Nontypeable Haemophilus influenzae is now established as an important human pathogen. It is the second leading cause of middle ear infections in children after the pneumococcus. Middle ear infection is an important health problem for children. Recurrent ear infections are associated with hearing loss, problems in speech and language development, and learning disabilities. Nontypeable H. influenzae is an important pathogen in several other settings as well, including sinusitis, lower respiratory tract infections, and neonatal sepsis. In view of the importance of this organism as a human pathogen, work proposed in this application will be directed toward understanding the pathogenesis and epidemiology of infection with a goal toward identifying potential vaccine antigens. In this proposal, we plan to continue our studies on the outer membrane proteins (OMPs) of nontypeable H. influenzae. The proposed studies will approach two major areas. In the first part (Specific Aims 1 and 2) work will focus on a common antigen among strains of the bacterium. This will involve antigenic and molecular studies of protein P6, a 16,600 dalton OMP. P6 is an important antigen in the human immune response to infection and possesses many characteristics to indicate that it is a promising vaccine candidate. Therefore, detailed antigenic and molecular studies of the P6 molecule are planned to understand its function as a potential virulence factor and potential vaccine antigen. The second major approach will focus on antigenic differences among strains of nontypeable H. influenzae. This work will involve the P2 OMP, an important surface antigen that is antigenically heterogeneous among strains. The goals of this work are to characterize the molecular basis of the antigenic differences and to raise monoclonal antibodies to determinants on P2 for the purpose of developing a serotyping system. A serotyping system for nontypeable H. influenzae will contribute importantly to an understanding of the pathogenesis and epidemiology of infection by this important human pathogen.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI019641-10
Application #
3128987
Study Section
Bacteriology and Mycology Subcommittee 2 (BM)
Project Start
1983-09-30
Project End
1995-07-31
Budget Start
1992-09-01
Budget End
1993-07-31
Support Year
10
Fiscal Year
1992
Total Cost
Indirect Cost
Name
State University of New York at Buffalo
Department
Type
Schools of Medicine
DUNS #
038633251
City
Buffalo
State
NY
Country
United States
Zip Code
14260
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Jacobs, David M; Ochs-Balcom, Heather M; Zhao, Jiwei et al. (2018) Lower Airway Bacterial Colonization Patterns and Species-Specific Interactions in Chronic Obstructive Pulmonary Disease. J Clin Microbiol 56:
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Gallo, Mary C; Kirkham, Charmaine; Eng, Samantha et al. (2018) Changes in IgA Protease Expression Are Conferred by Changes in Genomes during Persistent Infection by Nontypeable Haemophilus influenzae in Chronic Obstructive Pulmonary Disease. Infect Immun 86:
Otsuka, Taketo; Brauer, Aimee L; Kirkham, Charmaine et al. (2017) Antimicrobial activity of antisense peptide-peptide nucleic acid conjugates against non-typeable Haemophilus influenzae in planktonic and biofilm forms. J Antimicrob Chemother 72:137-144
Ahearn, Christian P; Gallo, Mary C; Murphy, Timothy F (2017) Insights on persistent airway infection by non-typeable Haemophilus influenzae in chronic obstructive pulmonary disease. Pathog Dis 75:
Pettigrew, Melinda M; Alderson, Mark R; Bakaletz, Lauren O et al. (2017) Panel 6: Vaccines. Otolaryngol Head Neck Surg 156:S76-S87
Murphy, Timothy F; Kirkham, Charmaine; Gallo, Mary C et al. (2017) Immunoglobulin A Protease Variants Facilitate Intracellular Survival in Epithelial Cells By Nontypeable Haemophilus influenzae That Persist in the Human Respiratory Tract in Chronic Obstructive Pulmonary Disease. J Infect Dis 216:1295-1302
Post, Deborah M B; Ketterer, Margaret R; Coffin, Jeremy E et al. (2016) Comparative Analyses of the Lipooligosaccharides from Nontypeable Haemophilus influenzae and Haemophilus haemolyticus Show Differences in Sialic Acid and Phosphorylcholine Modifications. Infect Immun 84:765-74
Hu, Fang; Rishishwar, Lavanya; Sivadas, Ambily et al. (2016) Comparative Genomic Analysis of Haemophilus haemolyticus and Nontypeable Haemophilus influenzae and a New Testing Scheme for Their Discrimination. J Clin Microbiol 54:3010-3017

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