Use of 16S rRNA Gene Profiling by Terminal Restriction Fragment Length Polymorphism Analysis To Compare Bacterial Communities in Sputum and Mouthwash Samples from Patients with Cystic Fibrosis
Open Access
- 1 July 2006
- journal article
- research article
- Published by American Society for Microbiology in Journal of Clinical Microbiology
- Vol. 44 (7), 2601-2604
- https://doi.org/10.1128/jcm.02282-05
Abstract
The bacterial communities present in the oral cavity and the lungs of 19 adult cystic fibrosis (CF) patients were compared by using terminal restriction fragment length polymorphism analysis of 16S rRNA gene PCR products amplified from nucleic acids extracted directly from bacteria in clinical samples. Sputum samples were not found to be subject to profound contamination by oral cavity bacteria. Evidence of colonization of the CF lung by certain oral bacterial species was found.Keywords
This publication has 10 references indexed in Scilit:
- Bacterial activity in cystic fibrosis lung infectionsRespiratory Research, 2005
- Characterization of Bacterial Community Diversity in Cystic Fibrosis Lung Infections by Use of 16S Ribosomal DNA Terminal Restriction Fragment Length Polymorphism ProfilingJournal of Clinical Microbiology, 2004
- Bacterial Diversity in Cases of Lung Infection in Cystic Fibrosis Patients: 16S Ribosomal DNA (rDNA) Length Heterogeneity PCR and 16S rDNA Terminal Restriction Fragment Length Polymorphism ProfilingJournal of Clinical Microbiology, 2003
- Application of terminal RFLP analysis to characterize oral bacterial flora in saliva of healthy subjects and patients with periodontitisJournal of Medical Microbiology, 2003
- Oral health and respiratory infection.2002
- Bacterial Diversity in Human Subgingival PlaqueJournal of Bacteriology, 2001
- Role of Oral Bacteria in Respiratory InfectionThe Journal of Periodontology, 1999
- Associations Between Oral Conditions and Respiratory Disease in a National Sample Survey PopulationAnnals of Periodontology, 1998
- Characterization of microbial diversity by determining terminal restriction fragment length polymorphisms of genes encoding 16S rRNAApplied and Environmental Microbiology, 1997