It is estimated that 4 million children die of severe lower respiratory tract disease per year in developing countries. Viruses probably cause the majority of lower respiratory tract disease, however, bacteria appear to be responsible for most of the severe mortality and morbidity. Although it has been difficult to establish the etiologic agents responsible for lower respiratory tract disease, the most common bacterial agents observed are Haemophilus influenzae and Streptococcus pneumoniae. Several studies have now documented that a substantial fraction of the H. influenzae isolates are nontypable. Granoff, Weinberg and co-workers have characterized Haemophilus isolates from the blood of patients with lower respiratory tract disease in Pakistan. Thirty-two percent of the 105 Haemophilus isolates they examined were nontypable. Isolates from patients with invasive disease in Papua New Guinea and the Philippines have also been examined by these workers. Fifteen percent of the isolates from the Papua New Guinea collection and 37% of the isolates from the Philippine collection were nontypable. Thus, the available data indicate that nontypable Haemophilus is an important cause of lower respiratory tract disease in children in the developing world. In the developed world, NTHI are an important cause of infections of mucosal surfaces such as otitis media, sinusitis and bronchitis. It is not clear at present whether or not the NTHI isolates from children in the developing world are different from the NTHI isolates in the developed world which are responsible for 1) mucosal surface infections in children, 2) pneumonia and other serious infections in immunocompromised patients, or 3) exacerbations of chronic bronchitis in adults. The overall goals of the proposed studies are 1) to characterize the nontypable influenzas strains which are responsible for severe lower respiratory tract disease in children in the developing world and 2) to develop strategies for creating new vaccines for children at risk for contracting severe lower respiratory disease caused by these organisms. These studies will also provide a foundation for developing vaccines for prevention of otitis media, sinusitis, and bronchitis 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 #
5R01AI017572-14
Application #
2060530
Study Section
Bacteriology and Mycology Subcommittee 2 (BM)
Project Start
1980-07-01
Project End
1994-10-31
Budget Start
1994-05-01
Budget End
1994-10-31
Support Year
14
Fiscal Year
1994
Total Cost
Indirect Cost
Name
Washington University
Department
Pediatrics
Type
Schools of Medicine
DUNS #
062761671
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Yang, Y P; Munson Jr, R S; Grass, S et al. (1997) Effect of lipid modification on the physicochemical, structural, antigenic and immunoprotective properties of Haemophilus influenzae outer membrane protein P6. Vaccine 15:976-87
Bell, J; Grass, S; Jeanteur, D et al. (1994) Diversity of the P2 protein among nontypeable Haemophilus influenzae isolates. Infect Immun 62:2639-43
Munson Jr, R S; Sasaki, K (1993) Protein D, a putative immunoglobulin D-binding protein produced by Haemophilus influenzae, is glycerophosphodiester phosphodiesterase. J Bacteriol 175:4569-71
Munson Jr, R S; Grass, S; West, R (1993) Molecular cloning and sequence of the gene for outer membrane protein P5 of Haemophilus influenzae. Infect Immun 61:4017-20
Munson Jr, R; Brodeur, B; Chong, P et al. (1992) Outer membrane proteins P1 and P2 of Haemophilus influenzae type b: structure and identification of surface-exposed epitopes. J Infect Dis 165 Suppl 1:S86-9
Coleman, T; Grass, S; Munson Jr, R (1991) Molecular cloning, expression, and sequence of the pilin gene from nontypeable Haemophilus influenzae M37. Infect Immun 59:1716-22
Munson Jr, R; Grass, S; Bailey, C (1991) Comparison of the structure of the genes for outer membrane proteins P1 and P2 of Haemophilus influenzae type b. Mol Immunol 28:257-9
Nelson, M B; Munson Jr, R S; Apicella, M A et al. (1991) Molecular conservation of the P6 outer membrane protein among strains of Haemophilus influenzae: analysis of antigenic determinants, gene sequences, and restriction fragment length polymorphisms. Infect Immun 59:2658-63
Martin, D; Munson Jr, R; Grass, S et al. (1991) Mapping of B-cell epitopes on the outer membrane P2 porin protein of Haemophilus influenzae by using recombinant proteins and synthetic peptides. Infect Immun 59:1457-64
Proulx, C; Munson Jr, R S; Grass, S et al. (1991) Identification of a surface-exposed immunodominant epitope on outer membrane protein P1 of Haemophilus influenzae type b. Infect Immun 59:963-70

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