MONASH (AUS) — In the fight against antibiotic resistance, the next strategy may be to disarm the bacteria without actually killing them.
Published in Nature Structure and Molecular Biology, research led by Monash University shows a protein complex called the Translocation and Assembly Module (TAM), forms a type of molecular pump in bacteria.
The TAM allows bacteria to shuttle key disease-causing molecules from inside the bacterial cell where they are made, to the outside surface, priming the bacteria for infection.
Lead author and PhD student Joel Selkrig of the department of biochemistry and molecular biology says the work paves the way for future studies to design new drugs that inhibit this process.
“The TAM was discovered in many disease-causing bacteria, from micro-organisms that cause whooping cough and meningitis, to hospital-acquired bacteria that are developing resistance to current antibiotics,” says Selkrig.
“It is a good antibacterial target because a drug designed to inhibit TAM function would unlikely kill bacteria, but simply deprive them of their molecular weaponry, and in doing so, disable the disease process.”
“By allowing bacteria to stay alive after antibiotic treatment, we believe we can also prevent the emergence of antibiotic resistance, which is fast becoming a major problem worldwide.”
The Monash team, led by Professor Trevor Lithgow, shows the TAM was made of two protein parts, TamA and TamB, which function together to form a machine of molecular scale.
Together with colleagues at the University of Melbourne, they compared normal virulent bacteria to mutant strains of bacteria engineered to have no TAM.
“We noticed that proteins important for disease were missing in the outer membrane of the mutant bacteria,” Selkrig says. “The absent proteins help bacteria to adhere to our bodies and perform disease-related functions.”
Selkrig says the next step for the group was to dissect the molecular mechanism of how the TAM complex functions and, in collaboration with researchers at the Monash Institute of Pharmaceutical Sciences, design an antibiotic that inhibits the TAM in bacteria.
Lithgow led an international team of seven Monash researchers, and scientists from the University of Melbourne, University of Queensland, the University of Glasgow, and University of Birmingham.
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