Characteristics of Clonal Complex Changes and Quinolone Resistance-Determining Region Mutations of Levofloxacin-Resistant Streptococcus pneumoniae in South Korea

Microb Drug Resist. 2022 May;28(5):559-565. doi: 10.1089/mdr.2021.0341. Epub 2022 Mar 22.

Abstract

Streptococcus pneumoniae is the most common causative agent of community-acquired pneumonia and invasive pneumococcal diseases with high mortality rates. The aims of this study were to evaluate clonal complex (CC) changes of levofloxacin-resistant S. pneumoniae (LRSP) strains and to investigate the relationship between levofloxacin resistance and pneumococcal serotypes. We analyzed the antimicrobial susceptibility of 145 LRSP strains to 18 antimicrobial agents and the quinolone resistance-determining region mutation. Multilocus sequence typing was performed to investigate the genetic relatedness among LRSP strains. Most LRSP strains (96.6%) were multidrug resistant and had simultaneous mutations in gyrA, parC, and parE (91.7%). The serotypes 11A (44.1%) and 13 (14.5%) accounted for 58.6% of LRSP strains, and 32.0% were nonvaccine serotypes. Most LRSP strains were grouped as CC8279 (N = 83; 57.2%), CC189 (N = 10; 6.9%), or CC320 (N = 5; 3.4%). CC8279 was commonly combined with serotypes 11A and 13. There were numerous changes of serotype and CC accompanying the emergence and spread of LRSP. Continuous monitoring of changes in the serotype and sequence type of LRSP is required to follow the spread of LRSP for public health monitoring.

Keywords: Streptococcus pneumoniae; fluoroquinolones; levofloxacin; multilocus sequence typing; phenotype (serotyping).

MeSH terms

  • Anti-Bacterial Agents / pharmacology
  • Drug Resistance, Bacterial / genetics
  • Humans
  • Levofloxacin / pharmacology
  • Microbial Sensitivity Tests
  • Mutation
  • Pneumococcal Infections* / drug therapy
  • Pneumococcal Infections* / epidemiology
  • Quinolones* / pharmacology
  • Streptococcus pneumoniae / genetics

Substances

  • Anti-Bacterial Agents
  • Quinolones
  • Levofloxacin