Meningococcal Quinolone Resistance Originated from Several Commensal Neisseria Species

Mingliang Chen1,2, Chi Zhang3, Xi Zhang3

  • 1Department of Microbiology, Shanghai Municipal Center for Disease Control and Prevention, Shanghai, China chenmingliang@scdc.sh.cn chenmin@scdc.sh.cn.

Insights

Quinolone resistance in Neisseria meningitidis is increasing due to horizontal gene transfer from commensal Neisseria species. This study identified Neisseria lactamica and Neisseria subflava as key donors of resistance-conferring gyrA alleles.

Area of Science:

  • Microbiology
  • Genetics
  • Antimicrobial Resistance

Background:

  • Increasing quinolone resistance in Neisseria meningitidis, particularly in China, poses a significant public health concern.
  • The origin and transmission pathways of quinolone resistance-associated mutations in N. meningitidis remain largely unknown.

Purpose of the Study:

  • To investigate the sources of mutation-harboring gyrA alleles in Neisseria meningitidis isolates.
  • To elucidate the role of commensal Neisseria species in the emergence and spread of quinolone resistance in N. meningitidis.

Main Methods:

  • Collection and analysis of 198 N. meningitidis and 293 commensal Neisseria isolates from Shanghai, China (2005-2018).
  • Determination of ciprofloxacin Minimum Inhibitory Concentrations (MICs) using agar dilution.
  • Sequencing of gyrA and parC genes, with additional Illumina sequencing for genomic analysis.
  • Phylogenetic analysis of gyrA sequences and identification of gene donors through genomic analysis and transformation experiments.

Main Results:

  • High prevalence of quinolone resistance observed: 67.7% in N. meningitidis and 99.3% in commensal Neisseria.
  • All resistant N. meningitidis isolates harbored gyrA mutations (T91 and/or D95); 7 also had parC mutations.
  • Phylogenetic analysis revealed N. meningitidis gyrA alleles clustering with commensal species, notably N. lactamica and N. subflava.
  • Genomic analysis identified specific N. lactamica and N. subflava strains as donors of mutation-harboring gyrA alleles.
  • Transformation experiments confirmed that acquired gyrA fragments increase ciprofloxacin MICs in N. meningitidis.

Conclusions:

  • Horizontal gene transfer from commensal Neisseria species, particularly N. lactamica and N. subflava, is a major driver of quinolone resistance in N. meningitidis.
  • Quinolone resistance in N. meningitidis develops through stepwise acquisition of resistance-conferring mutations.
  • Understanding these transmission dynamics is crucial for combating antimicrobial resistance in pathogenic Neisseria.

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