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George Salmond
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Molecular Microbiology: Bacterial Quorum Sensing, Virulence, Protein Secretion, Antibiotic Regulation and Bacteriophage Abortive Infection

Research Groupings: Structural and molecular cell biology | Infection and Immunity

 
image of culture plate and quorum sensing molecules
 
Quorum sensing controls production of a carbapenem antibiotic and prodigiosin in Serratia
   
 
Biosynthetic and regulatory prodigiosin mutants of  Serratia
 
Biosynthetic and regulatory prodigiosin mutants of Serratia

Our research involves multiple aspects of molecular microbiology including quorum sensing (QS), molecular pathogenesis in plant and animal pathogens, regulation and biosynthesis of antibiotics and other secondary metabolites, protein secretion systems, bacteriophage exploitation and viral abortive infection systems. We work on various Gram-negative enterobacteria, including the phytopathogen, Erwinia (Pectobacterium), Serratia species, which can be opportunistic human pathogens, Citrobacter rodentium the murine pathogen, and a spectrum of phages infecting various bacteria of fundamental, medical, agricultural or industrial biotechnology interest.

We are investigating the phenomenon of quorum sensing in which bacteria make small diffusible molecules (N-acyl homoserine lactones) as chemical communication signals reflecting cell population density status. The phenotypes regulated by quorum sensing include virulence, and exoenzyme and antibiotic production. Our research aims are to understand molecular mechanisms involved in quorum sensing, and dissect their physiological role(s), evolution and potential use in synthetic biology. We  study the genetics and biochemistry of carbapenem and prodiginine antibiotic synthesis in Erwinia and Serratia. We use genetics, transcriptomics and proteomics to investigate the physiological impacts of environmental signaling in regulation to virulence and antibiotic production in Erwinia, Serratia and Citrobacter. We also investigate molecular processes involved in proteinaceous virulence factor secretion in Erwinia. We are investigating new bacteriophages that attack a range of enteric bacteria, both in terms of host range and for the development of new genetic tools for functional genomics. We are also studying phage abortive infection systems (with bifunctional toxin:antitoxin capacity) through which bacteria control the replication of their viral parasites. The latter project also involves collaborative structural biology work.

DIGE gel
Bacteriophages of the murine pathogen, Citobacter rodentium
DiGE proteomics of Erwinia (green, secreted; red, intracellular)
Bacteriophages of the murine pathogen, Citrobacter rodentium

Lab members
Katinka Apagyi, Tim Blower, Tim Carlton, Marion Cubitt, Rita Monson, Simon Poulter, Joshua Ramsay, Alison Rawlinson, Kevin Roberts, Francesca Short, Hui Tan, Evelyn Tichy, Nabil Wilf, Neil Williamson

References

  1. Fineran, P., Blower, TR., Foulds, IJ., Humphreys, D, Lilley, KS and Salmond, GPC (2009) The phage abortive infection system, ToxIN, functions as a protein-RNA toxin-antitoxin pair. PNAS, USA, 106: 894-899
  2. Williamson, N., Fineran, P., Leeper, F. and Salmond, GPC (2006) The biosynthesis and regulation of bacterial prodiginines. Nature Reviews Microbiology, 4, 887-899
  3. Coulthurst, S., Barnard, A. and Salmond, GPC (2005) Regulation and biosynthesis of carbapenem antibiotics in bacteria. Nature Reviews Microbiology 3:295-306
  4. Whitehead, N., Barnard, AML., Slater, H., Simpson, NJL and Salmond, GPC (2001) Quorum sensing in Gram-negative bacteria. FEMS Microbiological Reviews, 25, 365-404
  5. Welch, M., Todd, DE., Whitehead, NA., McGowan, SJ., Bycroft, BW. and Salmond, GPC. (2000) N-acyl homoserine lactone binding to the CarR receptor determines quorum-sensing specificity in Erwinia. EMBO J. 19, 631-641

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