Scientists say they have identified a critical mechanism that allows deadly bacteria to gain resistance to antibiotics. The findings, “The pentapeptide-repeat protein, MfpA, interacts with mycobacterial DNA gyrase as a DNA T-segment mimic”, which are published in Proceedings of the National Academy of Sciences (PNAS), offer a potential new drug target in the search for effective new antibiotics as we face the growing threat of antimicrobial resistance (AMR) and infections caused by bacterial pathogens.

The study investigated quinolone antibiotics which are used to treat a range of bacterial infections, including tuberculosis (TB). Quinolones work by inhibiting bacterial enzymes gyrase and topoisomerase IV, thereby preventing DNA replication and RNA synthesis essential to growth. They are highly-successful antimicrobial agents widely used in current medicine, but bacterial resistance to them and other treatments is a serious problem.

Previous studies had identified one resistance mechanism caused by the production of pentapeptide repeat proteins (PRPs), a family of molecules that also act as DNA gyrase inhibitors. One of these, called MfpA, confers quinolone resistance to Mycobacterium tuberculosis, the causative agent of TB.

“DNA gyrase, a type II topoisomerase, introduces negative supercoils into DNA using ATP hydrolysis. The highly effective gyrase-targeted drugs, fluoroquinolones (FQs), interrupt gyrase by stabilizing a DNA-cleavage complex, a transient intermediate in the supercoiling cycle, leading to double-stranded DNA breaks. MfpA, a pentapeptide-repeat protein in mycobacteria, protects gyrase from FQs, but its molecular mechanism remains unknown,” write the investigators.

“Here, we show that Mycobacterium smegmatis MfpA (MsMfpA) inhibits negative supercoiling by M. smegmatis gyrase (Msgyrase) in the absence of FQs, while in their presence, MsMfpA decreases FQ-induced DNA cleavage, protecting the enzyme from these drugs. MsMfpA stimulates the ATPase activity of Msgyrase by directly interacting with the ATPase domain (MsGyrB47), which was confirmed through X-ray crystallography of the MsMfpA–MsGyrB47 complex, and mutational analysis, demonstrating that MsMfpA mimics a T (transported) DNA segment.”

“These data reveal the molecular mechanism whereby MfpA modulates the activity of gyrase and may provide a general molecular basis for the action of other pentapeptide-repeat proteins.”

In this study John Innes Centre researchers in the group of Tony Maxwell, PhD, set out to discover how PRPs such as MfpA, work at the molecular level. They purified MfpA from Mycobacterium smegmatis, a close relative of M. tuberculosis, and showed that it can inhibit the supercoiling reaction of DNA gyrase, the target of quinolones in TB causing mycobacteria.

Further investigations showed that MfpA can prevent poisoning of gyrase by quinolones, thus protecting the bacterial host cell from the antibiotic.

Using X-ray crystallography, the team showed that MfpA binds to the ATPase domain of gyrase, and that this explains its ability to both inhibit the supercoiling reaction and prevent quinolone poisoning.

“We did not expect the exact mechanism of MfpA to be the prevention of DNA binding to the gyrase ATPase domain; this is a unique mode of action,” said Maxwell, corresponding author of the study. “We believe this understanding will help drive new ideas for antibiotic development among academics and researchers in the pharma industry.”

Further investigative work will involve molecular modeling based on the MfpA-gyrase structure to design small molecules that could mimic this interaction and offer more insights into how it works.

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