Susceptibility of Staphylococcus aureus bacteremia strains to different skin-derived antimicrobial proteins
详细信息    查看全文
  • 作者:Bente K?ten (1)
    Karsten Becker (2)
    Rainer Podschun (3)
    Christof von Eiff (2)
    Ulf Meyer-Hoffert (1) umeyerhoffert@dermatology.uni-kiel.de
    Jürgen Harder (1)
    Regine Gl?ser (1) rglaeser@dermatology.uni-kiel.de
  • 关键词:Antimicrobial peptides – Innate immunity – Colonization – Bacterial flora – S. aureus
  • 刊名:Archives of Dermatological Research
  • 出版年:2012
  • 出版时间:October 2012
  • 年:2012
  • 卷:304
  • 期:8
  • 页码:633-637
  • 全文大小:235.7 KB
  • 参考文献:1. Fode P, Larsen AR, Feenstra B, Jespersgaard C, Skov RL, Stegger M, Fowler VG Jr, Andersen PS (2012) Genetic variability in beta-defensins is not associated with susceptibility to Staphylococcus aureus bacteremia. PLoS One 7(2):e32315
    2. Glaser R, Harder J, Lange H, Bartels J, Christophers E, Schroder JM (2005) Antimicrobial psoriasin (S100A7) protects human skin from Escherichia coli infection. Nat Immunol 6(1):57–64
    3. Habets MG, Brockhurst MA (2012) Therapeutic antimicrobial peptides may compromise natural immunity. Biol Lett 8(3):416–418
    4. Habets MG, Rozen DE, Brockhurst MA (2012) Variation in Streptococcus pneumoniae susceptibility to human antimicrobial peptides may mediate intraspecific competition. Proc Biol Sci 279(1743):3803–3811
    5. Harder J, Bartels J, Christophers E, Schroder JM (2001) Isolation and characterization of human beta -defensin-3, a novel human inducible peptide antibiotic. J Biol Chem 276(8):5707–5713
    6. Harder J, Schroder JM (2002) RNase 7, a novel innate immune defense antimicrobial protein of healthy human skin. J Biol Chem 277(48):46779–46784
    7. Iwatsuki K, Yamasaki O, Morizane S, Oono T (2006) Staphylococcal cutaneous infections: invasion, evasion and aggression. J Dermatol Sci 42(3):203–214
    8. Kisich KO, Howell MD, Boguniewicz M, Heizer HR, Watson NU, Leung DY (2007) The constitutive capacity of human keratinocytes to kill Staphylococcus aureus is dependent on beta-defensin 3. J Invest Dermatol 127(10):2368–2380
    9. Koten B, Simanski M, Glaser R, Podschun R, Schroder JM, Harder J (2009) RNase 7 contributes to the cutaneous defense against Enterococcus faecium. PLoS ONE 4(7):e6424
    10. Laudien M, Dressel S, Harder J, Glaser R (2011) Differential expression pattern of antimicrobial peptides in nasal mucosa and secretion. Rhinology 49(1):107–111
    11. Lippross S, Klueter T, Steubesand N, Oestern S, Mentlein R, Hildebrandt F, Podschun R, Pufe T, Seekamp A, Varoga D (2012) Multiple trauma induces serum production of host defence peptides. Injury 43(2):137–142
    12. Otto M (2010) Staphylococcus colonization of the skin and antimicrobial peptides. Expert Rev Dermatol 5(2):183–195
    13. Peschel A, Sahl HG (2006) The co-evolution of host cationic antimicrobial peptides and microbial resistance. Nat Rev Microbiol 4(7):529–536
    14. Sahly H, Schubert S, Harder J, Rautenberg P, Ullmann U, Schroder J, Podschun R (2003) Burkholderia is highly resistant to human Beta-defensin 3. Antimicrob Agents Chemother 47(5):1739–1741
    15. Simanski M, Dressel S, Glaser R, Harder J (2010) RNase 7 protects healthy skin from Staphylococcus aureus colonization. J Invest Dermatol 130(12):2836–2838
    16. von Eiff C, Becker K, Machka K, Stammer H, Peters G (2001) Nasal carriage as a source of Staphylococcus aureus bacteremia. Study Group. N Engl J Med 344(1):11–16
  • 作者单位:1. Department of Dermatology, University Hospital Schleswig-Holstein, Campus Kiel, Kiel, Germany2. Institute of Medical Microbiology, University Hospital of Münster, Münster, Germany3. Institute for Infection Medicine, University Hospital Schleswig-Holstein, Campus Kiel, Kiel, Germany
  • ISSN:1432-069X
文摘
Staphylococcus aureus is a major human pathogen causing cutaneous infections to life-threatening bacteremia. These infections are often caused by strains derived from the own microflora suggesting that a disturbed epidermal barrier may promote invasion of S. aureus. Antimicrobial peptides and proteins (AMP) such as human beta-defensin-3 and RNase 7 contribute to control the colonization of S. aureus on the skin surface. This leads to the hypothesis that strains with a decreased susceptibility toward skin-derived AMP may better overcome the innate cutaneous defence barrier increasing the possibility of invading into the blood stream. To address this hypothesis we determined whether S. aureus strains from bacteremia patients are less susceptible to various skin-derived AMP than strains from healthy carriers. No differences in the AMP-killing activity against bacteremia-derived S. aureus and control strains were detected suggesting that the onset of S. aureus bacteremia is not based on the varying susceptibilities against skin-derived AMP.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700