Plectasin has antibacterial activity and no affect on cell viability or IL-8 production

Animals and plants express endogenous peptide antibiotics called defensins. Defensins show broad-spectrum antimicrobial activity, even against bacteria that have resistance to conventional antibiotics, which has made them viable candidates for new antibiotics. However, human defensins have failed to...

Full description

Saved in:
Bibliographic Details
Published inBiochemical and biophysical research communications Vol. 374; no. 4; pp. 709 - 713
Main Authors Hara, Shintaro, Mukae, Hiroshi, Sakamoto, Noriho, Ishimoto, Hiroshi, Amenomori, Misato, Fujita, Hanako, Ishimatsu, Yuji, Yanagihara, Katsunori, Kohno, Shigeru
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 03.10.2008
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Animals and plants express endogenous peptide antibiotics called defensins. Defensins show broad-spectrum antimicrobial activity, even against bacteria that have resistance to conventional antibiotics, which has made them viable candidates for new antibiotics. However, human defensins have failed to reach the market because of their cytotoxic effects and non-antimicrobial bioactivities. Plectasin is a defensin that has shown promise but has not had its potentially negative effects clarified. To address this issue, we examined plectasin’s cytotoxicity in human cells using an AlamarBlue reduction assay, its interleukin (IL)-8-inducing capacity using real-time PCR and ELISA, and measured its MIC against bacteria. We confirmed that plectasin has specific antibacterial activity against Streptococcus pneumoniae. Plectasin showed no cytotoxicity to A549 cells, normal human bronchial epithelial cells, or lung fibroblasts, and it did not induce IL-8 transcription or production in A549 cells. Our results suggest that plectasin could be an inoffensive alternative antibiotic for clinical application.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0006-291X
1090-2104
DOI:10.1016/j.bbrc.2008.07.093