Dynamic interaction between airway epithelial cells and Staphylococcus aureus

被引:38
作者
da Silva, MCA
Zahm, JM
Gras, D
Bajolet, O
Abely, M
Hinnrasky, J
Milliot, M
de Assis, MC
Hologne, C
Bonnet, N
Merten, M
Plotkowski, MC
Puchelle, E
机构
[1] CHU Maison Blanche, INSERM, Unite Mixte Rech S 514, Inst Federatif Rech 53, F-51092 Reims, France
[2] INSERM, Equipe Propre 0014, F-54505 Vandoeuvre Les Nancy, France
[3] Univ Fed Rio de Janeiro, Inst Microbiol Prof Paulo de Goes, BR-21941590 Rio De Janeiro, Brazil
[4] State Univ Rio de Janeiro, Dept Microbiol & Immunol, BR-20551030 Rio De Janeiro, Brazil
关键词
videomicroscopy; secretory leukoproteinase inhibitor; alpha-toxin; airway cell damage; bacterial adherence and internalization;
D O I
10.1152/ajplung.00256.2003
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Staphylococcus aureus is a major cause of pulmonary infection, particularly in cystic fibrosis (CF) patients. However, few aspects of the interplay between S. aureus and host airway epithelial cells have been investigated thus far. We investigated by videomicroscopy the time- and bacterial concentration-dependent (10(4), 10(6), and 10(8) CFU/ml) effect of S. aureus on adherence, internalization, and the associated damage of the airway epithelial cells. The balance between the secretion by S. aureus of the alpha-toxin virulence factor and by the airway cells of the antibacterial secretory leukoproteinase inhibitor (SLPI) was also analyzed. After 1 h of interaction, whatever the initial bacterial concentration, a low percentage of S. aureus (<8%) adhered to airway cells, and no airway epithelial cell damage was observed. In contrast, after 24 h of incubation, more bacteria adhered to airway epithelial cells, internalized bacteria were observed, and a bacterial concentration-dependent effect on airway cell damage was observed. At 24 h, most airway cells incubated with bacteria at 10(8) CFU/ml exhibited a necrotic phenotype. The necrosis was preceded by a transient apoptotic process. In parallel, we observed a time- and bacterial concentration-dependent decrease in SLPI and increase in alpha-toxin expression. These results suggest that airway cells can defend against S. aureus in the early stages of infection. However, in later phases, there is a marked imbalance between the bactericidal capacity of host cells and bacterial virulence. These findings reinforce the potential importance of S. aureus in the pathogenicity of airway infections, including those observed early in CF patients.
引用
收藏
页码:L543 / L551
页数:9
相关论文
共 36 条
[1]   α-toxin is a mediator of Staphylococcus aureus-induced cell death and activates caspases via the intrinsic death pathway independently of death receptor signaling [J].
Bantel, H ;
Sinha, B ;
Domschke, W ;
Peters, G ;
Schulze-Osthoff, K ;
Jänicke, RU .
JOURNAL OF CELL BIOLOGY, 2001, 155 (04) :637-647
[2]   QUALITATIVE AND QUANTITATIVE MICROBIOLOGICAL ANALYSIS OF SPUTA OF 102 PATIENTS WITH CYSTIC-FIBROSIS [J].
BAUERNFEIND, A ;
BERTELE, RM ;
HARMS, K ;
HORL, G ;
JUNGWIRTH, R ;
PETERMULLER, C ;
PRZYKLENK, B ;
WEISSLEINPFISTER, C .
INFECTION, 1987, 15 (04) :270-277
[3]   Microbiology of sputum from patients at cystic fibrosis centers in the United States [J].
Burns, JL ;
Emerson, J ;
Stapp, JR ;
Yim, DL ;
Krzewinski, J ;
Louden, L ;
Ramsey, BW ;
Clausen, CR .
CLINICAL INFECTIOUS DISEASES, 1998, 27 (01) :158-163
[4]   CACO-2 AND IEC-18 INTESTINAL EPITHELIAL-CELLS EXERT BACTERICIDAL ACTIVITY THROUGH AN OXIDANT-DEPENDENT PATHWAY [J].
DEITCH, EA ;
HASKEL, Y ;
CRUZ, N ;
XU, DZ ;
KVIETYS, PR .
SHOCK, 1995, 4 (05) :345-350
[5]   Transcriptional regulation of β-defensin gene expression in tracheal epithelial cells [J].
Diamond, G ;
Kaiser, V ;
Rhodes, J ;
Russell, JP ;
Bevins, CL .
INFECTION AND IMMUNITY, 2000, 68 (01) :113-119
[6]   STAPHYLOCOCCUS-AUREUS INDUCES TISSUE FACTOR EXPRESSION IN CULTURED HUMAN CARDIAC-VALVE ENDOTHELIUM [J].
DRAKE, TA ;
PANG, M .
JOURNAL OF INFECTIOUS DISEASES, 1988, 157 (04) :749-756
[7]   Fibronectin binding protein and host cell tyrosine kinase are required for internalization of Staphylococcus aureus by epithelial cells [J].
Dziewanowska, K ;
Patti, JM ;
Deobald, CF ;
Bayles, KW ;
Trumble, WR ;
Bohach, GA .
INFECTION AND IMMUNITY, 1999, 67 (09) :4673-4678
[8]   Staphylococcus aureus α-toxin-induced cell death:: predominant necrosis despite apoptotic caspase activation [J].
Essmann, F ;
Bantel, H ;
Totzke, G ;
Engels, IH ;
Sinha, B ;
Schulze-Osthoff, K ;
Jänicke, RU .
CELL DEATH AND DIFFERENTIATION, 2003, 10 (11) :1260-1272
[9]   Cell-wall determinants of the bactericidal action of group IIA phospholipase A2 against Gram-positive bacteria [J].
Foreman-Wykert, AK ;
Weinrauch, Y ;
Elsbach, P ;
Weiss, J .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 103 (05) :715-721
[10]   DISTRIBUTION OF ANTILEUKOPROTEASE IN UPPER RESPIRATORY MUCOSA [J].
FRYKSMARK, U ;
POLLING, A ;
OHLSSON, K ;
TEGNER, H .
ANNALS OF OTOLOGY RHINOLOGY AND LARYNGOLOGY, 1982, 91 (03) :268-271