Haemophilus influenzae surface fibrils contribute to serum resistance by interacting with vitronectin

Journal of Immunology

Volumn 177, Issue 1, 2006, Pages 430-436

  Hallström, Teresia ^a   Trajkovska, Elena ^a   Forsgren, Arne ^a   Riesbeck, Kristian ^a  

^a LUND UNIVERSITY   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

BACTERIAL PROTEIN; COMPLEMENT MEMBRANE ATTACK COMPLEX; PROTEIN HSF; UNCLASSIFIED DRUG; VIRULENCE FACTOR; VITRONECTIN;

ARTICLE; BACTERIAL SURVIVAL; BACTERICIDAL ACTIVITY; BACTERIUM MUTANT; BINDING SITE; COMPLEMENT SYSTEM; CONTROLLED STUDY; ESCHERICHIA COLI; EXTRACELLULAR MATRIX; HAEMOPHILUS INFLUENZAE TYPE B; HUMAN; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN DOMAIN;

EID: 33745324685     PISSN: 00221767     EISSN: None     Source Type: Journal    
DOI: 10.4049/jimmunol.177.1.430     Document Type: Article

References (43)

1. Turk, D. C. 1984. The pathogenicity of Haemophilus influenzae. J. Med. Microbiol. 18: 1-16.
2. Jacobs, M. R., R. Dagan, P. C. Appelbaum, and D. J. Burch. 1998. Prevalence of antimicrobial-resistant pathogens in middle ear fluid: multinational study of 917 children with acute otitis media. Antimicrob. Agents Chemother. 42: 589-595.
3. Broome, C. V. 1987. Epidemiology of Haemophilus influenzae type b infections in the United States. Pediatr. Infect. Dis. J. 6: 779-782.
4. Murphy, T. F., J. M. Bernstein, D. M. Dryja, A. A. Campagnari, and M. A. Apicella. 1987. Outer membrane protein and lipooligosaccharide analysis of paired nasopharyngeal and middle ear isolates in otitis media due to nontypeable Haemophilus influence: pathogenic and epidemiologic observations. J. Infect. Dis. 5: 960-962.
5. Read, R. C., R. Wilson, A. Rutman, V. Lund, H. C. Todd, A. P. Brain, P. K. Jeffery, and P. J. Cole. 1991. Interaction of nontypeable Haemophilus influenzas with human respiratory mucosa in vitro. J. Infect. Dis. 163: 549-558.
6. Wilson, R., R. Read, and P. Cole. 1992. Interaction of Haemophilus influenzae with mucus, cilia, and respiratory epithelium. J. Infect. Dis. 165: 100-102.
7. St. Geme, J. W., III, M. L. De la Morena, and S. Falkow. 1994. A Haemophilus influenzae IgA protease-like protein promotes intimate interaction with human epithelial cells. Mol. Microbiol. 14: 217-233.
8. Fink, D. L., B. A. Green, and J. W. St. Geme, III. 2002. The Haemophilus influenzae Hap autotransporter binds to fibronectin, laminin, and collagen IV. Infect. Immun. 70: 4902-4907.
9. Eberhard, T., and M. Ullberg. 2002. Interaction of vitronectin with Haemophilus influenzae. FEMS Immun. Med. Microbiol. 34: 215-219.
10. Hultgren, S. J., S. Abraham, M. Caparon, P. Falk, J. W. St. Geme, III, and S. Normark. 1993. Pilus and nonpilus bacterial adhesins: assembly and function in cell recognition. Cell 73: 887-901.
11. Stall, T. L., P. M. Mendelman, J. E. Haas, M. A. Schoenborn, K. D. Mack, and A. L. Smith. 1984. Characterization of Haemophilus influenzae type b fimbriae. Infect. Immun. 46: 787-796.
12. Virkola, R., M. Brummer, H. Rauvala, L. van Alphen, and T. K. Korhonen. 2002. Interaction of fimbriae of Haemophilus influenzae with heparin-binding extracellular matrix proteins. J. Infect. Dis. 173: 1137-1147.
13. Ecevit, I. Z., K. W. McCrea, M. M. Pettigrew, A. Sen, C. F. Marrs, and J. R. Gilsdorf. 2004. Prevalence of the HifBC, hmw1A, hmw2A, hmwC, and hia genes in Haemophilus influenzae isolates. J. Clin. Microbiol 42: 3065-3072.
14. Barenkamp, S. J., and E. Leininger. 1992. Cloning, expression, and DNA sequence analysis of genes encoding nontypeable Haemophilus influenzae high-molecular-weight surface-exposed proteins related to filamentous hemagglutinin of Bordetella pertussis. Infect. Immun. 60: 1302-1313.
15. St. Geme, J. W., III, S. Falkow, and S. J. Barenkamp. 1993. High-molecular-weight proteins of nontypable Haemophilus influenzae mediate attachment to human epithelial cells. Proc. Natl. Acad. Sci. USA 90: 2875-2879.
16. Barenkamp, S. J., and J. W. St. Geme, III. 1996. Identification of a second family of high-molecular-weight adhesion proteins expressed by nontypeable Haemophilus influenzae. Mol. Microbiol. 19: 1215-1223.
17. St. Geme, J. W., III, D. Cutter, and S. J. Barenkamp. 1996. Characterization of the genetic locus encoding Haemophilus influenzae type b surface fibrils. J. Bacteriol. 69: 695-705.
18. St. Geme, J. W., III, and D. Cutter. 2000. The Haemophilus influenzae Hia adhesin is an autotransporter protein that remains uncleaved at the C terminus and fully cell associated. J. Bacteriol. 182: 6005-6013.
19. Laarmann, S., D. Cutter, T. Juehne, S. J. Barenkamp, and J. W. St. Geme, III. 2002. The Haemophilus influenzae Hia autotransporter harbors two adhesive pockets that reside in the passenger domain and recognize the same host cell receptor. Mol. Microbiol. 46: 731-743.
20. Schvartz, I., D. Seger, and S. Shaltiel. 1999. Vitronectin. Int. J. Biochem. Cell Biol. 31: 539-534.
21. Kroll, J. S., and R. Moxon. 1988. Capsulation and gene copy number at the cap locus of Haemophilus influenzae type b. J. Bacteriol. 170: 859-864.
22. Musset, J. M., J. S. Kroll, D. M. Granoff, E. R. Moxon, B. R. Brodeur, J. Campos, H. Dapernet, W. Fredriksen, J. Hanel, G. Hammond, et al. 1990. Global genetic structure and molecular epidemiology of encapsulated Haemophilus influenzae. Rev. Infect. Dis. 12: 75-111.
23. Poje, G., and J. R. Redfield. 2003. Transformation of Haemophilus influenzas. Methods Mol. Med. 71: 57-70.
24. Möllenkvist, A., T. Nordström, C. Halldén, J. J. Christensen, A. Forsgren, and K. Riesbeck. 2003. The Moraxella catarrhalis immunoglobulin D-binding protein MID has conserved sequences and is regulated by a mechanism corresponding to phase variation: the Moraxella catarrhalis immunoglobulin D-binding protein MID has conserved sequences and is regulated by a mechanism corresponding to phase variation. J. Bacteriol. 185: 2285-2295.
25. Laemmli, U. K. 1970. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227: 680-685.
26. Nordström, T., A. M. Blom, T. T. Tan, A. Forsgren, and K. Riesbeck. 2005. Ionic binding of C3 to the human pathogen Moraxella catarrhalis is unique mechanism for combating innate immunity. J. Immunol. 175: 3628-3636.
27. 131I-labeled human growth hormone of high specific radioactivity. Biochem. J. 89: 114-123.
28. Liang, O. D., S. Rosenblatt, G. S. Chhatwal, and K. T. Preissner. 1997. Identification of novel heparin-binding domains of vitronectin. FEBS Lett. 407: 169-172.
29. Chhatwal, G. S., K. T. Preissner, G. Müller-Berghaus, and H. Blobel. 1987. Specific binding of the human S protein (vitronectin) to streptococci, Staphylococcus aureus, and Esherichia coli. Infect. Immun. 55: 1878-1883.
30. Blom, A. M., A. Rytkonen, P. Vasquez, G. Lindahl, B. Dahlbäck, and A. B. Jonsson. 2001. A novel interaction between type IV pili of Neisseria gonorrhoeae and the human complement regulator C4B-binding protein. J. Immunol. 166: 6764-6770.
31. Lindahl, G., U. Sjöbring, and E. Johnsson. 2000. Human complement regulators; a major target for pathogenic microorganisms. Curr. Opin. Immunol. 12: 44-51.
32. Nordström, T., A. M. Blom, A. Forsgren, and K. Riesbeck. 2004. The emerging pathogen Moraxella catarrhalis interacts with complement inhibitor C4b binding protein through ubiquitous surface proteins Al and A2. J. Immunol. 173: 4598-4606.
33. Persson, C., I. Erjefalt, U. Alkner, C. Baumgarten, L. Greiff, B. Gustavsson, A. Luts, U. Pipkorn, F. Sundler, L. Svensson, et al. 1991. Plasma exudation as a first line respiratory mucosal defense. Clin. Exp. Allergy 21: 17-24.
34. Greiff, D., I. Erjefalt, C. Svensson, P. Wollmer, U. Alkner, M. Andersson, and C. G. Persson. 1993. Plasma exudation and solute absorption across airway mucosa. Clin. Physiol. 13: 219-233.
35. Rauterberg, E. W. 1998. The Complement Sysiem. K. Rother and G. O. Till, eds. Springer Verlag, Berlin, p. 287.
36. Hussain, M., K. Becker, C. Von Eiff, J. Schrenzel, G. Peters, and M. Herrmann. 2001. Identification and characterization of a novel 38.5-kilodalton cell surface protein of Staphylococcus aureus with extended-spectrum binding activity for extracellular matrix and plasma proteins. J. Bacteriol. 183: 6778-6786.
37. Podack, E. R., and H. J. Müller-Eberhard. 1979. Isolation of human S-protein, an inhibitor of the membrane attack complex of complement. J. Biol. Chem. 254: 9908-9914.
38. Preissner, K. T. 1991. Structure and biological role of vitronectin. Annu. Rev. Cell Biol 7: 275-310.
39. Pilz, D., T. Vocke, J. Heesemann, and V. Brade. 1992. Mechanism of YadA-mediated serum resistance of Yersinia enterocolitica serotype 03. Infect. Immun. 60: 189-195.
40. Cotter, S. E., H. Yeo, T. Juehne, and J. W. St. Geme, III. 2005. Architecture and adhesive activity of the Haemophilus influence Hsf adhesin. J. Bacteriol. 187: 4656-4664.
41. v integrin receptors. FEBS Lett. 424: 84-88.
42. 3 and v5 integrin-like vitronectin (VN) receptors in Candida albicans and their involvement in yeast cell adhesion to VN. J. Infect. Dis. 180: 156-166.
43. Limper, A. H., J. E. Standing, O. A. Hoffman, M. Castro, and L. W. Neese. 1993. Vitronectin binds to Pneumocystis carinii and mediates organism attachment to cultured lung epithelial cells. Infect. Immun. 61: 4302-439.