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JAC Advance Access originally published online on September 29, 2005
Journal of Antimicrobial Chemotherapy 2005 56(5):957-961; doi:10.1093/jac/dki350
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© The Author 2005. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved. For Permissions, please e-mail: journals.permissions@oxfordjournals.org

Cationic peptide of the male reproductive tract, HE2{alpha}, displays antimicrobial activity against Neisseria gonorrhoeae, Staphylococcus aureus and Enterococcus faecalis

M. Liao1,2,{dagger}, P. S. Ruddock3, A. S. Rizvi1, S. H. Hall4, F. S. French4 and J. R. Dillon1–3,*

1 Department of Biochemistry, Microbiology and Immunology, University of Ottawa, ON, Canada, K1H 8M5; 2 Centre for Research in Biopharmaceuticals and Biotechnology, University of Ottawa, ON, Canada, K1H 8M5; 3 Department of Biology, University of Ottawa, ON, Canada, K1H 8M5; 4 Laboratories for Reproductive Biology, University of North Carolina at Chapel Hill, Campus Box 7500, Chapel Hill, NC 27599, USA

Received 29 March 2005; returned 4 May 2005; revised 16 August 2005; accepted 8 September 2005


* Corresponding author. Present address. College of Arts and Science, University of Saskatchewan, Room 226, Arts Building, 9 Campus Drive, Saskatoon, SK, Canada, S7N 5A5. Tel: +1-306-9664232; Fax: +1-306-9668839; E-mail: j.dillon{at}usask.ca

Objectives: To analyse the in vitro antimicrobial effects of synthetic HE2{alpha} peptide against Neisseria gonorrhoeae, Staphylococcus aureus and Enterococcus faecalis.

Methods: The HE2{alpha} peptide was synthesized based on the C-terminal sequence of the HE2{alpha} protein. The bacterial strains tested included two antibiotic-susceptible strains of N. gonorrhoeae and four antibiotic-resistant clinical isolates, as well as S. aureus ATCC 29213 and E. faecalis ATCC 29212. Susceptibility determinations were carried out either in 0.7% casamino acids for N. gonorrhoeae isolates or in 10 mM phosphate buffer for S. aureus and E. faecalis strains. Antibacterial effects were measured in a dose- and time-dependent manner. After exposure to the peptide in solution, the number of viable cells was determined by counting colony forming units (cfu).

Results: The HE2{alpha} peptide exhibited time- and dose-dependent antibacterial effects on all N. gonorrhoeae isolates tested. S. aureus and E. faecalis strains were also susceptible to the peptide. All strains tested were susceptible to the peptide at high concentrations (50 or 100 mg/L) and some strains were susceptible to a peptide concentration of 25 mg/L.

Conclusions: The peptide HE2{alpha}, which is derived from the male urogenital tract, exhibits antibacterial activity against both Gram-positive and Gram-negative pathogens in vitro. The peptide is active against both antibiotic-susceptible and -resistant N. gonorrhoeae isolates. Further investigation of the antimicrobial properties of the peptide is warranted.

Keywords: susceptibility tests , antimicrobial peptides , sexually transmitted diseases , pathogenic bacteria


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