AI Article Synopsis

  • Invasive meningococcal isolates in South Africa have shown a consistent presence of serogroups B, C, W, and Y between 2016-2021, with an intermediate penicillin resistance rate of 16%.
  • A total of 585 invasive meningococcal disease cases were monitored, with phenotypic and genomic analyses revealing key serogroups and clonal complexes.
  • The increased penicillin intermediate resistance was linked to specific penA gene mosaics, indicating a concerning rise in antibiotic resistance among these bacteria compared to prior years.

Article Abstract

Background: Invasive meningococcal isolates in South Africa have in previous years (<2008) been characterized by serogroup B, C, W, and Y lineages over time, with penicillin intermediate resistance (peni) at 6%. We describe the population structure and genomic markers of peni among invasive meningococcal isolates in South Africa, 2016-2021.

Methods: Meningococcal isolates were collected through national, laboratory-based invasive meningococcal disease (IMD) surveillance. Phenotypic antimicrobial susceptibility testing and whole-genome sequencing were performed, and the mechanism of reduced penicillin susceptibility was assessed in silico.

Results: Of 585 IMD cases reported during the study period, culture and PCR-based capsular group was determined for 477/585 (82%); and 241/477 (51%) were sequenced. Predominant serogroups included NmB (210/477; 44%), NmW (116/477; 24%), NmY (96/477; 20%), and NmC (48/477; 10%). Predominant clonal complexes (CC) were CC41/44 in NmB (27/113; 24%), CC11 in NmW (46/56; 82%), CC167 in NmY (23/44; 53%), and CC865 in NmC (9/24; 38%). Peni was detected in 16% (42/262) of isolates, and was due to the presence of a penA mosaic, with the majority harboring penA7, penA9, or penA14.

Conclusions: IMD lineages circulating in South Africa were consistent with those circulating prior to 2008; however, peni was higher than previously reported, and occurred in a variety of lineages.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11646611PMC
http://dx.doi.org/10.1093/infdis/jiae225DOI Listing

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