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Title: Drosomycin-like defensin, a human homologue of Drosophila melanogaster drosomycin with antifungal activity.
Author(s): Simon, A. (269055924)
Kullberg, B.J. (074528858)
Tripet, B.
Boerman, O.C. (074891006)
Zeeuwen, P.L.J.M. (267539924)
Ven-Jongekrijg, J. van der (29897455X)
Verweij, P.
Schalkwijk, J. (071581529)
Hodges, R.
Meer, J.W.M. van der (070708525)
Netea, M.G. (171035860)
Publication year: 2008
Document type: Article / Letter to editor
Journal: Antimicrobial Agents and Chemotherapy
ISSN: 0066-4804
Volume: vol. 52
Issue: iss. 4
Start page: p. 1407
End page: p. 1412
Abstract: Innate antifungal defense in Drosophila melanogaster relies on the activation of the Toll molecule and the release of drosomycin, a defensin-like molecule with antifungal properties. Ten human homologues of Toll have been described, with central roles in activation of the innate host defense. In the present study, we report a putative human homologue of the Drosophila-derived drosomycin, designated drosomycin-like defensin (DLD). Synthetic DLD displays a broad spectrum of activity against Aspergillus spp. and other clinically relevant filamentous fungi. These effects are specific for filamentous fungi; no activity has been found against yeasts or gram-positive or gram-negative bacteria. Synthetic DLD also displays immunomodulatory effects on Aspergillus-stimulated cytokine production. In addition, we show the expression of DLD mRNA in several human tissues, particularly in the skin, consistent with its putative role as a defensin against invading microorganisms. This is the first indication of an endogenous human peptide with specific antifungal activity, which is probably central in the defense against infections with molds.
Subject: NCMLS 1: Immunity, infection and tissue repair
NCMLS 1: Immunity, infection and tissue repair
UMCN 4.1: Microbial pathogenesis and host defense
UMCN 4.2: Chronic inflammation and autoimmunity
Organization: Dermatology
General Internal Medicine
Nuclear Medicine
Appears in Collections:Academic bibliography

Please use this identifier to cite or link to this item: http://hdl.handle.net/2066/70510

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