Mutations in sigma E regulated lipoproteins have previously been shown to impact on bacterial viability under conditions of stress and during in vivo infection. YraP is conserved across a number of Gram-negative pathogens, including Neisseria meningitidis where the homolog is a component of the Bexsero Meningococcal Group B vaccine. Investigations using laboratory adapted Escherichia coli K12 have shown that yraP mutants have elevated sensitivity to a range of compounds including detergents and normally ineffective antibiotics. In this study, we investigate the role of the outer membrane lipoprotein, YraP in the pathogenesis of Salmonella enterica serovar Typhimurium. We show that mutations in S. Typhimurium yraP result in a defective outer membrane barrier with elevated sensitivity to a range of compounds. This defect is associated with attenuated virulence in an oral infection model and during the early stages of systemic infection. We show this attenuation is not a result of defects in lipopolysaccharide and O-antigen synthesis, changes in outer membrane protein levels or the ability to adhere to and invade eukaryotic cell lines in vitro.
|Journal||Infection and Immunity|
|Early online date||10 Sept 2018|
|Publication status||Published - 25 Oct 2018|