| Literature DB >> 21233507 |
Alan R Hauser1, Manu Jain, Maskit Bar-Meir, Susanna A McColley.
Abstract
A select group of microorganisms inhabit the airways of individuals with cystic fibrosis. Once established within the pulmonary environment in these patients, many of these microbes adapt by altering aspects of their structure and physiology. Some of these microbes and adaptations are associated with more rapid deterioration in lung function and overall clinical status, whereas others appear to have little effect. Here we review current evidence supporting or refuting a role for the different microbes and their adaptations in contributing to poor clinical outcomes in cystic fibrosis.Entities:
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Year: 2011 PMID: 21233507 PMCID: PMC3021203 DOI: 10.1128/CMR.00036-10
Source DB: PubMed Journal: Clin Microbiol Rev ISSN: 0893-8512 Impact factor: 26.132