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Detection of a geographical and endemic cluster of hyper-invasive meningococcal strains
Sophie Bertrand1, Eva Van Meervenne, Thierry De Baere
1National Reference Centre for Neisseria meningitidis, Bacterial Diseases Division, Communicable and Infectious Diseases, Scientific Institute of Public Health, J. Wytsman Street, 14-16, B-1050 Brussels, Belgium. sophie.bertrand@wiv-isp.be
Abstract:
From 2006 to December 2009, 45 out of the 513 strains isolated from patients with invasive meningococcal disease in Belgium, were identified as Neisseria meningitidis serogroup B, non-serotypeable, subtype P1.14 (B:NT:P1.14). Most cases were geographically clustered in the northern part of the country. Multilocus Sequence Typing and antigen gene sequencing combined with Pulsed-Field Gel electrophoresis were used to investigate this cluster. Molecular typing showed that 39 out of these 45 N. meningitidis strains belonged to the clonal complex cc-269. The presence of the same PorA Variable Regions (VR1-VR2: 22, 14), the FetA allele (F5-1) and the highly similar Pulsed-Field Gel Electrophoresis profiles, supported genetic relatedness for 38 out of these 39 isolates. Retrospective analysis of B:NT:P1.22,14 isolates from 1999 onwards suggested that these strains belonging to the cc-269 complex, first emerged in the Belgian province of West-Flanders in 2004. This study showed that the combination of molecular tools with classical methods enabled reliable outbreak detection as well as a cluster identification.
Insights
A specific Neisseria meningitidis serogroup B strain (B:NT:P1.14) caused an invasive meningococcal disease outbreak in Belgium. Molecular analysis identified a dominant clonal complex (cc-269) responsible for the cluster, aiding in outbreak detection.
Area of Science:
- Microbiology
- Epidemiology
- Molecular Biology
Background:
- Invasive meningococcal disease (IMD) poses a significant public health threat.
- Serogroup B Neisseria meningitidis is a common cause of IMD outbreaks globally.
- Understanding strain characteristics and transmission dynamics is crucial for control.
Purpose of the Study:
- To investigate a cluster of invasive meningococcal disease cases in Belgium.
- To characterize the molecular features of the causative Neisseria meningitidis strains.
- To identify the origin and genetic relatedness of the implicated bacterial isolates.
Main Methods:
- Isolation and identification of Neisseria meningitidis strains from IMD patients.
- Molecular typing techniques including Multilocus Sequence Typing (MLST) and antigen gene sequencing.
- Pulsed-Field Gel Electrophoresis (PFGE) for assessing genetic relatedness.
- Retrospective analysis of historical isolates.
Main Results:
- 45 out of 513 IMD strains were identified as Neisseria meningitidis serogroup B, non-serotypeable, subtype P1.14 (B:NT:P1.14).
- A significant geographic cluster was observed in northern Belgium.
- Molecular typing revealed that 39 strains belonged to the clonal complex cc-269.
- Shared PorA VR1-VR2 (22, 14) and FetA (F5-1) alleles, along with similar PFGE profiles, confirmed genetic relatedness among 38 isolates.
- Retrospective analysis indicated the emergence of cc-269 strains in West-Flanders in 2004.
Conclusions:
- A specific B:NT:P1.14 Neisseria meningitidis strain belonging to cc-269 was responsible for an IMD outbreak in Belgium.
- The combination of molecular typing and classical methods proved effective for outbreak detection and cluster identification.
- Early emergence of this strain complex was identified, highlighting the importance of ongoing surveillance.
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