Dr Joe Latimer

Lecturer in Antimicrobial Resistance

  • Peel Building Room G11
  • T: +44 (0)161 295 0283
  • E: j.latimer2@salford.ac.uk
  • Twitter: @DrJoeLatimer

Office Times

Please contact me via e-mail for an appointment

Biography

I first studied at Lancaster University, which was a fantastic broad grounding in biological sciences. After a year of travelling moved to Manchester to take the MSc in Medical and Molecular Microbiology. The master’s inspired me to begin medical microbiology research and, luckily enough, I later lectured on the same course.

I then worked in London for a while, but missed the North. I moved to the department of Molecular Biology and Biotechnology in Sheffield, and studied for a PhD in biofilm physiology under Professor Robert Poole. I developed a chemostat model to grow biofilms for transcriptomic profiling and discovered that Escherichia coli forms biofilms more efficiently in the absence of oxygen.

After the PhD, I worked in Malawi with Ripple Africa, teaching biology, training teachers and helping out at the local rural hospital. This was a fantastic experience and I retain strong ties with the community in which I lived.

I returned to Manchester in 2009 and joined NeuTec Pharma, where I discovered a target for an antibody therapy candidate against Clostridium difficile. However, the call of academia was strong, and I came back to the University of Manchester in May 2010, originally conducting research in oral microbiology and antimicrobials with Andrew McBain in Manchester Pharmacy School. I supervised a small team developing models to investigate anti-biofilm and anti-bacterial effects of oral healthcare formulations - research that had a direct impact on the development of healthcare products.

I also pursued a side-project characterising the adaptation of Staphylococcus aureus to triclosan. This has so far yielded two well-received papers which highlighted the remarkable ability of bacteria to adapt to their surroundings.

In order to pursue my interests in host-microbe interactions, I chose a second postdoctoral position in 2015 with Dr Cath O’Neill investigating the roles of the skin microbiome in barrier disruption and inflammation. I developed a reproducible ex-vivo skin model to explore the complex interactions of our skin with our resident bacteria.

I moved to the University of Salford in 2016, where I plan to combine my interests in bacteria, biofilms, host-microbe interactions and antimicrobials. I want to enthuse a new generation of microbiologists in all things bacteria and instil a healthy respect for the promises and dangers of antimicrobial use!

Teaching

I teach across all levels in courses including the BSc (Hons) Human Biology & Infectious Diseases and the MSc in Biotechnology. I specialise in microbiology, vaccines, antimicrobials and antibiotic resistance

Research Interests

For millions of years, we have been evolving alongside a host of microbes that live on us, in us and which help us to survive. ‘We’ interact with ‘them’ constantly but we are only just starting to figure out what these interactions are and what they might mean.

My research focuses on characterising some of these interactions, looking at how bacteria adapt to life on Planet Human and how we, in turn, respond to these changes. I want to know what happens when these interactions are disturbed through injury and antibiotic use. I am also interested in how different microbes interact with each other on human tissues and the roles of biofilms in this process.

If we can dissect these complex relationships, we might hope to eventually develop much smarter ways to combat infection and antibiotic resistance.

Qualifications and Memberships

Qualifications

BSc (Hons) Biological Sciences, Lancaster University, 2000

MSc Medical and Molecular Microbiology, University of Manchester, 2003

PhD Molecular Biology of Biofilms, University of Sheffield, 2008

Memberships:

The Microbiology Society

American Society of Microbiology

European Society of Dermatological Research

Publications

2016

  • Forbes, S., Latimer, J., Sreenivasan, P. K., & Mcbain, A. (2016). Simultaneous Assessment of Acidogenesis-Mitigation and Specific Bacterial Growth-Inhibition by Dentifrices. PLoS One11(2).

2015

  • Latimer, J., Munday, J. L., Buzza, K. M., Sreenivasan, P. K., & McBain, A. J. (2015). Antibacterial efficacy of a cetylpyridinium chloride-based mouthrinse against Fusobacterium nucleatum and in vitro plaques. American Journal of Dentistry28 Spec No A.
  • Latimer, J., Forbes, S., Bazaid, A., & McBain, A. J. (2015). Altered Competitive Fitness, Antimicrobial Susceptibility, and Cellular Morphology in a Triclosan-Induced Small-Colony Variant of Staphylococcus aureus. Antimicrobial Agents and Chemotherapy59(8).
  • Latimer, J., Munday, J. L., Buzza, K. M., Forbes, S., Sreenivasan, P. K., & McBain, A. J. (2015). Antibacterial and anti-biofilm activity of mouthrinses containing cetylpyridinium chloride and sodium fluoride. BMC Microbiology15.

2014

  • Latimer, J., Munday, J. L., Buzza, K. M., & McBAIN, A. J. (2014). A Comparison of the Antibacterial Efficacy of Two Toothpaste Formulations Containing 0.3% Triclosan. J. Ind. Dent. Ass.2(8), 18-23.
  • Ledder, R. G., Latimer, J., Humphreys, G. J., Sreenivasan, P. K., & McBain, A. J. (2014).Bacteriological effects of dentifrices with and without active ingredients of natural origin. Applied and Environmental Microbiology80(20).

2013

  • Rattray, N. J. W., Zalloum, W. A., Mansell, D., Latimer, J., Jaffar, M., Bichenkova, E. V., & Freeman, S. (2013). Chemical and bacterial reduction of azo-probes: monitoring a conformational change using fluorescence spectroscopy. Tetrahedron69(13), 2758-2766.

2012

  • Rattray, N. J. W., Zalloum, W. A., Mansell, D., Latimer, J., Schwalbe, C. H., Blake, A. J., Freeman, S.(2012). Fluorescent probe for detection of bacteria: Conformational trigger upon bacterial reduction of an azo bridge. Chemical Communications48(51), 6393-6395.
  • Latimer, J., Forbes, S., & McBain, A. J. (2012). Attenuated virulence and biofilm formation in Staphylococcus aureus following sublethal exposure to triclosan. Antimicrobial Agents and Chemotherapy56(6), 3092-3100.

2009

  • Latimer, J., Stokes, S. L., Graham, A. I., Bunch, J., Jackson, R. J., McLeod, C. W., & Poole, R. K. (2009).A novel method for exploring elemental composition of microbial communities: laser ablation-inductively coupled plasma-mass spectrometry of intact bacterial colonies. Journal of Microbiological Methods79(3).