Previous Article | Next Article 
Journal of Clinical Microbiology, November 2004, p. 5176-5183, Vol. 42, No. 11
0095-1137/04/$08.00+0 DOI: 10.1128/JCM.42.11.5176-5183.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.
Characterization of Bacterial Community Diversity in Cystic Fibrosis Lung Infections by Use of 16S Ribosomal DNA Terminal Restriction Fragment Length Polymorphism Profiling
G. B. Rogers,1,2
M. P. Carroll,2
D. J. Serisier,2
P. M. Hockey,2
G. Jones,3 and
K. D. Bruce1*
Division of Life Sciences, King's College London, London,1
Cystic Fibrosis Unit,2
The Public Health Laboratory Service, Southampton University Hospital, Southampton, United Kingdom3
Received 6 January 2004/
Returned for modification 4 April 2004/
Accepted 26 July 2004
Progressive loss of lung function resulting from the inflammatory response to bacterial colonization is the leading cause of mortality in cystic fibrosis (CF) patients. A greater understanding of these bacterial infections is needed to improve lung disease management. As culture-based diagnoses are associated with fundamental drawbacks, we used terminal restriction fragment (T-RF) length polymorphism profiling and 16S rRNA clone data to characterize, without prior cultivation, the bacterial community in 71 sputa from 34 adult CF patients. Nineteen species from 15 genera were identified in 53 16S rRNA clones from three patients. Of these, 15 species have not previously been reported in CF lung infections and many were species requiring strict anaerobic conditions for growth. The species richness and evenness were determined from the T-RF length and volume for the 71 profiles. Species richness was on average 13.3 ± 7.9 per sample and 13.4 ± 6.7 per patient. On average, the T-RF bands of the lowest and highest volumes represented 0.6 and 59.2% of the total volume in each profile, respectively. The second through fifth most dominant T-RF bands represented 15.3, 7.5, 4.7, and 2.8% of the total profile volume, respectively. On average, the remaining T-RF bands represented 10.2% of the total profile volume. The T-RF band corresponding to Pseudomonas aeruginosa had the highest volume in 61.1% of the samples. However, 18 other T-RF band lengths were dominant in at least one sample. In conclusion, this reveals the enormous complexity of bacteria within the CF lung. Although their significance is yet to be determined, these findings alter our perception of CF lung infections.
* Corresponding author. Mailing address: Division of Life Sciences, King's College London, London SE1 9NN, United Kingdom. Phone: 44 020 7848 4670. Fax: 44 020 7848 4500. E-mail: kenneth.bruce{at}kcl.ac.uk.
Journal of Clinical Microbiology, November 2004, p. 5176-5183, Vol. 42, No. 11
0095-1137/04/$08.00+0 DOI: 10.1128/JCM.42.11.5176-5183.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.
This article has been cited by other articles:
-
Elborn, J S.
(2008). Identification and management of unusual pathogens in cystic fibrosis. JRSM
101: 2-5
[Full Text]
-
Tunney, M. M., Field, T. R., Moriarty, T. F., Patrick, S., Doering, G., Muhlebach, M. S., Wolfgang, M. C., Boucher, R., Gilpin, D. F., McDowell, A., Elborn, J. S.
(2008). Detection of Anaerobic Bacteria in High Numbers in Sputum from Patients with Cystic Fibrosis. Am. J. Respir. Crit. Care Med.
177: 995-1001
[Abstract]
[Full Text]
-
Harris, J. K., De Groote, M. A., Sagel, S. D., Zemanick, E. T., Kapsner, R., Penvari, C., Kaess, H., Deterding, R. R., Accurso, F. J., Pace, N. R.
(2007). Molecular identification of bacteria in bronchoalveolar lavage fluid from children with cystic fibrosis. Proc. Natl. Acad. Sci. USA
104: 20529-20533
[Abstract]
[Full Text]
-
Hybiske, K., Fu, Z., Schwarzer, C., Tseng, J., Do, J., Huang, N., Machen, T. E.
(2007). Effects of cystic fibrosis transmembrane conductance regulator and {Delta}F508CFTR on inflammatory response, ER stress, and Ca2+ of airway epithelia. Am. J. Physiol. Lung Cell. Mol. Physiol.
293: L1250-L1260
[Abstract]
[Full Text]
-
Palmer, K. L., Brown, S. A., Whiteley, M.
(2007). Membrane-Bound Nitrate Reductase Is Required for Anaerobic Growth in Cystic Fibrosis Sputum. J. Bacteriol.
189: 4449-4455
[Abstract]
[Full Text]
-
Thies, F. L., Konig, W., Konig, B.
(2007). Rapid characterization of the normal and disturbed vaginal microbiota by application of 16S rRNA gene terminal RFLP fingerprinting. J Med Microbiol
56: 755-761
[Abstract]
[Full Text]
-
Harrison, F.
(2007). Microbial ecology of the cystic fibrosis lung. Microbiology
153: 917-923
[Abstract]
[Full Text]
-
(2006). Poster presentations. Thorax
61: ii57-ii133
[Full Text]
-
Danovaro, R., Luna, G. M., Dell'Anno, A., Pietrangeli, B.
(2006). Comparison of Two Fingerprinting Techniques, Terminal Restriction Fragment Length Polymorphism and Automated Ribosomal Intergenic Spacer Analysis, for Determination of Bacterial Diversity in Aquatic Environments. Appl. Environ. Microbiol.
72: 5982-5989
[Abstract]
[Full Text]
-
Machen, T. E.
(2006). Innate immune response in CF airway epithelia: hyperinflammatory?. Am. J. Physiol. Cell Physiol.
291: C218-C230
[Abstract]
[Full Text]
-
Singh, A., Goering, R. V., Simjee, S., Foley, S. L., Zervos, M. J.
(2006). Application of Molecular Techniques to the Study of Hospital Infection. Clin. Microbiol. Rev.
19: 512-530
[Abstract]
[Full Text]
-
Rogers, G. B., Carroll, M. P., Serisier, D. J., Hockey, P. M., Jones, G., Kehagia, V., Connett, G. J., Bruce, K. D.
(2006). 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.. J. Clin. Microbiol.
44: 2601-2604
[Abstract]
[Full Text]
-
Randell, S. H., Boucher, R. C., for the University of North Carolina Virtual Lung,
(2006). Effective Mucus Clearance Is Essential for Respiratory Health. Am. J. Respir. Cell Mol. Bio.
35: 20-28
[Full Text]
-
Bernier, S. P., Sokol, P. A.
(2005). Use of Suppression-Subtractive Hybridization To Identify Genes in the Burkholderia cepacia Complex That Are Unique to Burkholderia cenocepacia. J. Bacteriol.
187: 5278-5291
[Abstract]
[Full Text]
Copyright © 2004 by the American Society for Microbiology. All rights reserved.