The role of CD14 during resolution of experimentally induced Staphylococcus aureus and Streptococcus uberis mastitis

Comparative Immunology, Microbiology and Infectious Diseases

Volumn 29, Issue 4, 2006, Pages 243-262

  Sladek, Z ^a   Rysanek, D ^b  

^a MENDEL UNIVERSITY IN BRNO   (Czech Republic)

^b VETERINARY RESEARCH INSTITUTE   (Czech Republic)

Author keywords

Cd14; Macrophages; Mastitis; Neutrophils; Staphylococcus aureus; Streptococcus uberis

Indexed keywords

CD14 ANTIGEN; MONOCLONAL ANTIBODY;

ANIMAL CELL; ANIMAL EXPERIMENT; ANTIGEN EXPRESSION; ARTICLE; CELL VACUOLE; CONTROLLED STUDY; EXPERIMENTAL INFECTION; FEMALE; GRAM NEGATIVE BACTERIUM; GRAM POSITIVE BACTERIUM; IMMUNE RESPONSE; IN VITRO STUDY; INFLAMMATION; MACROPHAGE; MASTITIS; MOLECULAR RECOGNITION; NEUTROPHIL; NEUTROPHILIA; NONHUMAN; STAPHYLOCOCCUS AUREUS; STREPTOCOCCUS UBERIS; TIME;

ANIMALS; ANTIGENS, CD14; APOPTOSIS; CATTLE; FEMALE; FLOW CYTOMETRY; MACROPHAGES; MASTITIS, BOVINE; MICROSCOPY, ELECTRON, TRANSMISSION; NEUTROPHILS; PHAGOCYTOSIS; STAPHYLOCOCCAL INFECTIONS; STAPHYLOCOCCUS AUREUS; STREPTOCOCCAL INFECTIONS; STREPTOCOCCUS;

STAPHYLOCOCCUS AUREUS; STREPTOCOCCUS UBERIS;

EID: 33748466961     PISSN: 01479571     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cimid.2006.06.006     Document Type: Article

References (56)

1. Aderem A., and Ulevitch R.J. Toll-like receptors in the induction of the innate immune response. Nature 17 406 (2000) 782-787
2. Yoshimura A., Lien E., Ingalls R.R., Tuomanen E., Dziarski R., and Golenbock D. Cutting edge: recognition of Gram-positive bacterial cell wall components by the innate immune system occurs via Toll-like receptor 2. J Immunol 163 (1999) 1-5
3. Hajjar A.M., O'Mahony D.S., Ozinsky A., Underhill D.M., Aderem A., Klebanoff S.J., et al. Cutting edge: functional interactions between toll-like receptor (TLR) 2 and TLR1 or TLR6 in response to phenol-soluble modulin. J Immunol 166 (2001) 15-19
4. Schroder K., Hertzog P.J., Ravasi T., and Hume D.A. Interferon-gamma: an overview of signals, mechanisms and functions. J Leukoc Biol 75 (2004) 163-189
5. Beutler B. TLR 4: central component of the sole mammalian LPS sensor. Curr Opin Immunol 12 (2000) 20-26
6. Hirschfeld M., Ma Y., Weis J.H., Vogel S.N., and Weis J.J. Cutting edge: repurification of lipopolysaccharide eliminates signaling through both human and murine toll-like receptor 2. J Immunol 165 (2000) 618-622
7. Goldammer T., Zerbe H., Molenaar A., Schuberth H.J., Brunner R.M., Kata S.R., et al. Mastitis increases mammary mRNA abundance of beta-defensin 5, toll-like-receptor 2 (TLR2), and TLR4 but not TLR9 in cattle. Clin Diagn Lab Immunol 11 (2004) 174-185
8. Wright S.D., Ramos R.A., Tobias P.S., Ulevitch R.J., and Mathison J.C. CD14, a receptor for complexes of lipopolysaccharide (LPS) and LPS binding protein. Science 21 (1990) 1431-1433
9. van Miert A.S.J.P.A.M. Acute phase response and non cellular defence mechanisms. Flem Vet J 62 (1991) 69-91
10. Otterlei M., Sundan A., Skjak-Braek G., Ryan L., Smidsrod O., and Espevik T. Similar mechanisms of action of defined polysaccharides and lipopolysaccharides: characterization of binding and tumor necrosis factor-α induction. Infect Immunity 61 (1993) 1917-1925
11. Paape M.J., Lilius E.M., Wiitanen P.A., Kontio M.P., and Miller R.H. Intramammary defense against infections induced by Escherichia coli in cows. Am J Vet Res 57 (1996) 477-482
12. Sladek Z., Rysanek D., and Faldyna M. Activation of phagocytes during initiation and resolution of mammary gland injury induced by lipopolysaccharide in heifers. Vet Res 33 (2002) 191-204
13. Schumann R.R., Leong S.R., Flaggs G.W., Gray P.W., Wright S.D., Mathison J.C., et al. Structure and function of lipopolysaccharide binding protein. Science 249 (1990) 1429-1431
14. Dentener M.A., Bazil V., Von Asmuth E.J., Ceska M., and Buurman W.A. Involvement of CD14 in lipopolysaccharide-induced tumor necrosis factor-alpha, IL-6 and IL-8 release by human monocytes and alveolar macrophages. J Immunol 150 (1993) 2885-2891
15. Martin T.R. Recognition of bacterial endotoxin in the lungs. Am J Respir Cell Mol Biol 23 (2000) 128-132
16. Guha M., and Mackman N. LPS induction of gene expression in human monocytes. Cell Signal 13 (2001) 85-94
17. Sladek Z., and Rysanek D. Neutrophil apoptosis during the resolution of bovine mammary gland injury. Res Vet Sci 70 (2001) 41-46
18. Savill J., and Fadok V. Corpse clearance defines the meaning of cell death. Nature 407 (2000) 784-788
19. Fadok V.A., Voelker D.R., Campbell P.A., Cohen J.J., Bratton D.L., and Henson P.M. Exposure of phosphatidylserine on the surface of apoptotic lymphocytes triggers specific recognition and removal by macrophages. J Immunol 148 (1992) 2207-2216
20. Devitt A., Pierce S., Oldreive C., Shingler W.H., and Gregory C.D. CD14-dependent clearance of apoptotic cells by human macrophages: the role of phosphatidylserine. Cell Death Differ 10 (2003) 371-382
21. Krahling S., Callahan M.K., Williamson P., and Schlegel R.A. Exposure of phosphatidylserine is a general feature in the phagocytosis of apoptotic lymphocytes by macrophages. Cell Death Differ 6 (1999) 183-189
22. Fox L.K., and Gay J.M. Contagious mastitis. Vet Clin North Am Food Anim Pract 9 (1993) 475-487
23. Pedersen L.H., Aalbaek B., Rontved C.M., Ingvartsen K.L., Sorensen N.S., Heegaard P.M., et al. Early pathogenesis and inflammatory response in experimental bovine mastitis due to Streptococcus uberis. J Comp Pathol 128 (2003) 156-164
24. Sladek Z., Rysanek D., Ryznarova H., and Faldyna M. Neutrophil apoptosis during experimentally induced Staphylococcus aureus mastitis. Vet Res 36 (2005) 629-643
25. Sladek Z, Rysanek D, Faldyna M, Ryznarova H. Neutrophils apoptosis during experimentally induced Streptococcus uberis mastitis. Vet Med Czech, submitted.
26. International Dairy Federation (IDF). Milk-enumeration of somatic cells. International IDF Standard 148A, 1995. 8pp.
27. Vermes I., Haanen C., Steffens-Nakken H., and Reutelingsperger C. A novel assay for apoptosis. Flow cytometric detection of phosphatidylserine expression on early apoptotic cells using fluorescein labelled Annexin V. J Immunol Methods 184 (1995) 39-51
28. Van Oostveldt K., Paape M.J., Dosogne H., and Burvenich C. Effect of apoptosis on phagocytosis, respiratory burst and CD18 adhesion receptor expression of bovine neutrophils. Domest Anim Endocrinol 22 (2002) 37-50
29. Henson P.M., Zanolari B., Schwartzman N.A., and Hong S.R. Intracellular control of human neutrophil secretion. I. C5a-induced stimulus-specific desensitization and the effects of cytochalasin B. J Immunol 121 (1978) 851-855
30. Riollet C., Rainard P., and Poutrel B. Differential induction of complement fragment C5a and inflammatory cytokines during intramammary infections with E. coli and Staphylococcus aureus. Clin Dian Lab Immunol 7 (2000) 161-167
31. Riollet C., Rainard P., and Poutrel B. Cell subpopulations and cytokine expression in cow milk in response to chronic Staphylococcus aureus infection. J Dairy Sci 84 (2001) 1077-1084
32. Bannerman D.D., Paape M.J., Lee J.W., Zhao X., Hope J.C., and Rainard P. E. coli and Staphylococcus aureus elicit differential innate immune responses following intramammary infection. Clin Diagn Lab Immunol 11 (2004) 463-472
33. Hill A.W. Pathogenicity of two strains of Streptococcus uberis infused into lactating and non-lactating bovine mammary glands. Res Vet Sci 45 (1988) 400-404
34. Hill A.W., Finch J.M., Field T.R., and Leigh J.A. Immune modification of the pathogenesis of Streptococcus uberis mastitis in the dairy cow. FEMS Immunol Med Microbiol 8 (1994) 109-117
35. 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
36. 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
37. Sladek Z., and Rysanek D. Apoptosis of polymorphonuclear leukocytes of the juvenile bovine mammary gland during induced influx. Vet Res 31 (2000) 553-563
38. Fournier B., and Philpott D.J. Recognition of Staphylococcus aureus by the innate immune system. Clin Microbiol Rev 18 (2005) 521-540
39. Moreillon P., and Majcherczyk P.A. Proinflammatory activity of cell-wall constituents from gram-positive bacteria. Scand J Infect Dis 35 (2003) 632-641
40. Boulanger D., Bureau F., Melotte D., Mainil J., and Lekeux P. Increased nuclear factor kappaB activity in milk cells of mastitis-affected cows. J Dairy Sci 86 (2003) 1259-1267
41. Kurt-Jones E.A., Mandell L., Whitney C., Padgett A., Gosselin K., Newburger P.E., et al. Role of toll-like receptor 2 (TLR2) in neutrophil activation: GM-CSF enhances TLR2 expression and TLR2-mediated interleukin 8 responses in neutrophils. Blood 100 (2002) 1860-1868
42. Wardley R.C., Rouse B.T., and Babiuk L.A. The mammary gland of the ox: a convenient source for the repeated collection of neutrophils and macrophages. J Reticuloendothel Soc 19 (1976) 29-36
43. Wang J.E., Jorgensen P.F., Ellingsen E.A., Almiof M., Thiemermann C., Foster S.J., et al. Peptidoglycan primes for LPS-induced release of proinflammatory cytokines in whole human blood. Shock 16 (2001) 178-182
44. Takada H., Yokoyama S., and Yang S. Enhancement of endotoxin activity by muramyldipeptide. J Endotoxin Res 8 (2002) 337-342
45. Maus U., Herold S., Muth H., Maus R., Ermert L., Ermert M., et al. Monocytes recruited into the alveolar air space of mice show a monocytic phenotype but upregulate CD14. Am J Physiol Lung Cell Mol 280 (2001) 58-68
46. Mullan N.A., Carter E.A., and Nguyen K.A. Phagocytic and bactericidal properties of bovine macrophages from non-lactating mammary glands. Res Vet Sci 38 (1985) 160-166
47. Lin S.M., Frevert C.W., Kajikawa O., Wurfel M.M., Ballman K., Mongovin S., et al. Differential regulation of membrane CD14 expression and endotoxin-tolerance in alveolar macrophages. Am J Respir Cell Mol Biol 31 (2004) 162-170
48. Prgomet C., Sarikaya H., Bruckmaier R.M., and Pfaffl M.W. Short-term effects on pro-inflammatory cytokine, lactoferrin and CD14 mRNA expression levels in bovine immunoseparated milk and blood cells treated by LPS. J Vet Med A Physiol Pathol Clin Med 52 (2005) 317-324
49. Dobrovolskaia M.A., and Vogel S.N. Toll receptors, CD14, and macrophage activation and deactivation by LPS. Microb. Infect 4 (2002) 903-914
50. Jiang J.X., Chen Y.H., Xie G.Q., Ji S.H., Liu D.W., Qiu J., et al. Intrapulmonary expression of scavenger receptor and CD14 and their relation to local inflammatory responses to endotoxemia in mice. World J Surg 27 (2003) 1-9
51. Karlsson H., Larsson P., Wold A.E., and Rudin A. Pattern of cytokine responses to gram-positive and gram-negative commensal bacteria is profoundly changed when monocytes differentiate into dendritic cells. Infect Immun 72 (2004) 2671-2678
52. Sugawara S., Nemoto E., Tada H., Miyake K., Imamura T., and Takada H. Proteolysis of human monocyte CD14 by cysteine proteinases (gingipains) from Porphyromonas gingivalis leading to lipopolysaccharide hyporesponsiveness. J Immunol 165 (2000) 411-418
53. Tapping R.I., and Tobias P.S. Cellular binding of soluble CD14 requires lipopolysaccharide (LPS) and LPS-binding protein. J Biol Chem 272 (1997) 23157-23164
54. Vangroenweghe F., Rainard P., Paape M., Duchateau L., and Burvenich C. Increase of E. coli inoculum doses induces faster innate immune response in primiparous cows. J Dairy Sci 87 (2004) 4132-4144
55. Bannerman D.D., Paape M.J., Hare W.R., and Sohn E.J. Increased levels of LPS-binding protein in bovine blood and milk following bacterial lipopolysaccharide challenge. J Dairy Sci 86 (2003) 3128-3137
56. Devitt A., Moffatt O.D., Raykundalia C., Capra J.D., Simmons D.L., and Gregory C.D. Human CD14 mediates recognition and phagocytosis of apoptotic cells. Nature 392 (1998) 505