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Selected Publication:

Häussler, S; Tümmler, B; Weissbrodt, H; Rohde, M; Steinmetz, I.
Small-colony variants of Pseudomonas aeruginosa in cystic fibrosis.
Clin Infect Dis. 1999; 29(3):621-625 Doi: 10.1086/598644 [OPEN ACCESS]
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Leading authors Med Uni Graz
Steinmetz Ivo
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Abstract:
In the context of chronic lung infection due to Pseudomonas aeruginosa in cystic fibrosis (CF), attention has been focused on the presence of the most common mucoid phenotype. In this study, the presence of small-colony variants (SCVs) of P. aeruginosa in respiratory tract specimens from patients with CF was investigated, and the clinical conditions predisposing to SCVs were analyzed. P. aeruginosa SCVs were isolated from 33 of 86 P. aeruginosa-positive CF patients over a 2-year period. Fast-growing revertants with larger surface colonies could be isolated from SCV populations. Electron microscopy revealed no significant difference in cell size or morphology. MICs of a broad range of antipseudomonas agents for SCVs were two- to eightfold higher than values for revertants. Recovery of SCVs was correlated with parameters revealing poor lung function and was significantly associated with daily inhalation of tobramycin or colistin.
Find related publications in this database (using NLM MeSH Indexing)
Adolescent -
Adult -
Anti-Bacterial Agents - pharmacology
Anti-Bacterial Agents - therapeutic use
Colony Count, Microbial -
Comorbidity -
Cystic Fibrosis - epidemiology
Female -
Female - epidemiology
Humans -
Male -
Microbial Sensitivity Tests -
Middle Aged -
Multivariate Analysis -
Pseudomonas Infections - drug therapy
Pseudomonas Infections - epidemiology
Pseudomonas Infections - microbiology
Pseudomonas aeruginosa - classification
Pseudomonas aeruginosa - drug effects
Retrospective Studies -
Sensitivity and Specificity -
Sputum - microbiology
Statistics, Nonparametric -

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