Journal article
Synergistic and additive killing by antimicrobial factors found in human airway surface liquid
American journal of physiology. Lung cellular and molecular physiology, Vol.279(5), pp.L799-L805
11/01/2000
DOI: 10.1152/ajplung.2000.279.5.L799
PMID: 11053013
Abstract
Airway surface liquid contains multiple factors thought to provide a first line of defense against bacteria deposited in the airways. Although the antimicrobial action of individual factors has been studied, less is known about how they work in combination. We examined the combined action of six antimicrobial peptides found in airway surface liquid. The paired combinations of lysozyme-lactoferrin, lysozyme-secretory leukocyte protease inhibitor (SLPI), and lactoferrin-SLPI were synergistic. The triple combination of lysozyme, lactoferrin, and SLPI showed even greater synergy. Other combinations involving the human β-defensins, LL-37, and tobramycin (often administered to cystic fibrosis patients by inhalation) were additive. Because the airway surface liquid salt concentration may be elevated in cystic fibrosis patients, we examined the effect of salt on the synergistic combinations. As the ionic strength increased, synergistic interactions were lost. Our data suggest that the antibacterial potency of airway surface liquid may be significantly increased by synergistic and additive interactions between antimicrobial factors. These results also suggest that increased salt concentrations that may exist in cystic fibrosis could inhibit airway defenses by diminishing these synergistic interactions.
Details
- Title: Subtitle
- Synergistic and additive killing by antimicrobial factors found in human airway surface liquid
- Creators
- Pradeep K Singh - Internal MedicineBrian F Tack - MicrobiologyPaul B McCray - Pediatrics, andMichael J Welsh - Howard Hughes Medical Institute, and Departments of, Internal Medicine,, Physiology and Biophysics, University of Iowa College of Medicine, Iowa City, Iowa 52242
- Resource Type
- Journal article
- Publication Details
- American journal of physiology. Lung cellular and molecular physiology, Vol.279(5), pp.L799-L805
- DOI
- 10.1152/ajplung.2000.279.5.L799
- PMID
- 11053013
- NLM abbreviation
- Am J Physiol Lung Cell Mol Physiol
- ISSN
- 1040-0605
- eISSN
- 1522-1504
- Publisher
- American Physiological Society
- Language
- English
- Date published
- 11/01/2000
- Academic Unit
- Neurology; Molecular Physiology and Biophysics; Pulmonary, Critical Care, and Occupational Medicine; Microbiology and Immunology; Pulmonary Medicine; Stead Family Department of Pediatrics; Neurosurgery; Internal Medicine
- Record Identifier
- 9984020744302771
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