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Novel alternatives to antibiotics: bacteriophages, bacterial cell wall hydrolases, and antimicrobial peptides.

A. Parisien, B. Allain, J. Zhang, R. Mandeville, C.Q.

 Lan. Journal of Applied Microbiology.  Jan 2008 v104 i1 p1(13).

Author's Abstract:

To purchase or authenticate to the full-text of this article, please visit this link: http://dx.doi.org/10.1111/j.1365-2672.2007.03498.x

Byline: A. Parisien (1), B. Allain (2), J. Zhang (1), R. Mandeville (2), C.Q. Lan (1)

Keywords:

alternative antibacterials; antibiotics resistance; antimicrobial peptide; bacteriophage; lytic enzyme; virolysin

Abstract:

Summary

Extensive research has been conducted on the development of three groups of naturally occurring antimicrobials as novel alternatives to antibiotics: bacteriophages (phages), bacterial cell wall hydrolases (BCWH), and antimicrobial peptides (AMP). Phage therapies are highly efficient, highly specific, and relatively cost-effective. However, precautions have to be taken in the selection of phage candidates for therapeutic applications as some phages may encode toxins and others may, when integrated into host bacterial genome and converted to prophages in a lysogenic cycle, lead to bacterial immunity and altered virulence. BCWH are divided into three groups: lysozymes, autolysins, and virolysins. Among them, virolysins are the most promising candidates as they are highly specific and have the capability to rapidly lyse antibiotic-resistant bacteria on a generally species-specific basis. Finally, AMP are a family of natural proteins produced by eukaryotic and prokaryotic organisms or encoded by phages. AMP are of vast diversity in term of size, structure, mode of action, and specificity and have a high potential for clinical therapeutic applications.

Author Affiliation:

(1)Department of Chemical Engineering, University of Ottawa, Ottawa, Canada

(2)Biophage Pharma Inc., 6100 Royalmount, Montreal, Quebec, Canada H4P 2R2

Article History:

2007/0290: received 23 February 2007, revised 28 May 2007 and accepted 11 June 2007

Article note:

Christopher Q. Lan, Department of Chemical Engineering, University of Ottawa, 161 Louis Pasteur St., Ottawa, ON, K1N 6N5, Canada., E-mail: clan@uottawa.ca


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