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Staphylococcus aureus resists human defensins by production of staphylokinase, a novel bacterial evasion mechanism

Jin, Tao, 1973 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för invärtesmedicin, Avdelningen för reumatologi och inflammationsforskning,Institute of Internal Medicine, Dept of Rheumatology and Inflammation Research
Bokarewa, Maria, 1963 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för invärtesmedicin, Avdelningen för reumatologi och inflammationsforskning,Institute of Internal Medicine, Dept of Rheumatology and Inflammation Research
Foster, T. (författare)
visa fler...
Mitchell, J. (författare)
Higgins, J. (författare)
Tarkowski, Andrej, 1951 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för invärtesmedicin, Avdelningen för reumatologi och inflammationsforskning,Institute of Internal Medicine, Dept of Rheumatology and Inflammation Research
visa färre...
 (creator_code:org_t)
2004
2004
Engelska.
Ingår i: J Immunol. - 0022-1767. ; 172:2, s. 1169-76
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Alpha-defensins are peptides secreted by polymorphonuclear cells and provide antimicrobial protection mediated by disruption of the integrity of bacterial cell walls. Staphylokinase is an exoprotein produced by Staphylococcus aureus, which activates host plasminogen. In this study, we analyzed the impact of interaction between alpha-defensins and staphylokinase on staphylococcal growth. We observed that staphylokinase induced extracellular release of alpha-defensins from polymorphonuclear cells. Moreover, a direct binding between alpha-defensins and staphylokinase was shown to result in a complex formation. The biological consequence of this interaction was an almost complete inhibition of the bactericidal effect of alpha-defensins. Notably, staphylokinase with blocked plasminogen binding site still retained its ability to neutralize the bactericidal effect of alpha-defensins. In contrast, a single mutation of a staphylokinase molecule at position 74, substituting lysine for alanine, resulted in a 50% reduction of its alpha-defensin-neutralizing properties. The bactericidal properties of alpha-defensins were tested in 19 S. aureus strains in vitro and in a murine model of S. aureus arthritis. Staphylococcal strains producing staphylokinase were protected against the bactericidal effect of alpha-defensins. When staphylokinase was added to staphylokinase-negative S. aureus cultures, it almost totally abrogated the effect of alpha-defensins. Finally, human neutrophil peptide 2 injected intra-articularly along with bacteria alleviated joint destruction. In this study, we report a new property of staphylokinase, its ability to induce secretion of defensins, to complex bind them and to neutralize their bactericidal effect. Staphylokinase production may therefore be responsible in vivo for defensin resistance during S. aureus infections.

Nyckelord

Adult
Aged
Aged
80 and over
Animals
Arthritis
Experimental/immunology/microbiology/prevention & control
Enzyme Activation/physiology
Female
Humans
Immunity
Natural
Male
Metalloendopeptidases/*biosynthesis/metabolism/pharmacology
Mice
Microbial Sensitivity Tests
Middle Aged
Nasal Mucosa/enzymology/microbiology
Neutrophils/microbiology/secretion
Plasminogen/antagonists & inhibitors/metabolism
Recombinant Proteins/metabolism
Staphylococcal Infections/immunology/microbiology/prevention & control
development/*immunology/isolation & purification
inhibitors/metabolism/*physiology/therapeutic use

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