Background: Respiratory infections are well known triggers of asthma exacerbations, but their role in stable adult asthma remains unclear. Methods: 103 asthmatics and 30 control subjects were enrolled in the study. Sputum was induced by inhalation of 3% NaCl solution. Oropharyngeal swab specimens were obtained from the posterior wall of the oropharynx. Respiratory specimens were analysed by RT-PCR for rhinovirus, enterovirus and respiratory syncytial virus and by PCR for adenovirus, Chlamydia pneumoniae, Mycoplasma pneumoniae and Bordetella pertussis. Results: Sputum samples from two of the 30 healthy controls (6.7%), five of 53 patients with mild asthma (9.4%), and eight of 50 with moderate asthma (16.0%) were positive for rhinovirus. Rhinovirus positive asthmatic subjects had more asthma symptoms and lower forced expiratory volume in 1 second (FEV1) (79% predicted) than rhinovirus negative cases (93.5% predicted; p = 0.020). Chlamydia pneumoniae PCR was positive in 11 healthy controls (36.6%), 11 mild asthmatics (20.8%), and 11 moderate asthmatics (22%), and PCR positive asthmatics had lower FEV1/FVC than negative cases (78.2% v 80.8%, p = 0.023). Bordetella pertussis PCR was positive in 30 cases: five healthy controls (16.7%), 15 mild asthmatics (28.3%), and 10 moderate asthmatics (20%). Bordetella pertussis positive individuals had lower FEV1/FVC (77.1% v 80.7%, p = 0.012) and more asthma symptoms than B pertussis negative cases. Conclusions: Rhinovirus, C pneumoniae, and B pertussis are found in the sputum or pharyngeal swab specimens of asthmatic subjects without concurrent symptoms of infection or asthma exacerbation, as well as in some healthy controls. Positivity is associated with lower lung function and more frequent asthma symptoms.
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Mayo Clin, Dept Internal Med, Div Allergy, Asthma,Clin Immunol, Barron, WI USAMayo Clin, Dept Internal Med, Div Allergy, Asthma,Clin Immunol, Barron, WI USA
Rank, M. A.
Ochkur, S. I.
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Mayo Clin, Dept Biochem & Mol Biol, Div Pulm Med, Barron, WI USAMayo Clin, Dept Internal Med, Div Allergy, Asthma,Clin Immunol, Barron, WI USA
Ochkur, S. I.
Lewis, J. C.
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Mayo Clin, Dept Internal Med, Div Allergy, Asthma,Clin Immunol, Barron, WI USAMayo Clin, Dept Internal Med, Div Allergy, Asthma,Clin Immunol, Barron, WI USA
Lewis, J. C.
Teaford, H. G., III
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Mayo Clin, Dept Internal Med, Div Allergy, Asthma,Clin Immunol, Barron, WI USAMayo Clin, Dept Internal Med, Div Allergy, Asthma,Clin Immunol, Barron, WI USA
Teaford, H. G., III
Wesselius, L. J.
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Mayo Clin, Dept Biochem & Mol Biol, Div Pulm Med, Barron, WI USAMayo Clin, Dept Internal Med, Div Allergy, Asthma,Clin Immunol, Barron, WI USA
Wesselius, L. J.
Helmers, R. A.
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Mayo Clin, Dept Crit Care, Div Pulm Med, Barron, WI USAMayo Clin, Dept Internal Med, Div Allergy, Asthma,Clin Immunol, Barron, WI USA
Helmers, R. A.
Lee, N. A.
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Mayo Clin, Dept Biochem & Mol Biol, Div Hematol & Oncol, Barron, WI USAMayo Clin, Dept Internal Med, Div Allergy, Asthma,Clin Immunol, Barron, WI USA
Lee, N. A.
Nair, P.
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St Josephs Healthcare, Dept Med, Hamilton, ON, Canada
McMaster Univ, Hamilton, ON, CanadaMayo Clin, Dept Internal Med, Div Allergy, Asthma,Clin Immunol, Barron, WI USA
Nair, P.
Lee, J. J.
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Mayo Clin, Dept Internal Med, Div Allergy, Asthma,Clin Immunol, Barron, WI USA
Mayo Clin, Dept Biochem & Mol Biol, Div Pulm Med, Barron, WI USAMayo Clin, Dept Internal Med, Div Allergy, Asthma,Clin Immunol, Barron, WI USA