Vaccination of dairy cows with recombinant Streptococcus uberis adhesion molecule induces antibodies that reduce adherence to and internalization of S. uberis into bovine mammary epithelial cells

Veterinary Immunology and Immunopathology

Volumn 141, Issue 3-4, 2011, Pages 201-208

  Prado, M E ^a   Almeida, R A ^a   Ozen, C ^a   Luther, D A ^a   Lewis, M J ^a   Headrick, S J ^a   Oliver, S P ^a  

^a UNIVERSITY OF TENNESSEE   (United States)

Author keywords

Bacterial adherence; Bovine mastitis; Streptococcus uberis; Streptococcus uberis adhesion molecule; SUAM

Indexed keywords

CELL ADHESION MOLECULE; PHOSPHATE BUFFERED SALINE; RECOMBINANT STREPTOCOCCUS UBERIS ADHESION MOLECULE; RECOMBINANT VACCINE; UNCLASSIFIED DRUG;

ANIMAL CELL; ANTIBODY RESPONSE; ARTICLE; BREAST EPITHELIUM; CELL ADHESION; COMPARATIVE STUDY; CONTROLLED STUDY; DAIRY CATTLE; ENZYME LINKED IMMUNOSORBENT ASSAY; IN VITRO STUDY; INTERNALIZATION; LACTATION; NONHUMAN; OPSONIZATION; STREPTOCOCCUS UBERIS; VACCINATION;

ANIMALS; ANTIBODIES, BACTERIAL; BACTERIAL ADHESION; BACTERIAL PROTEINS; BACTERIAL VACCINES; CATTLE; CELL ADHESION MOLECULES; COLOSTRUM; DAIRYING; EPITHELIAL CELLS; FEMALE; MAMMARY GLANDS, ANIMAL; MASTITIS, BOVINE; RECOMBINANT PROTEINS; SERUM; STREPTOCOCCUS; VACCINES, SYNTHETIC;

BACTERIA (MICROORGANISMS); BOS; BOVINAE; STREPTOCOCCUS UBERIS;

EID: 79955579549     PISSN: 01652427     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.vetimm.2011.02.023     Document Type: Article

References (30)

1. Almeida R.A., Fang W.H., Oliver S.P. Adherence and internalization of Streptococcus uberis to bovine mammary epithelial cells are mediated by host cell proteoglycans. FEMS Microbiol. Lett. 1999, 177:313-317.
2. Almeida R.A., Luther D.A., Kumar S.J., Calvinho L.F., Bronze M.S., Oliver S.P. Adherence of Streptococcus uberis to bovine mammary epithelial cells and to extracellular matrix proteins. J. Vet. Med. B 1996, 43:385-392.
3. Almeida R.A., Luther D.A., Park H.M., Oliver S.P. Identification, isolation, and partial characterization of a novel Streptococcus uberis adhesion molecule (SUAM). Vet. Microbiol. 2006, 115:183-191.
4. Almeida R.A., Oliver S.P. Antiphagocytic effect of the capsule of Streptococcus uberis. Zentralbl. Veterinarmed. B 1993, 40:707-714.
5. Almeida R.A., Oliver S.P. Role of collagen in adherence of Streptococcus uberis to bovine mammary epithelial cells. J. Vet. Med. B: Infect. Dis. Vet. Public Health 2001, 48:759-763.
6. Bradley A. Bovine mastitis: an evolving disease. Vet. J. 2002, 164:116-128.
7. Confer A.W., Ayalew S., Panciera R.J., Montelongo M., Wray J.H. Recombinant Mannheimia haemolytica serotype 1 outer membrane protein PlpE enhances commercial M-haemolytica vaccine-induced resistance against serotype 6 challenge. Vaccine 2006, 24:2248-2255.
8. Hogan J.S., Smith K.L., Hoblet K.H., Schoenberger P.S., Todhunter D.A., Hueston W.D., Pritchard D.E., Bowman G.L., Heider L.E., Brockett B.L., Conrad H.R. Field survey of clinical mastitis in low somatic-cell count herds. J. Dairy Sci. 1989, 72:1547-1556.
9. Huynh H.T., Robitaille G., Turner J.D. Establishment of bovine mammary epithelial cells (Mac-T) an in vitro model for bovine lactation. Exp. Cell Res. 1991, 197:191-199.
10. Jayarao B.M., Gillespie B.E., Lewis M.J., Dowlen H.H., Oliver S.P. Epidemiology of Streptococcus uberis intramammary infections in a dairy herd. J. Vet. Med. B 1999, 46:433-442.
11. Jayarao B.M., Oliver S.P., Tagg J.R., Matthews K.R. Genotypic and phenotypic analysis of Streptococcus uberis isolated from bovine mammary secretions. Epidemiol. Infect. 1991, 107:543-555.
12. Jiang M., Babiuk L.A., Potter A.A. Cloning, sequencing and expression of the CAMP factor gene of Streptococcus uberis. Microb. Pathogenesis 1996, 20:297-307.
13. Leigh J.A. Purification of a plasminogen activator from Streptococcus uberis. FEMS Microbiol. Lett. 1994, 118:153-158.
14. Lopes M.F., Merquior V.L., Peralta J.M., Teixeira L.M. Partial characterization of the cohemolytic factor produced by Streptococcus uberis and comparison with the CAMP-factor. FEMS Immunol. Med. Microbiol. 1995, 12:205-212.
15. Luther D.A., Almeida R.A., Oliver S.P. Elucidation of the DNA sequence of Streptococcus uberis adhesion molecule gene (sua) and detection of sua in strains of Streptococcus uberis isolated from geographically diverse locations. Vet. Microbiol. 2008, 128:304-312.
16. Luther D.A., Chen X., Almeida R.A., Yuan Y., Chang S., Eurife A., Jory L., Kovacevic S., Allen A., Oliver S.P. Detection of Streptococcus uberis adhesion molecule (SUAM) and sua in geographically diverse strains of S. uberis. International Dairy Federation Mastitis Conference 2010, 705.
17. Matthews K.R., Almeida R.A., Oliver S.P. Bovine mammary epithelial cell invasion by Streptococcus uberis. Infect. Immun. 1994, 62:5641-5646.
18. Oliver S.P. Frequency of isolation of environmental mastitis causing pathogens and incidence of new intramammary infection during the nonlactating period. Am. J. Vet. Res. 1988, 49:1789-1793.
19. Oliver S.P., Almeida R.A., Calvinho L.F. Virulence factors of Streptococcus uberis isolated from cows with mastitis. Zentralbl. Veterinarmed. B 1998, 45:461-471.
20. Oliver S.P., Almeida R.A., Gillespie B.E., Ivey S.J., Moorehead H., Lunn P., Dowlen H.H., Johnson D.L., Lamar K.C. Efficacy of extended pirlimycin therapy for treatment of experimentally induced Streptococcus uberis intramammary infections in lactating dairy cattle. Vet. Ther. 2003, 4:299-308.
21. Oliver S.P., Gillespie B.E., Headrick S.J., Lewis M.J., Dowlen H.H. Prevalence, risk factors, and strategies for controlling mastitis in heifers during the periparturient period. Intern. J. Appl. Res. Vet. Med. 2005, 3:150-162.
22. Oliver S.P., Gillespie B.E., Jayarao B.M. Detection of new and persistent Streptococcus uberis and Streptococcus dysgalactiae intramammary infections by polymerase chain reaction-based DNA fingerprinting. FEMS Microbiol. Lett. 1998, 160:69-73.
23. Oliver S.P., Mitchell B.A. Prevalence of mastitis pathogens in herds participating in a mastitis control program. J. Dairy Sci. 1984, 67:2436-2440.
24. Patel D., Almeida R.A., Dunlap J.R., Oliver S.P. Bovine lactoferrin serves as a molecular bridge for internalization of Streptococcus uberis into bovine mammary epithelial cells. Vet. Microbiol. 2009, 137:297-301.
25. Rosey E.L., Lincoln R.A., Ward P.N., Yancey R.J., Leigh J.A. PauA: a novel plasminogen activator from Streptococcus uberis. FEMS Microbiol. Lett. 1999, 178:27-33.
26. Schaufuss P., Sting R., Schaeg W., Blobel H. Isolation and characterization of hyaluronidase from Streptococcus uberis. Zentralbl. Bakteriol. 1989, 271:46-53.
27. Shapiro S.S., Wilk M.B. An analysis of variance test for normality (complete samples). Biometrika 1965, 52:591.
28. Smith K.L., Todhunter D.A., Schoenberger P.S. Environmental pathogens and intramammary infection during the dry period. J. Dairy Sci. 1985, 68:402-417.
29. Tamilselvam B., Almeida R.A., Dunlap J.R., Oliver S.P. Streptococcus uberis internalizes and persists in bovine mammary epithelial cells. Microb. Pathogenesis 2006, 40:279-285.
30. Zadoks R.N., Gillespie B.E., Barkema H.W., Sampimon O.C., Oliver S.P., Schukken Y.H. Clinical, epidemiological and molecular characteristics of Streptococcus uberis infections in dairy herds. Epidemiol. Infect. 2003, 130:335-349.