
AI antibiotics for superbugs could lead to ‘golden age of discovery'
AI virtually invented more than 50 million compounds and investigated whether they could kill MRSA and gonorrhoea, two of the most common superbugs.
More than 52,000 people a year in the UK catch antibiotic-resistant infections, which cause around 2,000 deaths annually.
Antimicrobial resistance, which creates superbugs, has been called the 'silent pandemic' and the problem of antibiotic resistance is set to get worse.
These deadly infections occur when a bacteria is treated with a drug but works out ways of neutralising the medicine.
The genetic protections make drugs less effective and can make common infections lethal.
Researchers at the Massachusetts Institute of Technology (MIT) used AI to come up with completely new ways of targeting these pathogens in the hope of making a breakthrough against superbugs.
'We're excited because we show that generative AI can be used to design completely new antibiotics,' Prof James Collins, the leader of the project at MIT, told the BBC.
'AI can enable us to come up with molecules, cheaply and quickly and in this way, expand our arsenal, and really give us a leg up in the battle of our wits against the genes of superbugs.'
AI was used to make as many hypothetical chemical compounds as possible that could target and kill the two bacterial infections.
The algorithms then filtered the results to show only those that worked in a novel way, had strong antimicrobial properties and were not toxic. This left one million possible new antibiotics in the virtual database.
Dr Aartia Krishnan, a postdoctoral researcher at MIT, said this step was key because the team's goal was to find drugs that worked in a completely different way to anything else ever used by doctors.
Scientists then tried to physically make around 170 of the most promising compounds. Only 24 of the chemicals could be created in a lab, with two for gonorrhoea and 22 against MRSA.
Tests in cells and mice found one of the novel gonorrhoea antibiotics and one of the MRSA compounds were able to kill bacteria.
'Both compounds exhibited mechanisms of action distinct from those of often-used antibiotics and were effective in reducing bacterial titers in different animal models of infection,' the study authors wrote in their paper, published in Cell.
'Additionally, both compounds exhibited a structure-activity landscape that can be productively used for further optimisation.
'Together, our results enable the generative design of two unique structural classes of antibacterial compounds and demonstrate the ability of our platform to explore uncharted regions of chemical space.'
A company affiliated with the MIT research project is now investigating if the two antibiotics, dubbed NG1 and DNA1, can be adapted for preclinical trials.
'We are exploring analogues, as well as working on advancing the best candidates preclinically, through medicinal chemistry work,' said Prof Collins.
'We are also excited about applying the platforms that Aarti and the team have developed toward other bacterial pathogens of interest, notably Mycobacterium tuberculosis and Pseudomonas aeruginosa.'
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