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PMID: 19919305 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Constitutive expression of the antimicrobial peptide RNase 7 is associated with Staphylococcus aureus infection of the skin.

The Journal of infectious diseases ·Vol. 200 ·No. 12 ·2009-12-15 ·Pages 1907-15

Zanger P, Holzer J, Schleucher R, Steffen H, Schittek B, Gabrysch S

Abstract

Staphylococcus aureus infections of the skin are a public health problem of growing importance. Antimicrobial peptides in human skin are believed to play an important role in innate defense against intruding pathogens. This study aimed to clarify whether their baseline expression influences the propensity of healthy individuals to develop S. aureus-positive skin infections. Using real-time polymerase chain reaction technique and a prospective case-control design, we determined the expression of messenger RNA coding for human beta-defensin 2 and 3 as well as RNase 7 in unaffected skin of 20 travelers returning with Staphylococcus aureus-positive skin infection (case patients) relative to levels in 40 matched control subjects. Expression of RNase 7 was found to be 64% higher in unaffected skin of control subjects, compared with unaffected skin of case patients (95% confidence interval, 17%-131%; P = .007). This association remained stable after controlling for S. aureus nasal carriage, smoking, level of accommodation, and history of allergy. No such association was present for human beta-defensin 2 or 3. In conjunction with the existing evidence from in vitro studies, these findings suggest that antimicrobial peptides found at high baseline levels in healthy skin, such as RNase 7, confer protection against S. aureus infection of the skin.

MeSH Terms
Adult Antimicrobial Cationic Peptides/biosynthesis Case-Control Studies Female Gene Expression Profiling Humans Male Reverse Transcriptase Polymerase Chain Reaction/methods Ribonucleases/biosynthesis Staphylococcal Skin Infections/immunology,microbiology Staphylococcus aureus/immunology,isolation & purification Young Adult beta-Defensins/biosynthesis
Chemicals
Antimicrobial Cationic Peptides DEFB103A protein, human DEFB4A protein, human beta-Defensins Ribonucleases Ribonuclease 7
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Zanger Philipp
Institut für Tropenmedizin, Eberhard Karls Universität, 72074 Tübingen, Germany. philipp.zanger@med.uni-tuebingen.de
Holzer Johannes
Schleucher Regina
Steffen Heiko
Schittek Birgit
Gabrysch Sabine
Article Info
Journal
The Journal of infectious diseases
Abbr.
J Infect Dis
ISSN
1537-6613
Published
2009-12-15
Pages
1907-15
Language
English
Region
United States
NLM ID
0413675
Subset
IM
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