infection (2012) Vet J, 192, pp. 148-152 
504 |a Mosmann, T.R., Cherwinski, H., Bond, M.W., Giedlin, M., Coffman, R.L., Two types of murine helper T cell clone. I. Definition according to profiles of lymphokine activities and secreted proteins (1986) J Immunol, 136, pp. 2348-2357 
504 |a Cher, D., Mosmann, T., Two types of murine helper T cell clone. II. Delayed-type hypersensitivity is mediated by TH1 clones (1987) J Immunol, 138, pp. 3688-3694 
504 |a Lucey, D., Evolution of the type-1 (Th1)-type-2 (Th2) cytokine paradigm (1999) Infect Dis Clin North Am, 13, pp. 1-9 
504 |a Romagnani, S., Th1/Th2 cells (1999) Inflamm Bowel Dis, 5, pp. 285-294 
504 |a Riollet, C., Rainard, P., Poutrel, B., Cells and cytokines in inflammatory secretions of bovine mammary gland (2000) Adv Exp Med Biol, 480, pp. 247-258 
504 |a Oviedo-Boyso, J., Valdez-Alarcón, J.J., Cajero-Juárez, M., Ochoa-Zarzosa, A., López-Meza, J.E., Bravo-Patiño, A., Innate immune response of bovine mammary gland to pathogenic bacteria responsible for mastitis (2007) J Infect, 54, pp. 399-409 
504 |a Pellegrino, M., Giraudo, J., Raspanti, C., Nagel, R., Odierno, L., Primo, V., Experimental trial in heifers vaccinated with Staphylococcus aureus avirulent mutant against bovine mastitis (2008) Vet Microbiol, 127, pp. 186-190 
504 |a Deb, R., Kumar, A., Chakraborty, S., Verma, A.K., Tiwari, R., Dhama, K., Trends in diagnosis and control of bovine mastitis: a review (2013) Pak J Biol Sci, 16, pp. 1653-1661 
504 |a Pellegrino, M., Giraudo, J., Raspanti, C., Odierno, L., Bogni, C., Efficacy of immunization against bovine mastitis using a Staphylococcus aureus avirulent mutant vaccine (2010) Vaccine, 28, pp. 4523-4528 
504 |a National Mastitis Council, Microbiological procedures for the diagnosis of bovine udder infection and determination of milk quality (2004), 4th ed. W. D. Hoard and Sons Co; Bogni, C., Segura, M., Giraudo, J., Giraudo a, Calzolari a, Nagel, R., Avirulence and immunogenicity in mice of a bovine mastitis Staphylococcus aureus mutant (1998) Can J Vet Res, 62, pp. 293-298 
504 |a Aldridge, B., Garry, F., Adams, R., Role of colostral transfer in neonatal calf management: failure of acquisition of passive immunity (1992) Compend Contin Educ Pract Vet, 14, pp. 265-270 
504 |a Almeida, R., Matthews, K., Cifrian, E., Guidry, A., Oliver, S., Staphylococcus aureus invasion of bovine mammary epithelial cells (1996) J Dairy Sci, 79, pp. 1021-1026 
504 |a 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 (2000) J Dairy Sci, 83, pp. 418-429 
504 |a Wei, Z., Fu, Y., Zhou, E., Tian, Y., Yao, M., Li, Y., Effects of niacin on Staphylococcus aureus internalization into bovine mammary epithelial cells by modulating NF-κB activation (2014) Microb Pathog, 71–72, pp. 62-67 
504 |a Burton, J.L., Kehrli, M.E.J., Effects of dexamethasone on bovine circulating T lymphocyte populations (1996) J Leukoc Biol, 59, pp. 90-99 
504 |a Hoshino, S., Wakita, M., Kobayashi, Y., Sakauchi, R., Nishiguchi, Y., Ozawa, A., Variations in serum levels of insulin-like growth factor-1, growth hormone and thyroid hormones during lactation in dairy cows (1991) Comp Biochem Physiol A Comp Physiol, 99, pp. 61-64 
504 |a 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 (1999) Domest Anim Endocrinol, 17, pp. 149-159 
504 |a 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 (2006) Infect Immun, 74, pp. 3498-3506 
504 |a Sordillo, L.M., Streicher, K.L., Mammary gland immunity and mastitis susceptibility (2002) J Mamm Gland Biol Neoplasia, p. 7 
504 |a Trigona, W.L., Hirano, A., Brown, W.C., Estes, D.M., Immunoregulatory roles of Interleukin-13 in cattle (2004) J Interf Cytokine Res, 19, pp. 1317-1324 
504 |a 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 (2000) Inflamm Res, 49, pp. 486-496 
520 3 |a Bovine mastitis produces economic losses, attributable to the decrease in milk production, reduced milk quality, costs of treatment and replacement of animals. A successful prophylactic vaccine against Staphylococcus aureus should elicit both humoral and cellular immune responses. In a previous report we evaluated the effectiveness of a live vaccine to protect heifers against challenge with a virulent strain. In the present study the immunological response of heifers after combined immunization schedule was investigated. In a first experimental trial, heifers were vaccinated with 3 subcutaneous doses of avirulent mutant S. aureus RC122 before calving and one intramammary dose (IMD) after calving. Antibodies concentration in blood, bactericidal effect of serum from vaccinated animals and lymphocyte proliferation was determined. The levels of total IgG, IgG1 and IgG2 in colostrum and the lymphocyte proliferation index were significantly higher in vaccinated respect to non-vaccinated group throughout the experiment. The second trial, where animals were inoculated with different vaccination schedules, was carried out to determine the effect of the IMD on the level of antibodies in blood and milk, cytokines (IL-13 and IFN-γ) concentration and milk's SCC and bacteriology. The bacterial growth of the S. aureus strains was totally inhibited at 1–3 × 106 and 1–3 × 103 cfu/ml, when the strains were mixed with pooled serum diluted 1/40. The results shown that IMD has not a significant effect on the features determinate. In conclusion, a vaccination schedule involving three SC doses before calving would be enough to stimulate antibodies production in milk without an IMD. Furthermore, the results showed a bactericidal effect of serum from vaccinated animals and this provides further evidence about serum functionality. Immune responses, humoral (antigen-specific antibodies and Th2 type cytokines) and cellular (T-lymphocyte proliferation responses and Th1 type cytokines), were augmented by administration of the avirulent mutant which represent an antigenic pool. © 2016 Elsevier Ltd  |l eng 
593 |a Departamento de Microbiología e Inmunología, Facultad de Ciencias Exactas, Físico-Químicas y Naturales, Universidad Nacional de Río Cuarto, Ruta 36 Km 601, X5804ZAB Río Cuarto, Córdoba, Argentina 
593 |a Departamento de Biología Molecular, Facultad de Ciencias Exactas, Físico-Químicas y Naturales, Universidad Nacional de Río Cuarto, Ruta 36 Km 601, X5804ZAB Río Cuarto, Córdoba, Argentina 
593 |a Departamento de Anatomía Animal, Facultad de Agronomía y Veterinaria, Universidad Nacional de Río Cuarto, Ruta 36 Km 601, X5804ZAB Río Cuarto, Córdoba, Argentina 
593 |a Departamento de Patología Animal, Facultad de Agronomía y Veterinaria, Universidad Nacional de Río Cuarto, Ruta 36 Km 601, X5804ZAB Río Cuarto, Córdoba, Argentina 
593 |a Member of Consejo Nacional de Investigaciones Científicas y Tecnológicas (CIC-CONICET), Buenos Aires, Argentina 
690 1 0 |a AVIRULENT MUTANT 
690 1 0 |a BOVINE MASTITIS 
690 1 0 |a STAPHYLOCOCCUS AUREUS 
700 1 |a Rodriguez, N. 
700 1 |a Vivas, A. 
700 1 |a Giraudo, J. 
700 1 |a Bogni, C. 
773 0 |d Elsevier Ltd, 2016  |g v. 34  |h pp. 3356-3362  |k n. 29  |x 0264410X  |w (AR-BaUEN)CENRE-7118  |t Vaccine 
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