Scientists develop a fatty 'kryptonite' to defeat multidrug-resistant 'Super bugs'

According to a researcher involved in the study, Richard Epand, Ph.D. from the Department of Biochemistry and Biomedical Science at McMaster University in Hamilton, Ontario, Canada, "This study may contribute to overcoming the lethal effects of drug resistant bacteria that is becoming an increasing clinical problem, particularly in hospitals."

To make their discovery, Epand and colleagues conducted experiments using groups of mice infected with lethal doses of multidrug-resistant Escherichia coli (E. coli). Researchers then treated the mice with conventional drug combinations or drug combinations encapsulated in lipid mixtures. They found that certain lipid mixtures caused the drugs to act together in a synergistic manner. In this form, the drugs were much more effective in increasing the survival rate of the mice because they overcame the cellular mechanisms used by these bacteria to defeat therapeutic agents. This study also demonstrated a novel use of a new family of antimicrobial agents called oligo-acyl-lysyls, which have the potential to be combined with other drugs and lipid mixtures with similar properties to yield a platform for other specific applications.

"As we've seen in the recent E.Coli outbreak in Germany, bacteria can mutate to become super bugs that resist antibiotics," said Gerald Weissmann, M.D., Editor-in-Chief of The FASEB Journal, "Thanks to this new, lipid-based antibiotic therapy. multidrug-resistant bacteria may begin to look more like Jimmy Olsen and a lot less like Superman."

More information: Hadar Sarig, Dafna Ohana, Raquel F. Epand, Amram Mor, and Richard M. Epand. Functional studies of cochleate assemblies of an oligo-acyl-lysyl with lipid mixtures for combating bacterial multidrug resistance. FASEB J; doi:10.1096/fj.11-183764

Provided by Federation of American Societies for Experimental Biology