A team of cross-institutional University of Queensland researchers led by Professor Matt Sweet, Professor Mark Schembri and Dr Ronan Kapetanovic examined how our immune system uses zinc to fight uropathogenic Escherichia coli (UPEC) - the major cause of UTIs.
Dr Kapetanovic, from UQ's Institute for Molecular Bioscience (IMB), said researchers already knew that zinc was toxic to bacteria.
They also discovered that UPEC has a two-pronged strategy to survive the body's immune response.
"We found that, compared to non-pathogenic bacteria, UPEC can evade the zinc toxicity response of macrophages, but these bacteria also show enhanced resistance to the toxic effects of the zinc.
"These findings give us clues to how our immune system battles infections, and also potential avenues to develop treatments, such as blocking UPEC's escape from zinc to make it more sensitive to this metal.
"Treatment strategies that don't use antibiotics have the advantage of bacteria not developing resistance; if we can reprogram our immune cells to make them stronger, or change the way they respond to bacteria, we would be better equipped to fight superbugs."
UQ's School of Chemistry and Molecular Biosciences Dr Minh Duy Phan said the study also identified the full set of UPEC genes that provide protection against zinc toxicity.
"This knowledge provides another potential avenue for developing antimicrobial agents for the treatment of UTIs", Dr Phan said.
IMB PhD student Miss Claudia Stocks said the methods the team used could be applied to the study of other bacterial diseases, not just UTIs.
"Macrophages deploy zinc toxicity against several types of bacteria, such as Mycobacterium tuberculosis, Salmonella and Streptococcus, that aren't necessarily being cleared from the body by normal mechanisms," Miss Stocks said.
"We developed zinc sensors that can be adapted to study different types of bacteria, bringing us closer to understanding our immune system better and creating therapies for a range of infectious diseases."
The research was published in Proceedings of the National Academy of Sciences USA and funded by Australia's National Health and Medical Research Council, the Australian Research Counciland Australian Cancer Research Foundation.
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