How old compounds could become tomorrow's life-savers

February 6, 2018, University of Leeds
How old compounds could become tomorrow’s life-savers
Credit: University of Leeds

University of Leeds scientists are looking back in time at previously discarded chemical compounds, to see if any could be developed for new antibiotics.

In the heyday of antibiotic development in the mid-20th century, many different with were examined, but only a small proportion were selected for development into drugs.

But with modern-day diseases becoming increasingly resistant to those drugs, biological scientists and chemists at Leeds are now re-examining old , applying advances in science and technology to test more precisely whether they could still hold the key to a future medicine.

Dr. Alex O'Neill, from the Antimicrobial Research Centre at the University, said: "We're showing the value of reviewing compounds previously put on the back of the shelf. Amongst the 3,000 or so antibiotics discovered to date, only a handful have been brought into clinical use. There may be a wealth of compounds out there with untapped potential.

"At the moment, the bugs are outsmarting the scientists, and we can't allow that to continue. By studying compounds which past research has shown already have antibacterial properties, there is scope for a potential fast-track through the challenging early stages of discovery. This approach could pave the way for life-saving new drugs."

Potential for new drug

Dr. O'Neill's latest research found that a compound identified in the 1940s could now be a realistic contender as the basis of a new antibiotic drug.

A family of compounds, known as the actinorhodins, was originally identified as having weak antibiotic properties, but was not taken forward for development into a drug.

However, Dr. O'Neill said that at the time scientists did not fully differentiate the individual compounds within the family when they examined them, leading to a less than precise picture of their properties.

This prompted his team to divide the family and select a specific compound (y-ACT) for further evaluation, using an array of 21st century approaches, to assess its potential and to understand how it works against bacteria.

Serious contender

Dr. O'Neill and colleague Professor Chris Rayner from the University's School of Chemistry have published their findings in the journal Scientific Reports, and believe the compound is worth serious consideration as the basis for a new drug to combat certain types of bacterial infections.

Dr. O'Neill added: "y-ACT exhibits potent antibacterial activity against two important representatives of the ESKAPE class of pathogens, which are bacteria that have developed the ability to 'escape' the action of existing drugs.

"A major challenge in tackling the problem of antibiotic resistance is to discover new drugs – our study shows that potentially useful drug candidates can be 'discovered' from amongst the antibiotics we already know about.

"The weak activity previously published for the ACT family as a whole probably explains why this group was not further evaluated, and it is intriguing to think that other potentially useful antibiotic groups are languishing in obscurity in academic journals just needing expert review using modern processes and equipment."

Urgent need

Supporting Dr. O'Neill's work, Dr. Jonathan Pearce, Head of Infections and Immunity at the Medical Research Council, said: "There is an urgent need to discover new ways to fight AMR and the scientific community is leaving no stone unturned in its search for . This includes revisiting chemical compounds that were once shelved.

"Until recently, no new antibiotics had been discovered for 25 years. Dr. O'Neill's research is important: it's providing another way of looking for potential antibiotics and could hold the key to uncovering options that were overlooked before but may be incredibly useful now."

Stopping E.coli

Also based in Leeds' School of Chemistry is Dr. Michael Webb, whose research focuses on a compound, called pentyl pantothenamide, first assessed in the 1970s.

Then, it was found to be able to stop the growth of E.coli but not completely kill the bacteria, so was never taken into clinical use.

At the time, scientists did not understand how it was able to stop the growth, but Dr. Webb and his team have proved it is driven by Vitamin B5, which is used to metabolise energy. Bacteria have to make B5 and a key part of the machinery they use to do so is called the PanDZ complex.

Pentyl pantothenamide targets the PanDZ complex, preventing E. coli from making Vitamin B5 and so starving it of the means to grow.

Dr. Webb said: "The results of our latest studyopen up the possibility of designing that use the same means to attack E. coli, but in a more effective way."

Dr. O'Neill concludes: "Our findings underscore the importance of revisiting unexploited as a potential source of new antibiotic drug candidates. We now believe a comprehensive re-evaluation of such compounds is worthwhile, potentially offering new ways to protect against infections."

Explore further: Research points to second chance for rejected antibiotic candidate

More information: Nada M. Nass et al. Revisiting unexploited antibiotics in search of new antibacterial drug candidates: the case of γ-actinorhodin, Scientific Reports (2017). DOI: 10.1038/s41598-017-17232-1

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