Nature Communications (Oct 2023)

Cryptic susceptibility to penicillin/β-lactamase inhibitor combinations in emerging multidrug-resistant, hospital-adapted Staphylococcus epidermidis lineages

  • Xiaoliang Ba,
  • Claire L. Raisen,
  • Olivier Restif,
  • Lina Maria Cavaco,
  • Carina Vingsbo Lundberg,
  • Jean Y. H. Lee,
  • Benjamin P. Howden,
  • Mette D. Bartels,
  • Birgit Strommenger,
  • Ewan M. Harrison,
  • Anders Rhod Larsen,
  • Mark A. Holmes,
  • Jesper Larsen

DOI
https://doi.org/10.1038/s41467-023-42245-y
Journal volume & issue
Vol. 14, no. 1
pp. 1 – 12

Abstract

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Abstract Global spread of multidrug-resistant, hospital-adapted Staphylococcus epidermidis lineages underscores the need for new therapeutic strategies. Here we show that many S. epidermidis isolates belonging to these lineages display cryptic susceptibility to penicillin/β-lactamase inhibitor combinations under in vitro conditions, despite carrying the methicillin resistance gene mecA. Using a mouse thigh model of S. epidermidis infection, we demonstrate that single-dose treatment with amoxicillin/clavulanic acid significantly reduces methicillin-resistant S. epidermidis loads without leading to detectable resistance development. On the other hand, we also show that methicillin-resistant S. epidermidis is capable of developing increased resistance to amoxicillin/clavulanic acid during long-term in vitro exposure to these drugs. These findings suggest that penicillin/β-lactamase inhibitor combinations could be a promising therapeutic candidate for treatment of a high proportion of methicillin-resistant S. epidermidis infections, although the in vivo risk of resistance development needs to be further addressed before they can be incorporated into clinical trials.