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Visualization of Pseudomonas aeruginosa within the Sputum of Cystic Fibrosis Patients
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First isolations of Segniliparus rugosus from patients with cystic fibrosis

W Ray Butler1, Catherine A Sheils, Barbara A Brown-Elliott

  • 1Centers for Disease Control and Prevention, Division of Tuberculosis Elimination, 1600 Clifton Rd., NE, M/S F08, Atlanta, GA 30333, USA. wrb1@cdc.gov

Journal of Clinical Microbiology
|August 3, 2007
PubMed

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Cystic fibrosis (CF), an autosomal recessive disorder, significantly affects the function of exocrine glands. This genetically inherited disease is characterized by the production of thick and sticky mucus, which can severely affect various organs and systems in the body.
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation, but...