Cynthia Whitchurch

Last updated

Cynthia Whitchurch
NationalityAustralian
Alma mater University of Queensland, University of California, San Francisco
Awards David Syme Research Prize (2019) [1]
Scientific career
Fields Extracellular DNA (eDNA), bacteria, biofilms
Institutions Monash University, University of Technology Sydney, Quadram Institute
External videos
Nuvola apps kaboodle.svg “Professor Cynthia Whitchurch FAA”, Australian Academy of Science, 27 May 2019
Nuvola apps kaboodle.svg Welcome to the Data Arena, Fairfax Media, 12 April 2016

Cynthia B. Whitchurch FAA is an Australian microbiologist. Whitchurch is a research group leader at the Quadram Institute on the Norwich Research Park in the United Kingdom and was previously the founding director of the Microbial Imaging Facility and a Research Group Leader in the Institute of Infection, Immunity and Innovation (The ithree institute) at the University of Technology Sydney (UTS) in New South Wales. [2]

Contents

Whitchurch studies bacteria and the ways in which their behavior coordinates to form biofilms, an area with importance for the treatment of infection and the use of antibiotics. [1] [3] Whitchurch became a fellow of the Australian Academy of Science in 2019, [4] in recognition of her discovery that DNA plays a novel role in nature that is unrelated to its roles in genetic functioning. [5] [6] Whitchurch determined that extracellular DNA (eDNA) is essential to and promotes the self-organization of biofilms. [5] This information is credited with creating a paradigm shift in the understanding of biofilm biology. [5]

Education

Whitchurch attended the University of Queensland, where she completed a B. Sc. with Honors in 1989 and her PhD in 1994. [7] She then continued with postdoctoral training at the University of Queensland from 1995 to 2001. In 2001 Whitchurch undertook further training at the University of California, San Francisco, returning to Australia in 2004. [8] [9]

Career

In 2004, Whitchurch established her own research group in the Department of Microbiology at Monash University. University of Technology Sydney recruited Whitchurch in 2008; there she leads a research team that is part of the Institute of Infection, Immunity and Innovation (The ithree institute). [10] The team is investigating bacterial lifestyles looking at their connections to infection and antibiotic resistance. Whitchurch established and is the Director of the Microbial Imaging Facility at UTS. [11] In 2019, Whitchurch moved from Australia to join the Quadram Institute in the United Kingdom. [12] Whitchurch's group at the Quadram Institute researches how bacterial communities build biofilms and produce shared resources such as extracellular DNA, moonlighting proteins and membrane vesicles. [13]

Research

Whitchurch contributed to the discovery of novel roles for DNA unrelated to its genetic function, including the discovery in 2002 that extracellular DNA (eDNA) is required for building multicellular bacterial communities known as biofilms. [5] [6] Whitchurch's discovery that extracellular DNA (eDNA) is essential to and promotes the self-organization of biofilms is credited with creating a paradigm shift in the understanding of biofilm biology. [5]

One of the bacteria that Whitchurch studies is Pseudomonas aeruginosa , a common bacterium which has developed a dangerous antibiotic-resistant strain or superbug. P. aeruginosa thrives on implanted devices such as catheters, and is a significant cause of hospital-acquired infections. [3] P. aeruginosa also forms potentially life-threatening biofilms in the lungs of cystic fibrosis patients. [14]

In addition to using sophisticated microscopes, Whitchurch and her team have developed computer programs to analyze data to segment, identify, track and analyse the movements of bacterial cells. They have used the UTS "data arena" to create interactive 360-degree 3-dimensional computational displays representing the behavior of bacterial cells. Colour-coding cells according to the speed at which they move, and studying the ways in which bacteria move across surfaces, helps Whitchurch to visualize behaviors in new ways. Recognizing that P. aeruginosa tends to create and follow pathways (a process known as stigmergy [1] ) has led her to experiment with the use of furrowed surfaces in catheters. This appears to disrupt the movement of the bacteria and may help to prevent infection. [3] [15]

Round cells are viable until explosive cell lysis of P. aeruginosa

In 2016, Whitchurch, Lynne Turnbull and other researchers from Australia, Japan and Switzerland discovered that the bacterium P. aeruginosa can actively explode, widely distributing its contents when it dies. Its protein, DNA, and virulence factors then become available to other bacterium and support the formation of increasingly dangerous biofilms. A particular gene appears to support both this explosive cell lysis and the formation of biofilms. This suggests possibilities for treatment. [16] [17]

"The normal bacteria look like little rods or pills," says Whitchurch. "One day, as we looked under the microscope, we saw one of the cells turn from a hard, structured rod into a round, soft ball. Within a few more seconds, it then violently exploded - it's amazing how quickly it happens and is likely the reason it hasn't been observed before." [16]

Awards and recognition

Whitchurch received the R Douglas Wright Career Development Award (2004-2008) from the National Health and Medical Research Council. [18] In 2009 she was awarded an NHMRC Senior Research Fellowship. [19]

In 2017 Whitchurch was awarded the David Syme Research Prize, an award recognizing "the best original research in biology, physics, chemistry or geology, produced in Australia during the preceding two years". She was the first woman in more than 30 years to receive the prize. [1]

In 2019 Whitchurch was elected to the Australian Academy of Science. [5]

Media

Whitchurch's research on biofilms was featured by the Australian Broadcasting Corporation in 2002 [14] and 2013 [20] and The Australian in 2019. [21]

Related Research Articles

<span class="mw-page-title-main">Bacteriophage</span> Virus that infects and replicates within bacteria

A bacteriophage, also known informally as a phage, is a virus that infects and replicates within bacteria and archaea. The term was derived from "bacteria" and the Greek φαγεῖν, meaning "to devour". Bacteriophages are composed of proteins that encapsulate a DNA or RNA genome, and may have structures that are either simple or elaborate. Their genomes may encode as few as four genes and as many as hundreds of genes. Phages replicate within the bacterium following the injection of their genome into its cytoplasm.

<span class="mw-page-title-main">Biofilm</span> Aggregation of bacteria or cells on a surface

A biofilm is an syntrophic community of microorganisms in which cells stick to each other and often also to a surface. These adherent cells become embedded within a slimy extracellular matrix that is composed of extracellular polymeric substances (EPSs). The cells within the biofilm produce the EPS components, which are typically a polymeric combination of extracellular polysaccharides, proteins, lipids and DNA. Because they have three-dimensional structure and represent a community lifestyle for microorganisms, they have been metaphorically described as "cities for microbes".

<span class="mw-page-title-main">Phage therapy</span> Therapeutic use of bacteriophages to treat bacterial infections

Phage therapy, viral phage therapy, or phagotherapy is the therapeutic use of bacteriophages for the treatment of pathogenic bacterial infections. This therapeutic approach emerged at the beginning of the 20th century but was progressively replaced by the use of antibiotics in most parts of the world after the Second World War. Bacteriophages, known as phages, are a form of virus that attach to bacterial cells and inject their genome into the cell. The bacteria's production of the viral genome interferes with its ability to function, halting the bacterial infection. The bacterial cell causing the infection is unable to reproduce and instead produces additional phages. Phages are very selective in the strains of bacteria they are effective against.

A slime layer in bacteria is an easily removable, unorganized layer of extracellular material that surrounds bacteria cells. Specifically, this consists mostly of exopolysaccharides, glycoproteins, and glycolipids. Therefore, the slime layer is considered as a subset of glycocalyx.

<i>Pseudomonas aeruginosa</i> Species of bacterium

Pseudomonas aeruginosa is a common encapsulated, Gram-negative, aerobic–facultatively anaerobic, rod-shaped bacterium that can cause disease in plants and animals, including humans. A species of considerable medical importance, P. aeruginosa is a multidrug resistant pathogen recognized for its ubiquity, its intrinsically advanced antibiotic resistance mechanisms, and its association with serious illnesses – hospital-acquired infections such as ventilator-associated pneumonia and various sepsis syndromes. P. aeruginosa is able to selectively inhibit various antibiotics from penetrating its outer membrane - and has high resistance to several antibiotics, according to the World Health Organization P. aeruginosa poses one of the greatest threats to humans in terms of antibiotic resistance.

<span class="mw-page-title-main">Extracellular polymeric substance</span> Gluey polymers secreted by microorganisms to form biofilms

Extracellular polymeric substances (EPSs) are natural polymers of high molecular weight secreted by microorganisms into their environment. EPSs establish the functional and structural integrity of biofilms, and are considered the fundamental component that determines the physicochemical properties of a biofilm. EPS in the matrix of biofilms provides compositional support and protection of microbial communities from the harsh environments. Components of EPS can be of different classes of polysaccharides, lipids, nucleic acids, proteins, lipopolysaccharides, and minerals.

Autoinducers are signaling molecules that are produced in response to changes in cell-population density. As the density of quorum sensing bacterial cells increases so does the concentration of the autoinducer. Detection of signal molecules by bacteria acts as stimulation which leads to altered gene expression once the minimal threshold is reached. Quorum sensing is a phenomenon that allows both Gram-negative and Gram-positive bacteria to sense one another and to regulate a wide variety of physiological activities. Such activities include symbiosis, virulence, motility, antibiotic production, and biofilm formation. Autoinducers come in a number of different forms depending on the species, but the effect that they have is similar in many cases. Autoinducers allow bacteria to communicate both within and between different species. This communication alters gene expression and allows bacteria to mount coordinated responses to their environments, in a manner that is comparable to behavior and signaling in higher organisms. Not surprisingly, it has been suggested that quorum sensing may have been an important evolutionary milestone that ultimately gave rise to multicellular life forms.

Roberto Kolter is Professor of Microbiology, Emeritus at Harvard Medical School, an author, and past president of the American Society for Microbiology. Kolter has been a professor at Harvard Medical School since 1983 and was Co-director of Harvard's Microbial Sciences Initiative from 2003-2018. During the 35-year term of the Kolter laboratory from 1983 to 2018, more than 130 graduate student and postdoctoral trainees explored an eclectic mix of topics gravitating around the study of microbes. Kolter is a fellow of the American Association for the Advancement of Science and of the American Academy of Microbiology.

Sharklet, manufactured by Sharklet Technologies, is a bio-inspired plastic sheet product structured to impede microorganism growth, particularly bacterial growth. It is marketed for use in hospitals and other places with a relatively high potential for bacteria to spread and cause infections. Coating surfaces with Sharklet works due to the nano-scale texture of the product's surface.

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Urs Jenal is a Swiss Microbiologist and Professor at the Biozentrum University of Basel, Switzerland.

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<span class="mw-page-title-main">Center for Biofilm Engineering</span>

The Center for Biofilm Engineering (CBE) is an interdisciplinary research, education, and technology transfer institution located on the central campus of Montana State University in Bozeman, Montana. The center was founded in April 1990 as the Center for Interfacial Microbial Process Engineering with a grant from the Engineering Research Centers (ERC) program of the National Science Foundation (NSF). The CBE integrates faculty from multiple university departments to lead multidisciplinary research teams—including graduate and undergraduate students—to advance fundamental biofilm knowledge, develop beneficial uses for microbial biofilms, and find solutions to industrially relevant biofilm problems. The center tackles biofilm issues including chronic wounds, bioremediation, and microbial corrosion through cross-disciplinary research and education among engineers, microbiologists and industry.

Everett Peter Greenberg is an American microbiologist. He is the inaugural Eugene and Martha Nester Professor of Microbiology at the Department of Microbiology of the University of Washington School of Medicine. He is best known for his research on quorum sensing, and has received multiple awards for his work.

<span class="mw-page-title-main">Twitching motility</span> Form of crawling bacterial motility

Twitching motility is a form of crawling bacterial motility used to move over surfaces. Twitching is mediated by the activity of hair-like filaments called type IV pili which extend from the cell's exterior, bind to surrounding solid substrates, and retract, pulling the cell forwards in a manner similar to the action of a grappling hook. The name twitching motility is derived from the characteristic jerky and irregular motions of individual cells when viewed under the microscope. It has been observed in many bacterial species, but is most well studied in Pseudomonas aeruginosa, Neisseria gonorrhoeae and Myxococcus xanthus. Active movement mediated by the twitching system has been shown to be an important component of the pathogenic mechanisms of several species.

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References

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  2. "Cynthia Whitchurch". University of Technology Sydney. Retrieved 25 July 2019.
  3. 1 2 3 Alexander, Harriet (12 April 2016). "How visualising data helped UTS microbiologist Cynthia Whitchurch in her attempt to defeat a superbug". The Sydney Morning Herald. Retrieved 23 August 2019.
  4. 1 2 3 4 5 6 "Professor Cynthia Whitchurch". Australian Academy of Science. Retrieved 25 July 2019.
  5. 1 2 Whitchurch, C. B. (22 February 2002). "Extracellular DNA Required for Bacterial Biofilm Formation". Science. 295 (5559): 1487. doi:10.1126/science.295.5559.1487. PMID   11859186.
  6. "PROFESSOR CYNTHIA WHITCHURCH". ARC Training Centre for Innovative Engineering University of Sydney. Retrieved 23 August 2019.
  7. "Professor Cynthia Whitchurch". Australian Research Council Training Centre for Innovative BioEngineering. Retrieved 20 August 2019.
  8. "Cynthia Whitchurch | B Sc (HonsI); PhD | University of Technology Sydney, Sydney | UTS | The ithree Institute | ResearchGate". ResearchGate. Retrieved 20 August 2019.
  9. "Who we are". University of Technology Sydney. Archived from the original on 25 July 2019. Retrieved 12 August 2021.
  10. "About us". University of Technology Sydney. 17 May 2019. Retrieved 25 July 2019.
  11. "QI welcomes Cynthia Whitchurch". Quadram Institute. 9 October 2019. Archived from the original on 2 March 2021. Retrieved 12 August 2021.
  12. "Cynthia Whitchurch". Quadram Institute. Retrieved 12 August 2021.
  13. 1 2 "Bacterial slime buster". Australian Broadcasting Corporation . 22 February 2002. Retrieved 25 July 2019.
  14. 1 2 Bowler, Jacinta (28 April 2016). "Some Superbugs Literally Explode When They Die, Making Them Even More Deadly". Science Alerts. Retrieved 24 August 2019.
  15. "University of Technology Sydney". web-tools.uts.edu.au. Retrieved 20 August 2019.
  16. "Associate Professor Cynthia Whitchurch". Research Data Australia. Retrieved 20 August 2019.
  17. Salleh, Anna (25 June 2013). "Secrets of trail-blazing bacteria revealed". Australian Broadcasting Corporation . Retrieved 25 July 2019.
  18. "Cynthia Whitchurch's starring role in bacteria fight worth an academy award". The Australian. 29 May 2019. Retrieved 25 July 2019.