A striking feature of the biology of Haemophilus influenzae is that these organisms can be distinguished from nearly all other facultative, gram-negative bacteria by their absolute requirement for heme. Surprisingly little attention has been paid to understanding how this parasite satisfies this unusual nutritional requirement, especially while growing in its human host. This research project involves a comprehensive approach to this unexplored aspect of H. influenzae molecular biology and disease pathogenesis. The ultimate objective of this research program is the elucidation of the mechanisms used by both typable and nontypable strains of H. influenzae for the acquisition of heme, with particular emphasis on how this pathogen obtains heme from the serum proteins hemopexin and haptoglobin which bind heme and hemoglobin, respectively, in the human body. 1) The newly identified 100kd protein of H. influenzae type b, which binds heme:hemopexin complexes and has been shown to be necessary for utilization of heme bound to hemopexin, will be investigated for its structure-function relationships. In addition, the relationship of this macromolecule to the RTX family of cytotoxins will be determined. 2) The 51kd heme-binding lipoprotein, which is ubiquitous among H. influenzae strains, will be investigated to determine its involvement in transport of heme into the H. influenzae cell. Additional experiments will be performed to determine whether this unusual lipoprotein is a one component of a permease system related to the superfamily of periplasmic binding protein-dependent, ATP-linked transporters. 3) Other H. influenzae cell surface constituents involved in the acquisition of heme from carrier proteins will be identified by the use of molecular genetic techniques, with special emphasis on the nontypable H. influenzae proteins involved in this process. 4) The surface-exposed proteins of nontypable H. influenzae shown to be involved in the acquisition of heme will be evaluated for their potential for vaccine development. This last set of experiments is especially relevant in view of the lack of a vaccine to prevent both upper and lower respiratory tract disease caused by nontypable H. influenzae.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI017621-15
Application #
2060538
Study Section
Bacteriology and Mycology Subcommittee 2 (BM)
Project Start
1980-12-01
Project End
1997-11-30
Budget Start
1994-12-01
Budget End
1995-11-30
Support Year
15
Fiscal Year
1995
Total Cost
Indirect Cost
Name
University of Texas Sw Medical Center Dallas
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
City
Dallas
State
TX
Country
United States
Zip Code
75390
Blick, Robert J; Revel, Andrew T; Hansen, Eric J (2003) FindGDPs: identification of primers for labeling microbial transcriptomes for DNA microarray analysis. Bioinformatics 19:1718-9
Fink, D L; Cope, L D; Hansen, E J et al. (2001) The Hemophilus influenzae Hap autotransporter is a chymotrypsin clan serine protease and undergoes autoproteolysis via an intermolecular mechanism. J Biol Chem 276:39492-500
Cope, L D; Love, R P; Guinn, S E et al. (2001) Involvement of HxuC outer membrane protein in utilization of hemoglobin by Haemophilus influenzae. Infect Immun 69:2353-63
Cope, L D; Hrkal, Z; Hansen, E J (2000) Detection of phase variation in expression of proteins involved in hemoglobin and hemoglobin-haptoglobin binding by nontypeable Haemophilus influenzae. Infect Immun 68:4092-101
Cope, L D; Thomas, S E; Hrkal, Z et al. (1998) Binding of heme-hemopexin complexes by soluble HxuA protein allows utilization of this complexed heme by Haemophilus influenzae. Infect Immun 66:4511-6
Maciver, I; Latimer, J L; Liem, H H et al. (1996) Identification of an outer membrane protein involved in utilization of hemoglobin-haptoglobin complexes by nontypeable Haemophilus influenzae. Infect Immun 64:3703-12
Maciver, I; Hansen, E J (1996) Lack of expression of the global regulator OxyR in Haemophilus influenzae has a profound effect on growth phenotype. Infect Immun 64:4618-29
Cope, L D; Yogev, R; Muller-Eberhard, U et al. (1995) A gene cluster involved in the utilization of both free heme and heme:hemopexin by Haemophilus influenzae type b. J Bacteriol 177:2644-53
Jarosik, G P; Maciver, I; Hansen, E J (1995) Utilization of transferrin-bound iron by Haemophilus influenzae requires an intact tonB gene. Infect Immun 63:710-3
Jarosik, G P; Sanders, J D; Cope, L D et al. (1994) A functional tonB gene is required for both utilization of heme and virulence expression by Haemophilus influenzae type b. Infect Immun 62:2470-7

Showing the most recent 10 out of 33 publications