Pushing back against drug-resistant bugs

Jan 22, 2014
Microbiology: Pushing back against drug-resistant bugs
The Pseudomonas aeruginosa bacterium is a common cause of opportunistic infections in humans and has a tendency to acquire resistance to a number of standard antibiotics. Credit: US Centers for Disease Control and Prevention/Janice Haney Carr

Some pathogens can adapt to the presence of drugs that would normally be lethal, and such antibiotic-resistant microbes are now the scourge of hospitals worldwide. Discovering new antibiotics is a laborious process, but research from a team led by Yi Yan Yang of the A*STAR Institute of Bioengineering and Nanotechnology, Singapore, and James Hedrick of the IBM Almaden Research Center, United States, could breathe new life into existing drugs.

One of the standard escape mechanisms employed by bacteria such as Pseudomonas aeruginosa (see image) entails increased production of proteins that purge or break down drug molecules. Polymers that stick to and disrupt bacterial membranes offer an alternative means for killing resistant cells. However, at elevated concentrations these polymers can also inflict damage on bystander host cells. Yang and Hedrick's team explored whether a combination of polymers and antibiotics might offer a safer alternative that draws on the strengths of both approaches.

They generated two different polymers—which they combined with vitamin E, a standard component of the diet of humans—with chemical properties that enabled them to penetrate cell membranes. Both proved more toxic to microbes than the same polymers without vitamin E, efficiently killing P. aeruginosa as well as two other pathogens, the bacterium Staphylococcus aureus and the fungus Candida albicans. Microscopic analysis indicated that the polymers worked by punching holes in the outer membranes of bacterial and fungal cells. Importantly, none of these compounds proved seriously toxic to rat at their effective doses, suggesting that their effects should be relatively specific to their pathogenic targets.

The team subsequently evaluated whether such constructs could bolster antibiotics that tend to lose efficacy against P. aeruginosa. They took the vitamin E-linked polymer formulation that had performed the best against this bacterium and combined it with the doxycycline, streptomycin or penicillin G. While all three received a boost from being combined with the polymer, doxycycline showed the greatest promise, proving capable of effectively eradicating bacteria at very low concentrations of both the drug and polymer. This combination also appeared to generate a greater number of holes in the bacterial cell surface, despite doxycycline not normally damaging the outer membrane when acting on its own.

The researchers hypothesize that the two-pronged attack gives doxycycline rapid access to the cellular interior, thus overwhelming the microbe before it has the opportunity to eliminate the drug. "These synergistic combinations may provide a promising way for combating multi-drug resistance," concludes Yang.

Explore further: New way to fight antibiotic-resistant bacteria: Target human cells instead

More information: Ng, V. W. L., Ke, X., Lee, A. L. Z., Hedrick, J. L. & Yang, Y. Y. "Synergistic co-delivery of membrane-disrupting polymers with commercial antibiotics against highly opportunistic bacteria." Advanced Materials 25, 6730–6736 (2013). dx.doi.org/10.1002/adma.201302952

add to favorites email to friend print save as pdf

Related Stories

Recommended for you

Cell division, minus the cells

57 minutes ago

(Phys.org) —The process of cell division is central to life. The last stage, when two daughter cells split from each other, has fascinated scientists since the dawn of cell biology in the Victorian era. ...

A new method simplifies the analysis of RNA structure

1 hour ago

To understand the function of an RNA molecule, similar to the better-known DNA and vital for cell metabolism, we need to know its three-dimensional structure. Unfortunately, establishing the shape of an RNA ...

User comments : 0

Please sign in to add a comment. Registration is free, and takes less than a minute. Read more

Click here to reset your password.
Sign in to get notified via email when new comments are made.