Bactericidal activity of macrophages against Streptococcus uberis is different in mammary gland secretions of lactating and drying off cows

Veterinary Immunology and Immunopathology

Volumn 114, Issue 1-2, 2006, Pages 111-120

  Denis, Michel ^a   Parlane, Natalie A ^a   Lacy Hulbert, S Jane ^b   Summers, Emma L ^b   Buddle, Bryce M ^a   Wedlock, D Neil ^a  

^a AGRESEARCH   (New Zealand)

^b Dexcel Limited   (New Zealand)

Author keywords

Cattle; Cytokines; IFN ; Macrophages; Milk; Streptococcus uberis

Indexed keywords

GAMMA INTERFERON; NITRIC OXIDE; TUMOR NECROSIS FACTOR ALPHA;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; BACTERICIDAL ACTIVITY; CELL STIMULATION; CONTROLLED STUDY; COW; LACTATION; MAMMARY GLAND; MASTITIS; MONOCYTE; NONHUMAN; PHAGOCYTOSIS; PROTEIN FOLDING; STAPHYLOCOCCUS AUREUS; STREPTOCOCCUS UBERIS; VIRULENCE;

ANIMALS; CATTLE; ENZYME INHIBITORS; FEMALE; LACTATION; MACROPHAGES; MAMMARY GLANDS, ANIMAL; MASTITIS, BOVINE; MILK; NITRIC OXIDE; OMEGA-N-METHYLARGININE; REACTIVE NITROGEN SPECIES; REACTIVE OXYGEN SPECIES; STAPHYLOCOCCAL INFECTIONS; STAPHYLOCOCCUS; TUMOR NECROSIS FACTOR-ALPHA;

BACTERIA (MICROORGANISMS); BOS TAURUS; STAPHYLOCOCCUS AUREUS; STREPTOCOCCUS UBERIS;

EID: 33748779033     PISSN: 01652427     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.vetimm.2006.08.001     Document Type: Article

References (31)

1. Ali F., Lee M.E., Iannelli F., Pozzi G., Mitchell T.J., Read R.C., and Dockrell D.H. Streptococcus pneumoniae-associated human macrophage apoptosis after bacterial internalization via complement and Fc-gamma receptors correlates with intracellular bacterial load. J. Infect. Dis. 188 (2003) 1119-1131
2. Almeida R.A., and Oliver S.P. Phagocytosis of Streptococcus uberis by bovine mammary macrophages: opsonizing effect of bovine antiserum. Zentralbl. Veterinarmed. B 42 (1995) 331-337
3. Almeida R.A., Fang W., and Oliver S.P. Adherence and internalization of Streptococcus uberis to bovine mammary epithelial cells are mediated by host cell proteoglycans. FEMS Microbiol. Lett. 177 (1999) 313-317
4. Almeida R.A., Luther D.A., and Oliver S.P. Incubation of Streptococcus uberis with extracellular matrix proteins enhances adherence to and internalization into bovine mammary epithelial cells. FEMS Microbiol. Lett. 178 (1999) 81-85
5. Bannerman D.D., Paape M.J., Goff J.P., Kimura K., Lippolis J.D., and Hope J.C. Innate immune response to intramammary infection with Serratia marcescens and Streptococcus uberis. Vet. Res. 35 (2004) 681-700
6. Biondi A., Peri G., Colombo N., Bolis G., and Mantovani A. Antibody-dependent and -independent cytotoxicity of human mononuclear phagocytes: defective stimulation of tumoricidal activity in milk macrophages. Clin. Exp. Immunol. 49 (1982) 701-708
7. Denis M. Interferon-gamma-treated murine macrophages inhibit growth of tubercle bacilli via the generation of reactive nitrogen intermediates. Cell Immunol. 132 (1991) 150-157
8. Dockrell D.H., Marriott H.M., Prince L.R., Ridger V.C., Ince P.G., Hellewell P.G., and Whyte M.K. Alveolar macrophage apoptosis contributes to pneumococcal clearance in a resolving model of pulmonary infection. J. Immunol. 171 (2003) 5380-5388
9. Grant R.G., and Finch J.M. Phagocytosis of Streptococcus uberis by bovine mammary gland macrophages. Res. Vet. Sci. 62 (1997) 74-78
10. Hawkes J.S., Bryan D.L., and Gibson R.A. Cytokine production by human milk cells and peripheral blood mononuclear cells from the same mothers. J. Clin. Immunol. 22 (2002) 338-344
11. Jungi T.W., Valentin-Weigand P., and Brcic M. Differential induction of NO synthesis by gram-positive and gram-negative bacteria and their components in bovine monocyte-derived macrophages. Microb. Pathog. 27 (1999) 43-53
12. Leigh J.A. Streptococcus uberis: a permanent barrier to the control of bovine mastitis?. Vet. J. 157 (1999) 225-238
13. Leigh J.A. Vaccines against bovine mastitis due to Streptococcus uberis: current status and future prospects. Adv. Exp. Med. Biol. 480 (2000) 307-311
14. Leigh J.A., and Field T.R. Streptococcus uberis resists the bactericidal action of bovine neutrophils despite the presence of bound immunoglobulin. Infect. Immun. 62 (1994) 1854-1859
15. Nargi F.E., and Yang T.J. Optimization of the L-M cell bioassay for quantitating tumor necrosis factor alpha in serum and plasma. J. Immunol. Meth. 151 (1993) 81-91
16. Nickerson S.C., and Sordillo L.M. Role of macrophages and multinucleate giant cells in the resorption of corpora amylacea in the involuting bovine mammary gland. Cell Tissue Res. 240 (1985) 394-397
17. Otani H., and Futakami M. Effects of bovine milk proteins on the phagocytic property and formation of nitrite by mouse peritoneal macrophages. Anim. Sci. Technol. 65 (1994) 423-431
18. Otani H., and Futakami M. Modification of nitrite production and phagocytosis of thioglycollate-elicited mouse peritoneal macrophages by bovine casein digests. Food Agric. Immunol. 8 (1996) 59-69
19. Otani H., and Hata I. Inhibition of proliferative responses of mouse spleen lymphocytes and rabbit Peyer's patch cells by bovine milk caseins and their digests. J. Dairy Res. 62 (1995) 339-348
20. Paape M.J., Shafer-Weaver K., Capuco A.V., Van Oostveldt K., and Burvenich C. Immune surveillance of mammary tissue by phagocytic cells. Adv. Exp. Med. Biol. 480 (2000) 259-277
21. Pedersen L.H., Aalbæk B., Røntved C.M., Ingvartsen K.L., Sorensen N.S., Heegaard P.M.H., and Jensen H.E. Early pathogenesis and inflammatory response in experimental bovine mastitis due to Streptococcus uberis. J. Comp. Pathol. 128 (2003) 156-164
22. Pighetti G.M., and Sordillo L.M. Regulation of mammary gland macrophage tumour necrosis factor-alpha production with interferon-gamma. Res. Vet. Sci. 56 (1994) 252-255
23. Politis I., McBride B.W., Burton J.H., Zhao X., and Turner J.D. Secretion of interleukin-1 by bovine milk macrophages. Am. J. Vet. Res. 52 (1991) 858-862
24. Rambeaud M., Almeida R.A., Pighetti G.M., and Oliver S.P. Dynamics of leukocytes and cytokines during experimentally induced Streptococcus uberis mastitis. Vet. Immunol. Immunopathol. 96 (2003) 193-205
25. Riollet C., Rainard P., and Poutrel B. Cells and cytokines in inflammatory secretions of bovine mammary gland. Adv. Exp. Med. Biol. 480 (2000) 247-258
26. Rivas R.A., el-Mohandes A.A., and Katona I.M. Mononuclear phagocytic cells in human milk: HLA-DR and Fc gamma R ligand expression. Biol. Neonate 66 (1994) 195-204
27. Rook G.A., Steele J., Umar S., and Dockrell H.M. A simple method for the solubilisation of reduced NBT, and its use as a colorimetric assay for activation of human macrophages by gamma-interferon. J. Immunol. Meth. 82 (1985) 161-167
28. Seegers H., Fourichon C., and Beaudeau F. Production effects related to mastitis and mastitis economics in dairy cattle herds. Vet. Res. 34 (2003) 475-491
29. Shiloh M.U., MacMicking J.D., Nicholson S., Brause J.E., Potter S., Marino M., Fang F., Dinauer M., and Nathan C. Phenotype of mice and macrophages deficient in both phagocyte oxidase and inducible nitric oxide synthase. Immunity 10 (1999) 29-38
30. Subiza J.L., Rodriguez C., Figueredo A., Mateos P., Alvarez R., and de la Concha E.G. Impaired production and lack of secretion of interleukin 1 by human breast milk macrophages. Clin. Exp. Immunol. 71 (1988) 493-496
31. Thomas L.H., Haider W., Hill A.W., and Cook R.S. Pathologic findings of experimentally induced Streptococcus uberis infection in the mammary gland of cows. Am. J. Vet. Res. 55 (1994) 1723-1728