AI Article Synopsis

  • Neisseria gonorrhoeae poses a significant public health risk due to rising cases and antimicrobial resistance, with whole-genome sequencing (WGS) evaluated for predicting susceptibility to various antimicrobials.
  • 481 isolates from five countries were analyzed, revealing that susceptibility to ciprofloxacin is linked to a specific genetic marker (gyrA codon 91), while predicting susceptibility to other drugs requires a multilocus approach.
  • All isolates tested were susceptible to zolifodacin, and while a single marker can guide ciprofloxacin treatment, a combination of markers is necessary for other medications.

Article Abstract

Background: Neisseria gonorrhoeae is a major public health problem due to increasing incidence and antimicrobial resistance. Genetic markers of reduced susceptibility have been identified; the extent to which those are representative of global antimicrobial resistance is unknown. We evaluated the performance of whole-genome sequencing (WGS) used to predict susceptibility to ciprofloxacin and other antimicrobials using a global collection of N. gonorrhoeae isolates.

Methods: Susceptibility testing of common antimicrobials and the recently developed zolifodacin was performed using agar dilution to determine minimum inhibitory concentrations (MICs). We identified resistance alleles at loci known to contribute to antimicrobial resistance in N. gonorrhoeae from WGS data. We tested the ability of each locus to predict antimicrobial susceptibility.

Results: A total of 481 N. gonorrhoeae isolates, collected between 2004 and 2019 and making up 457 unique genomes, were sourced from 5 countries. All isolates with demonstrated susceptibility to ciprofloxacin (MIC ≤0.06 μg/mL) had a wild-type gyrA codon 91. Multilocus approaches were needed to predict susceptibility to other antimicrobials. All isolates were susceptible to zoliflodacin, defined by an MIC ≤0.25 μg/mL.

Conclusions: Single marker prediction can be used to inform ciprofloxacin treatment of N. gonorrhoeae infection. A combination of molecular markers may be needed to determine susceptibility for other antimicrobials.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10319951PMC
http://dx.doi.org/10.1093/infdis/jiad027DOI Listing

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