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[Music. Woman talks to camera.]

I'm Cynthia Whitchurch I'm a professor here at UTS. My area of research is microbiology. So I'm intrigued by understanding bacteria and how they behave, how do they coordinate their activities.

What's kept me fascinated is trying to understand how what we think of just as really simple single-celled organisms, how do they actually behave in these really complex ways.

When I joined UTS, I established the Microbial Imaging Facility. We can visualise subcellular structures of bacteria using these super resolution microscopy techniques, and it's just an amazing time to be a microbiologist, actually.

The major contributions that I've had scientifically is demonstrating that bacteria release extracellular DNA and when DNA is outside of the cell, it can have functions that have got nothing to do with genetic coding.

And so when it’s outside of the cell, it actually functions as a glue, and it is used as a glue to hold these bacterial communities together. So I demonstrated it had a function and now from there it's been shown to be a ubiquitous process – lots of other microorganisms use DNA as a glue.

And what's really cool about that is that there's an enzyme that cystic fibrosis patients use to help clear that their mucus load, called pulmosyme, but it's actually an enzyme that breaks up DNA. So it's now used in some countries prophylactically in an attempt to reduce the rate of infection of CF patients.

Where I'm really excited about where we're heading now is in this drug discovery project that we've got going where we're exploring the bacterial lifestyle transition, when they get exposed to penicillin antibiotics we find that they're susceptible to other things. And I think that there's a lot of prospect in there to actually go in and maybe come up with new ways of dealing with antimicrobial resistance. I think we need some smart approaches to help combat that, and maybe we can contribute to that.

Those breakthroughs are worth it every time.

[Music]

Professor Cynthia Whitchurch has spent her academic life trying to truly understand one of the simplest forms of life on Earth, bacteria, with the aim of exploiting her findings to develop innovative ways to control infections.

Her work has important implications. Understanding how bacteria behave is key to controlling their spread and fighting the rise of antibiotic-resistant strains, says Whitchurch, the founding director of the Microbial Imaging Facility at UTS.

It is work that is also paying dividends with Whitchurch’s discoveries now being embraced by the medical implants industry with outstanding success.

One company has noted a 50 per cent reduction in infection rates – and a $10 million saving in revision treatment – after design changes, informed by Whitchurch’s work, were made to its implantable device.

Her team is also working with a Sydney-based company to limit infections from catheters, one of the most common sources of hospital-acquired infections.

A key discovery underpinning this collaboration is Whitchurch’s revelation that bacterial communities – known as biofilms – follow pathways reinforced by continual use. It’s the same principle that underpins the movement of ants, traffic and even the internet.

Critical in helping Whitchurch visualise and better understand the collective movement of bacteria was the UTS Data Arena, which allowed her to interact in 3D with the bacteria as they moved across a surface.

“We were able to easily see in the whole biofilm where cells were moving fast. That revealed behaviours we really couldn't have appreciated in any other way,” she says.

We were able to easily see in the whole biofilm where cells were moving fast. That revealed behaviours we really couldn't have appreciated in any other way.

— Professor Cynthia Whitchurch, founding director, UTS Microbial Imaging Facility

Having identified these patterns, Whitchurch looked for ways to exert what she calls ‘mind control’ over the bacteria’s behaviour.

“In the lab, we’ve made some two-dimensional surfaces where we put a parallel series of furrows in the way of the bacteria,” she explains.

“When they hit that surface, they end up running up and down these furrows, which slows their overall migration rate. So they’re going where we want them to go instead of where they want to go.”

In an era of multi-drug-resistant superbugs, this groundbreaking work will grow in relevance as advances in medical technology and an ageing population will see an increased use of medical devices such as cardiac pacemakers, artificial joint replacements, prosthetic heart valves and catheters.

A halving of infection rates from implant surgeries – an outcome already proven by her work – has the potential to dramatically cut healthcare costs and risks associated with replacement devices. 

This work also builds on another significant discovery in which Whitchurch demonstrated that individual bacterial cells can ‘altruistically’ explode, releasing DNA that their fellow bacteria then use to build biofilms and continue the spread of infection.

“We’ve discovered that the extracellular DNA released through exploding cells is very important in enabling the remaining bacteria to coordinate their behaviours … and be really highly organised when they’re running through this furrow network,” she says. “It even enables them to build those furrows, because they use it to glue themselves together to combine enough power to be able to gouge out the furrows.”

These findings are the linchpins in a body of work that is influencing further discoveries internationally with her 2002 Science paper, which showed for the first time that extracellular DNA is required for biofilm formation, one of the most cited in its field. 

In 2017, Whitchurch became the first woman in 30 years to be awarded the David Syme Research Prize.

Research team

  • Professor, ithree Institute
  • Professor, School of Mathematical and Physical Sciences
  • Ben Simons
    Ben Simons
    Technical Director, UTS Data Arena, eResearch Support

Additional team members

Michelle Gee, University of Melbourne
Scott Wade, Swinburne University of Technology

Research centre

 

Funded by

  • Australian Research Council
  • National Health and Medical Research Council

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