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Published on: November 5, 2019
Vaccine preventability of meningococcal clone, Greater Aachen Region, Germany
Johannes Elias1, Leo M Schouls, Ingrid van de Pol
1University of Wuerzburg, Wuerzburg, Germany. jelias@hygiene.uni-wuerzburg.de
Abstract:
Emergence of serogroup B meningococci of clonal complex sequence type (ST) 41/44 can cause high levels of disease, as exemplified by a recent epidemic in New Zealand. Multiplication of annual incidence rates (3.1 cases/100,000 population) of meningococcal disease in a defined German region, the city of Aachen and 3 neighboring countries (Greater Aachen) prompted us to investigate and determine the source and nature of this outbreak. Using molecular typing and geographic mapping, we analyzed 1,143 strains belonging to ST41/44 complex, isolated from persons with invasive meningococcal disease over 6 years (2001-2006) from 2 German federal states (total population 26 million) and the Netherlands. A spatially slowly moving clone with multiple-locus variable-number tandem repeat analysis type 19, ST42, and antigenic profile B:P1.7-2,4:F1-5 was responsible for the outbreak. Bactericidal activity in serum samples from the New Zealand MeNZB vaccination campaign confirmed vaccine preventability. Because this globally distributed epidemic strain spreads slowly, vaccination efforts could possibly eliminate meningococcal disease in this area.
Insights
Serogroup B meningococcal disease outbreaks, caused by a specific clone (ST 41/44), can be controlled. This slow-spreading strain, responsible for increased incidence in Germany and the Netherlands, is vaccine-preventable.
Area of Science:
- Microbiology
- Epidemiology
- Vaccinology
Background:
- Serogroup B meningococci, particularly clonal complex sequence type (ST) 41/44, are associated with significant disease burdens.
- A notable increase in meningococcal disease incidence was observed in the Greater Aachen region of Germany.
Purpose of the Study:
- To investigate the source and characteristics of the meningococcal disease outbreak in the Greater Aachen region.
- To analyze the molecular epidemiology and geographic spread of ST 41/44 strains.
Main Methods:
- Molecular typing techniques, including multiple-locus variable-number tandem repeat analysis (MLVA).
- Geographic mapping of invasive meningococcal disease (IMD) cases.
- Analysis of 1,143 Neisseria meningitidis strains isolated between 2001 and 2006.
Main Results:
- A specific clone, identified as MLVA type 19, ST 42, with antigenic profile B:P1.7-2,4:F1-5, was identified as the cause of the outbreak.
- This clone exhibited slow spatial dissemination across German federal states and the Netherlands.
- Serum samples from New Zealand's MeNZB vaccination campaign demonstrated bactericidal activity against the identified strain, confirming vaccine preventability.
Conclusions:
- The identified ST 41/44 clone is a significant driver of meningococcal disease in the studied region.
- The slow spread of this epidemic strain suggests that targeted vaccination strategies could potentially eliminate meningococcal disease in affected areas.
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