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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.
Abstract:
Quinolone resistance is increasing in Neisseria meningitidis, with its prevalence in China being high (>70%), but its origin remains unknown. The aim of this study was to investigate the donors of mutation-harboring gyrA alleles in N. meningitidis A total of 198 N. meningitidis isolates and 293 commensal Neisseria isolates were collected between 2005 and 2018 in Shanghai, China. The MICs of ciprofloxacin were determined using the agar dilution method. The resistance-associated genes gyrA and parC were sequenced for all isolates, while a few isolates were sequenced on the Illumina platform. The prevalences of quinolone resistance in the N. meningitidis and commensal Neisseria isolates were 67.7% (134/198) and 99.3% (291/293), respectively. All 134 quinolone-resistant N. meningitidis isolates possessed mutations in T91 (n = 123) and/or D95 (n = 12) of GyrA, with 7 isolates also harboring ParC mutations and exhibiting higher MICs. Phylogenetic analysis of the gyrA sequence identified six clusters. Among the 71 mutation-harboring gyrA alleles found in 221 N. meningitidis isolates and genomes (n = 221), 12 alleles (n = 103, 46.6%) were included in the N. meningitidis cluster, while 20 alleles (n = 56) were included in the N. lactamica cluster, 27 alleles (n = 49) were included in the N. cinerea cluster, and 9 alleles (n = 10) were included in the N. subflava cluster. Genomic analyses identified the exact N. lactamica donors of seven mutation-harboring gyrA alleles (gyrA92, gyrA97, gyrA98, gyrA114, gyrA116, gyrA151, and gyrA230) and the N. subflava donor isolate of gyrA171, with the sizes of the recombinant fragments ranging from 634 to 7,499 bp. Transformation of gyrA fragments from these donor strains into a meningococcal isolate increased its ciprofloxacin MIC from 0.004 μg/ml to 0.125 or 0.19 μg/ml and to 0.5 μg/ml with further transformation of an additional ParC mutation. Over half of the quinolone-resistant N. meningitidis isolates acquired resistance by horizontal gene transfer from three commensal Neisseria species. Quinolone resistance in N. meningitidis increases in a stepwise manner.
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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