By Nick Lavars May 04, 2021
The superbug Pseudomonas aeruginosa, after being “popped like a balloon”Imperial College London.
By turning modern scientific tools on an antibiotic discovered 70 years ago, researchers have unearthed a previously unknown mechanism it uses to pierce and pop superbugs like balloons. Promisingly, the scientists have also demonstrated how this approach to taking out bacteria can be supercharged by combining it with other antibiotics, potentially offering a new form of defense against deadly, drug-resistant bacteria.
The drug at the center of this study is called colistin, which was first described in 1947 and has since become a last-resort treatment for bacterial infections that have grown resistant to other medications. As one of only a handful of drugs capable of taking the fight to the deadliest of superbugs, such as E. Coli, Pseudomonas aeruginosa and Acinetobacter baumannii, colistin works by puncturing the two membranes encasing the bacteria. Though how it does this has been unclear.
Scientists knew that the drug can penetrate the outer membrane by zeroing in on a target chemical called lipopolysaccharide (LPS). The trouble was, there is very little of this chemical to be found in the inner membrane, raising questions over how colistin is able to find and punch its way through.
“It sounds obvious that colistin would damage both membranes in the same way, but it was always assumed colistin damaged the two membranes in different ways,” says Imperial College London’s Dr Andrew Edwards, who led the research. “There’s so little LPS in the inner membrane that it just didn’t seem possible, and we were very skeptical at first. However, by changing the amount of LPS in the inner membrane in the laboratory, and also by chemically modifying it, we were able to show that colistin really does puncture both bacterial skins in the same way – and that this kills the superbug.”
The superbug Pseudomonas aeruginosa, prior to being “popped like a balloon” in new superbug researchImperial College London
With this new understanding of the way colistin functions, the team continued to investigate ways to enhance its bacteria-killing abilities. This involved experiments on the bacterium Pseudomonas aeruginosa, in which the scientists found that an experimental antibiotic called murepavadin could be used to drive up levels of LPS in its inner skin. This in turn enabled colistin to far more easily penetrate and kill the bug.
While decades old, colistin finds itself growing only more important as drug-resistant bacteria continues evolve and pose a greater threat to human life. In fact, the World Health Organization has designated it as one of the “Highest Priority Critically Important Antimicrobials,” for its role as a last-ditch medication in critically ill patients, and we’re seeing a lot of research into how we might shore up its defenses.
“As the global crisis of antibiotic resistance continues to accelerate, colistin is becoming more and more important as the very last option to save the lives of patients infected with superbugs,” says Akshay Sabnis, lead author of the work. “By revealing how this old antibiotic works, we could come up with new ways to make it kill bacteria even more effectively, boosting our arsenal of weapons against the world’s superbugs.”
The research was published in the journal eLife.
Source: Imperial College London
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