Synergistic and additive killing by antimicrobial factors found in human airway surface liquid

被引:261
作者
Singh, PK
Tack, BF
McCray, PB
Welsh, MJ
机构
[1] Univ Iowa, Coll Med, Howard Hughes Med Inst, Iowa City, IA 52242 USA
[2] Univ Iowa, Coll Med, Dept Internal Med, Iowa City, IA 52242 USA
[3] Univ Iowa, Coll Med, Dept Microbiol, Iowa City, IA 52242 USA
[4] Univ Iowa, Coll Med, Dept Pediat, Iowa City, IA 52242 USA
[5] Univ Iowa, Coll Med, Dept Physiol & Biophys, Iowa City, IA 52242 USA
关键词
cystic fibrosis; innate immunity; lysozyme; beta-defensins; lactoferrin;
D O I
10.1152/ajplung.2000.279.5.L799
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
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 beta -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.
引用
收藏
页码:L799 / L805
页数:7
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