The isolation and characterization of non-typeable Haemophilus influenzae from the sputum of adult cystic fibrosis patients.

The role of non-typeable Haemophilus influenzae in cystic fibrosis (CF) remains unclear. We wanted, therefore, to determine the presence and characteristics of non-typeable H. influenzae in sputum samples from patients with CF. In order to do this, we have assessed sputum samples from 55 consecutive clinically stable patients seen routinely at an adult CF out-patient clinic. Quantitative bacterial culture was performed using a selective media containing cefsoludin, and isolates were characterized by biotyping and outer membrane protein profile analysis. In 17 (30%) of these samples, non-typeable H. influenzae was isolated and was present in similar viable numbers (mean 7.7 x 10(8) colony-forming units (cfu).mL-1; SEM 3.1) to Pseudomonas aeruginosa (mean 8 x 10(8) cfu.mL-1: SEM 2.4). All non-typeable H. influenzae isolates recovered were beta-lactamase negative and sensitive to a range of antibiotics. Several biotypes and outer membrane protein profiles were observed, with no apparent association between these two phenotypic characteristics. The study showed that large numbers of non-typeable H. influenzae are often present in sputum from adult patients with CF. Further longitudinal studies of outer-membrane protein profile analysis are required to determine the dynamics of non-typeable H. influenzae colonization in individual patients and the clinical significance.

[1]  E. Myhre Typing of Haemophilus influenzae by counterimmunoelectrophoresis. , 2009, Acta pathologica et microbiologica Scandinavica. Section B: Microbiology and immunology.

[2]  N. Høiby Epidemiological investigations of the respiratory tract bacteriology in patients with cystic fibrosis. , 2009, Acta pathologica et microbiologica Scandinavica. Section B: Microbiology and immunology.

[3]  N. Høiby Pseudomonas aeruginosa infection in cystic fibrosis. Relationship between mucoid strains of Pseudomonas aeruginosa and the humoral immune response. , 2009 .

[4]  R. Stockley,et al.  Simple method for quantifying viable bacterial numbers in sputum. , 1995, Journal of clinical pathology.

[5]  N. Høiby,et al.  Pathogenesis of cystic fibrosis , 1993, The Lancet.

[6]  T. Murphy,et al.  Bacterial infection in chronic obstructive pulmonary disease. , 1992, The American review of respiratory disease.

[7]  D. Norman,et al.  In Vitro Tumor Necrosis Factor-α Secretion by Monocytes from Patients with Cystic Fibrosis , 1992 .

[8]  J. Sarwar,et al.  Strain-specific and immunodominant surface epitopes of the P2 porin protein of nontypeable Haemophilus influenzae , 1991, Infection and immunity.

[9]  R. Rayner,et al.  Haemophilus infection in cystic fibrosis. , 1990, Archives of disease in childhood.

[10]  G. Redding,et al.  Endobronchial Infection in Cystic Fibrosis , 1989, Acta paediatrica Scandinavica. Supplement.

[11]  L. van Alphen,et al.  Antigenic drift of Haemophilus influenzae in patients with chronic obstructive pulmonary disease , 1989, Infection and immunity.

[12]  R. Stockley,et al.  Activities and sources of beta-lactamase in sputum from patients with bronchiectasis , 1989, Journal of clinical microbiology.

[13]  T. Murphy,et al.  Human bactericidal antibody response to outer membrane protein P2 of nontypeable Haemophilus influenzae , 1988, Infection and immunity.

[14]  D. Geddes,et al.  Antimicrobial therapy against Staphylococcus aureus, Pseudomonas aeruginosa, and Pseudomonas cepacia. , 1988, Chest.

[15]  L. van Alphen,et al.  Changes in outer membrane proteins of nontypable Haemophilus influenzae in patients with chronic obstructive pulmonary disease. , 1988, The Journal of infectious diseases.

[16]  N. Høiby,et al.  Immunologic aspects of cystic fibrosis. , 1988, Chest.

[17]  K C Watson,et al.  Temporal changes in biotypes of Haemophilus influenzae isolated from patients with cystic fibrosis. , 1988, Journal of medical microbiology.

[18]  J. Govan,et al.  Pseudomonas aeruginosa and cystic fibrosis: unusual bacterial adaptation and pathogenesis. , 1986, Microbiological sciences.

[19]  M. Apicella,et al.  Antigenic heterogeneity of outer membrane proteins of nontypable Haemophilus influenzae is a basis for a serotyping system , 1985, Infection and immunity.

[20]  K. Watson,et al.  Distribution of biotypes of Haemophilus influenzae and H parainfluenzae in patients with cystic fibrosis. , 1985, Journal of clinical pathology.

[21]  N. HØiby,et al.  Antibiotic Treatment of Haemophilus Influenzae and Haemophilus Parainfluenzae Infections in Patients with Cystic Fibrosis , 1984, Acta paediatrica Scandinavica.

[22]  N. Høiby MICROBIOLOGY OF LUNG INFECTIONS IN CYSTIC FIBROSIS PATIENTS , 1982 .

[23]  P. Cole,et al.  USE OF SELECTIVE MEDIA IN BACTERIOLOGICAL INVESTIGATION OF PATIENTS WITH CHRONIC SUPPURATIVE RESPIRATORY INFECTION , 1980, The Lancet.

[24]  M. Kilian A taxonomic study of the genus Haemophilus, with the proposal of a new species. , 1976, Journal of general microbiology.

[25]  Oliver H. Lowry,et al.  Protein measurement with the Folin phenol reagent. , 1951, The Journal of biological chemistry.

[26]  J. Govan,et al.  Microbiology of lung infection in cystic fibrosis. , 1992, British medical bulletin.

[27]  S. Pedersen,et al.  Lung infection with alginate-producing, mucoid Pseudomonas aeruginosa in cystic fibrosis. , 1992, APMIS. Supplementum.

[28]  G. Hodges,et al.  Clinical significance of serotype, biotype, and beta-lactamase production of respiratory isolates of Hemophilus influenzae. , 1984, American journal of clinical pathology.

[29]  M. Hodson Cystic fibrosis in adolescents and adults. , 1983, The Practitioner.

[30]  J. Gustafson,et al.  Cystic Fibrosis , 2009, Journal of the Iowa Medical Society.