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Review
. 2015 Dec 31;11(12):e1005258.
doi: 10.1371/journal.ppat.1005258. eCollection 2015 Dec.

Cystic Fibrosis Lung Infections: Polymicrobial, Complex, and Hard to Treat

Laura M Filkins  1 , George A O'Toole  1
Affiliations
Review

Cystic Fibrosis Lung Infections: Polymicrobial, Complex, and Hard to Treat

Laura M Filkins et al. PLoS Pathog. .
No abstract available

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Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Fig 1
Fig 1. Cystic fibrosis lung infections are polymicrobial, complex, and challenging to treat.
The airways of patients with CF are colonized from various host (as indicated) and environmental (not depicted) sources. Patients subsequently develop chronic, polymicrobial infections composed of diverse bacterial, fungal, and viral organisms. These polymicrobial communities both influence and are impacted by their human host through complex, multifactorial interactions. As highlighted in the figure above and throughout this review, CF lung microbial communities encounter frequent antibiotic therapy, host immune factors, and an altered lung environment (including the presence of hypoxic [low oxygen] and anoxic [no oxygen] regions) throughout disease progression, all of which contribute to the development of chronic communities that often have decreased microbial diversity and are populated by organisms that have become highly adapted and resilient to treatment. The combination of diverse colonization sources, dynamic inter-domain interactions, microbial adaptation, environmental factors, and patient therapy mediates patient outcome. Eventually, chronic pulmonary infection culminates in a decline in lung function, which becomes most severe during pulmonary exacerbations and late stage disease progression. This steep decline in lung function ultimately leads to respiratory failure, the primary cause of morbidity and mortality in CF patients today [6]. Figure illustration and design copyright 2015 William Scavone and used with permission.
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