Whole genome sequence analysis of Neisseria meningitidis strains circulating in Kazakhstan, 2017-2018

Alexandr Shevtsov1, Zabida Aushakhmetova2, Asylulan Amirgazin1

  • 1National Center for Biotechnology, Astana, Kazakhstan.

Plos One
|December 28, 2022
PubMed

Insights

This study reveals the genetic diversity of Neisseria meningitidis in Kazakhstan, identifying two novel sequence types (ST-16025 and ST-16027). ST-16025 was prevalent in both invasive disease cases and asymptomatic carriers, highlighting its importance.

Area of Science:

  • Microbiology
  • Genomics
  • Epidemiology

Background:

  • Neisseria meningitidis causes severe meningeal inflammation and sepsis.
  • Genetic and antigenic diversity necessitates strain genotyping for effective vaccine matching.
  • Meningococcal disease incidence in Kazakhstan ranges from 0.2 to 2.5 cases per 100,000 population annually.

Purpose of the Study:

  • To investigate the genetic diversity of Neisseria meningitidis strains in Kazakhstan.
  • To identify novel sequence types (STs) and characterize circulating strains.
  • To provide data supporting potential changes in diagnostic protocols.

Main Methods:

  • Isolation and sequencing of 41 N. meningitidis strains from clinical patients and contacts (2017-2018).
  • In silico typing using Neisseria pipeline 1.2 and PubMLST.
  • Whole genome SNP (single nucleotide polymorphism) tree construction using BioNumerics 8.
  • Seven-gene multilocus sequence typing (MLST) for strain identification.

Main Results:

  • Ten sequence types (STs) were identified, including two novel types: ST-16025 and ST-16027.
  • ST-16025 was detected in invasive disease patients and asymptomatic contacts, showing significant intertypic diversity (>2000 SNPs).
  • Invasive and carrier strains belonged to different serogroups (MenB, MenC, MenW) and varied in PorA, FetA, fHbp, and NHBA alleles.

Conclusions:

  • This is the first report on N. meningitidis genetic diversity in Kazakhstan.
  • The prevalent ST-16025 warrants further surveillance due to its presence in both invasive and carrier states.
  • The findings support enhanced sample collection for whole genome sequencing (WGS) in routine diagnostics.