Development of a novel core genome MLST scheme for tracing multidrug resistant Staphylococcus capitis

Nat Commun. 2022 Jul 22;13(1):4254. doi: 10.1038/s41467-022-31908-x.

Abstract

Staphylococcus capitis, which causes bloodstream infections in neonatal intensive care units, is a common cause of healthcare-associated infections. Thus, a standardized high-resolution typing method to document the transmission and dissemination of multidrug-resistant S. capitis isolates is required. We aimed to establish a core genome multilocus sequence typing (cgMLST) scheme to surveil S. capitis. The cgMLST scheme was defined based on primary and validation genome sets and tested with outbreaks of linezolid-resistant isolates and a validation set. Phylogenetic analysis was performed to investigate the population structure and compare it with the result of cgMLST analysis. The S. capitis population consists of 1 dominant, NRCS-A, and 4 less common clones. In this work, a multidrug-resistant clone (L clone) with linezolid resistance is identified. With the features of type III SCCmec and multiple copies of mutations of G2576T and C2104T in the 23S rRNA, the L clone has been spreading silently across China.

MeSH terms

  • Anti-Bacterial Agents / pharmacology
  • Anti-Bacterial Agents / therapeutic use
  • Humans
  • Infant, Newborn
  • Linezolid / pharmacology
  • Linezolid / therapeutic use
  • Methicillin-Resistant Staphylococcus aureus* / genetics
  • Multilocus Sequence Typing / methods
  • Phylogeny
  • Staphylococcal Infections* / drug therapy
  • Staphylococcal Infections* / epidemiology
  • Staphylococcus capitis* / genetics

Substances

  • Anti-Bacterial Agents
  • Linezolid