Impaired Alanine Transport or Exposure to d-Cycloserine Increases the Susceptibility of MRSA to β-lactam Antibiotics. (19th October 2019)

• Record Type: Journal Article
• Authors: Gallagher, Laura A; Shears, Rebecca K; Fingleton, Claire; Alvarez, Laura; Waters, Elaine M; Clarke, Jenny; Bricio-Moreno, Laura; Campbell, Christopher; Yadav, Akhilesh K; Razvi, Fareha; O'Neill, Eoghan; O'Neill, Alex J; Cava, Felipe; Fey, Paul D; Kadioglu, Aras; O'Gara, James P
• Is Part Of: Journal of infectious diseases. Volume 221:Number 6(2020)
• Page Start: 1000
• Page End: 1016
• Publication Date: 2019-10-19
• Subjects: antibiotic resistance -- MRSA -- β-lactam resistance -- alanine transport -- d-cycloserine; Communicable diseases -- Periodicals; Diseases -- Causes and theories of causation -- Periodicals; Medicine -- Periodicals; Communicable Diseases -- Periodicals; Electronic journals; 616.9
• DOI: 10.1093/infdis/jiz542
• Languages: English
• ISSNs: 0022-1899

Abstract

Abstract: Prolonging the clinical effectiveness of β-lactams, which remain first-line antibiotics for many infections, is an important part of efforts to address antimicrobial resistance. We report here that inactivation of the predicted d -cycloserine (DCS) transporter gene cycA resensitized methicillin-resistant Staphylococcus aureus (MRSA) to β-lactam antibiotics. The cycA mutation also resulted in hypersusceptibility to DCS, an alanine analogue antibiotic that inhibits alanine racemase and d -alanine ligase required for d -alanine incorporation into cell wall peptidoglycan. Alanine transport was impaired in the cycA mutant, and this correlated with increased susceptibility to oxacillin and DCS. The cycA mutation or exposure to DCS were both associated with the accumulation of muropeptides with tripeptide stems lacking the terminal d -ala-d -ala and reduced peptidoglycan cross-linking, prompting us to investigate synergism between β-lactams and DCS. DCS resensitized MRSA to β-lactams in vitro and significantly enhanced MRSA eradication by oxacillin in a mouse bacteremia model. These findings reveal alanine transport as a new therapeutic target to enhance the susceptibility of MRSA to β-lactam antibiotics.