Related Experiment Video
Updated: May 18, 2026

Inducing Meningococcal Meningitis Serogroup C in Mice via Intracisternal Delivery
Published on: November 5, 2019
Persistence of hyperinvasive meningococcal strain types during global spread as recorded in the PubMLST database
Eleanor R Watkins1, Martin C J Maiden
1Department of Zoology, University of Oxford, Oxford, United Kingdom.
Abstract:
Neisseria meningitidis is a major cause of septicaemia and meningitis worldwide. Most disease in Europe, the Americas and Australasia is caused by meningococci expressing serogroup B capsules, but no vaccine against this polysaccharide exists. Potential candidates for 'serogroup B substitute' vaccines are outer membrane protein antigens including the typing antigens PorA and FetA. The web-accessible PubMLST database (www.pubmlst.org) was used to investigate the temporal and geographical patterns of associations among PorA and FetA protein variants and lineages defined by combinations of housekeeping genes, known as clonal complexes. The sample contained 3460 isolates with genotypic information from 57 countries over a 74 year period. Although shifting associations among antigen variants and clonal complexes were evident, a subset of strain types associated with several serogroups persisted for decades and proliferated globally. Genetic stability among outer membrane proteins of serogroup A meningococci has been described previously, but here long-lived genetic associations were also observed among meningococci belonging to serogroups B and C. The patterns of variation were consistent with behaviour predicted by models that invoke inter-strain competition mediated by immune selection. There was also substantial geographic and temporal heterogeneity in antigenic repertoires, providing both opportunities and challenges for the design of broad coverage protein-based meningococcal vaccines.
Insights
Neisseria meningitidis serogroup B strains show persistent genetic associations, posing challenges for vaccine development. Understanding these patterns is crucial for creating effective meningococcal vaccines.
Area of Science:
- Microbiology
- Immunology
- Epidemiology
Background:
- Neisseria meningitidis causes global septicaemia and meningitis.
- Serogroup B strains are prevalent in Europe, Americas, and Australasia, yet lack a polysaccharide vaccine.
- Outer membrane proteins like PorA and FetA are potential vaccine candidates.
Purpose of the Study:
- To investigate temporal and geographical patterns of associations between Neisseria meningitidis outer membrane protein variants (PorA, FetA) and clonal complexes.
- To identify persistent strain types and understand their global proliferation.
- To assess the implications for designing broad-coverage protein-based meningococcal vaccines.
Main Methods:
- Utilized the PubMLST database containing genotypic information from 3460 isolates.
- Analyzed data from 57 countries spanning a 74-year period.
- Examined associations among PorA and FetA protein variants and housekeeping gene-defined lineages (clonal complexes).
Main Results:
- Identified shifting associations between antigen variants and clonal complexes.
- Observed a subset of persistent strain types associated with multiple serogroups, proliferating globally over decades.
- Found long-lived genetic associations among serogroup B and C meningococci, similar to previously described stability in serogroup A.
- Noted geographic and temporal heterogeneity in antigenic repertoires.
Conclusions:
- Long-lived genetic associations among Neisseria meningitidis outer membrane proteins, particularly in serogroups B and C, persist globally.
- These patterns suggest immune selection and inter-strain competition drive variation.
- The antigenic heterogeneity presents both opportunities and challenges for developing effective, broad-coverage protein-based meningococcal vaccines.
Related Concept Videos
Bacterial Meningitis I: Introduction
Bacterial Meningitis II: Pathophysiology
Clinical Significance of Antibiotic Resistance
Mechanism of Antibiotic Resistance in MRSA
Viral Meningitis
Colonisation of Pathogens
