Phylogenetic and metabolic diversity of bacteria associated with cystic fibrosis

Adam M. Guss, Guus Roeselers, Irene L.G. Newton, C. Robert Young, Vanja Klepac-Ceraj, Stephen Lory, Colleen M. Cavanaugh

Research output: Contribution to journalArticlepeer-review

157 Scopus citations

Abstract

In patients afflicted with cystic fibrosis (CF), morbidity and mortality are primarily associated with the adverse consequences of chronic microbial bronchial infections, which are thought to be caused by a few opportunistic pathogens. However, recent evidence suggests the presence of other microorganisms, which may significantly affect the course and outcome of the infection. Using a combination of 16S rRNA gene clone libraries, bacterial culturing and pyrosequencing of barcoded 16S rRNA amplicons, the microbial communities present in CF patient sputum samples were examined. In addition to previously recognized CF pathogens such as Pseudomonas aeruginosa and Staphylococcus aureus, > 60 phylogenetically diverse bacterial genera that are not typically associated with CF pathogenesis were also detected. A surprisingly large number of fermenting facultative and obligate anaerobes from multiple bacterial phyla was present in each sample. Many of the bacteria and sequences found were normal residents of the oropharyngeal microflora and with many containing opportunistic pathogens. Our data suggest that these undersampled organisms within the CF lung are part of a much more complex microbial ecosystem than is normally presumed. Characterization of these communities is the first step in elucidating potential roles of diverse bacteria in disease progression and to ultimately facilitate advances in CF therapy.

Original languageEnglish
Pages (from-to)20-29
Number of pages10
JournalISME Journal
Volume5
Issue number1
DOIs
StatePublished - Jan 2011
Externally publishedYes

Funding

We thank the Children’s Hospital Boston Pulmonary Fellows for sample collection, Joe Jones for technical advice on pyrosequencing and Kristina Fontanez for assistance with the pyrosequencing analysis. This work was supported by a Rubicon grant by the Netherlands Organisation for Scientific Research (NWO) to GR, a Harvard University Microbial Sciences Initiative (MSI) postdoctoral fellowship to AMG, a Howard Hughes Predoctoral Fellowship to ILGN, an internal grant from the University of South Carolina Office of Research and Health Sciences to CRY, grants from NIH (GM068516) to SL, and NSF (OCE-0453901) and Harvard University Center for the Environment (HUCE) to CMC.

FundersFunder number
Harvard University Microbial Sciences Initiative
University of South Carolina Office of Research and Health Sciences
National Science FoundationOCE-0453901
National Institutes of Health
National Institute of General Medical SciencesR01GM068516
Center for the Environment, Harvard University
Marketing Science Institute
Nederlandse Organisatie voor Wetenschappelijk Onderzoek

    Keywords

    • CF
    • Pseudomonas aeruginosa
    • lung
    • microbial diversity
    • polymicrobial disease
    • pyrosequencing

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