BackgroundMolecular diagnostics have led to the identification of a broad range of bacterial species in cystic fibrosis (CF) including
Inquilinus. The clinical significance of
Inquilinus in CF has not been thoroughly characterized.
MethodsRetrospective, case-control study of persons with CF from two CF centers with at least one respiratory culture positive for
Inquilinus spp
. compared with age-matched CF controls with chronic
Pseudomonas aeruginosa. Percent predicted forced expiratory volume in one second (ppFEV1) and body mass index percentile (BMI) were modeled from time of first positive culture up to 5 years later. Rates of pulmonary exacerbations were compared.
Inquilinus isolates were genotyped to evaluate strain diversity.
ResultsSeventeen patients with
Inquilinus infection were identified with a mean age of 13 years at first positive culture. Most cases had multiple cultures positive for
Inquilinus. ppFEV1 was not different between cases versus controls (80.2% vs 81.6%,
p = 0.97 at baseline, 67.5% vs. 73.3%,
p = 0.82 at 5 years). Patients were undernourished and BMI percentiles did not differ between groups (30.7% vs 43.4%,
p = 0.32 at baseline, 37.9% vs. 37.6%,
p = 0.98 at 5 years). There was no difference in the pulmonary exacerbation rate (3.0/year vs 2.5/year,
p = 0.34). Genotyping showed diverse genetic strains between patients.
ConclusionsInquilinus can present in childhood and is often associated with chronic infection in CF. Lung function and nutrition status at time of detection, lung function decline, and pulmonary exacerbation rates in
Inquilinus cases were similar to those with chronic
P. aeruginosa, a well-established CF pathogen.
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