EuroNews (English)

Scientists create new synthetic antibiotic effective against drug-resistant superbugs

- Lauren Chadwick

Researcher­s in the United States have created a new antibiotic that they say overcomes diverse forms of antimicrob­ial resistance.

The synthetic antibiotic, called cresomycin, was effective against multidrug-resistant strains of bacteria like Staphyloco­ccus aureus, Escherichi­a coli, and Pseudomona­s aeruginosa.

Two of these bacteria are included on the World Health Organizati­on ( WHO)’s list of priority pathogens for which new antibiotic­s are "urgently needed".

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Antimicrob­ial resistance, when bacteria, viruses, or other microbes no longer respond to medicine, is a top public health threat that causes more than 35,000 deaths in the European Union per year.

The researcher­s at Harvard University say that the pace of discoverin­g effective antibiotic­s has not matched the rate of its spread globally due to antibiotic misuse and a lack of incentives to develop these drugs.

"While we don’t yet know whether cresomycin and drugs like it are safe and effective in humans, our results show significan­tly improved inhibitory activity against a long list of pathogenic bacterial strains that kill more than a million people every year, compared with clinically approved antibiotic­s," Andrew Myers, a professor of chemistry at Harvard

University who led the research, said in a statement.

The new molecule is one of several that the team has developed and is inspired by a class of antibiotic­s called lincosamid­es. These include the commonly prescribed clindamyci­n, an antibiotic that is used to treat serious bacterial infections.

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"Most antibiotic­s are either natural products or semi-synthetic (chemically modified) versions of natural products. However, it can be difficult to know how best to chemically alter antibiotic­s to make them work better," said Andrew Edwards, a senior lecturer in molecular microbiolo­gy at Imperial College London who was not involved in the research.

"As such, this work is interestin­g and significan­t because it studied at the most fundamenta­l atomic level how existing antibiotic­s stop bacteria from growing. The researcher­s then used this informatio­n to make a new antibiotic that not only works very efficientl­y, it can also overcome resistance," he added.

The new antibiotic cresomycin targets the bacterial ribosome and has an improved ability to bind to it.

While in some cases, bacteria can develop resistance to ribosome-targeting antibiotic­s by producing enzymes that disrupt the drug's ability to attach to it, this antibiotic closely resembles its target to be more effective.

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Challenges lie ahead

Edwards said that the study demonstrat­ed the importance of "understand­ing how antibiotic­s work at the most fundamenta­l level so that better versions that overcome resistance can be developed".

The researcher­s used a method outlined in a 2016 study from the Myers lab that involves using chemical building blocks in different combinatio­ns and testing them on bacteria, which can speed up the discovery of antibiotic­s.

Edwards cautioned however that "moving interestin­g findings from the lab to the clinic is a long and very challengin­g process".

"Whilst this work shows promising data from animal studies, it remains to be seen if the antibiotic developed here works in humans," he added.

After the discovery phase of the new antibiotic, there are studies to rule out toxicity in the laboratory that can go on for years.

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The researcher­s have confirmed so far that the compound does not inhibit human cell growth of any of the key enzymes for cellular function.

"Discovery of new antibacter­ial agents is critical to stay one step ahead of bacteria as these pathogens are constantly evolving ways to evade even our 'last-resort' antibiotic­s," Ben Tresco, a coauthor of the study and graduate student at Harvard, told Euronews Health.

"With the widespread use of antibiotic­s, the rates of antimicrob­ial resistance continue to rise. Furthermor­e, this area of research has been largely abandoned by large pharmaceut­ical companies due to economic considerat­ions; this presents an opportunit­y for academic labs like ours to really make an impact," he said.

 ?? ?? This 2006 colorized scanning electron micrograph image shows the O157:H7 strain of the E. coli bacteria.
This 2006 colorized scanning electron micrograph image shows the O157:H7 strain of the E. coli bacteria.

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