Haemophilus influenzae Protein E Binds to the Extracellular Matrix by Concurrently Interacting With Laminin and Vitronectin

被引:44
作者
Hallstrom, Teresia [3 ]
Singh, Birendra
Resman, Fredrik
Blom, Anna M. [1 ]
Morgelin, Matthias [2 ]
Riesbeck, Kristian [1 ]
机构
[1] Lund Univ, Skane Univ Hosp, Dept Lab Med Malmo, SE-20502 Malmo, Sweden
[2] Lund Univ, Sect Clin & Expt Infect Med, Dept Clin Sci, SE-20502 Malmo, Sweden
[3] Hans Knoell Inst, Dept Infect Biol, Leibniz Inst Nat Prod Res & Infect Biol, Jena, Germany
基金
瑞典研究理事会;
关键词
PATHOGEN MORAXELLA-CATARRHALIS; SURFACE PROTEIN; EPITHELIAL-CELLS; FIBRONECTIN; ADHESIN; VIRULENCE; MEDIA; A1;
D O I
10.1093/infdis/jir459
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Nontypeable Haemophilus influenzae (NTHi) causes otitis media and is commonly found in patients with chronic obstructive pulmonary disease (COPD). Adhesins are important for bacterial attachment and colonization. Protein E (PE) is a recently characterized ubiquitous 16 kDa adhesin with vitronectin-binding capacity that results in increased survival in serum. In addition to PE, NTHi utilizes Haemophilus adhesion protein (Hap) that binds to the basement-membrane glycoprotein laminin. We show that most clinical isolates bind laminin and that both Hap and PE are crucial for the NTHi-dependent interaction with laminin as revealed with different mutants. The laminin-binding region is located at the N-terminus of PE, and PE binds to the heparin-binding C-terminal globular domain of laminin. PE simultaneously attracts vitronectin and laminin at separate binding sites, proving the multifunctional nature of the adhesin. This previously unknown PE-dependent interaction with laminin may contribute to NTHi colonization, particularly in smokers with COPD.
引用
收藏
页码:1065 / 1074
页数:10
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