Continuing genomic evolution of the Neisseria meningitidis cc11.2 urethritis clade, NmUC: a narrative review

• Authors: Emilio I. Rodriguez, Emory University; Yih-Ling Tzeng, Emory University; David Stephens, Emory University
• Journal Title: Microbial Genomics
• Volume: Volume 9, Number 10
• Publisher: Microbiology Society | 2023-10-01
• Type of Work: Article | Final Publisher PDF
• Publisher DOI: http://doi.org/10.1099/mgen.0.001113
• Subjects: Biology, Microbiology; Biology, Genetics
• Keywords: Neisseria gonorrhoeae; Neisseria meningitidis; NmUC; antimicrobial resistance; genomic evolution; urogenital pathogen; Humans; Neisseria meningitidis; Urethritis; Meningococcal Infections; Gonorrhea; Genomics; Evolution, Molecular

Abstract

Neisseria meningitidis (Nm) is a bacterial pathogen responsible for invasive meningococcal disease. Though typically coloniz-ing the nasopharynx, multiple outbreaks of meningococcal urethritis were first reported in 2015–2016; outbreaks originally presumed to be caused by Neisseria gonorrhoeae (Ng). Genomic analysis revealed that the Nm isolates causing these outbreaks were a distinct clade, and had integrated gonococcal DNA at multiple genomic sites, including the gonococcal denitrification apparatus aniA–norB, a partial gonococcal operon of five genes containing ispD, and the acetylglutamate kinase gene argB with the adjacent gonococcal locus NGO0843. The urethritis isolates had also deleted the group C capsule biosynthesis genes cssA/ B/C and csc, resulting in loss of capsule. Collectively, these isolates form the N. meningitidis urethritis clade (NmUC). Genomic analysis of recent (2016–2022) NmUC isolates revealed that the genomic features have been maintained in the clade, implying that they are important for NmUC’s status as a urogenital pathogen. Furthermore, the analysis revealed the emergence of a sub-clade, designated NmUC-B, phylogenetically separated from the earlier NmUC-A. This sub-clade has integrated additional gonococcal alleles into the genome, including alleles associated with antimicrobial resistance. NmUC continues to adapt to a urethral niche and evolve as a urogenital pathogen.