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Published on: September 11, 2020
Molecular characterisation of group A Neisseria meningitidis isolated in Sudan 1985-2001
Susanne Jacobsson1, Mohamed Issa, Magnus Unemo
1National Reference Laboratory for Pathogenic Neisseria, Department of Clinical Microbiology, Orebro University Hospital, Orebro, Sweden. susanne.jacobsson@orebroll.se
Abstract:
A total of 33 group A Neisseria meningitidis (Mc) isolates, collected in Sudan between 1985 and 2001, were studied in order to describe the changes over time in a country within the meningitis belt of Africa. The isolates were characterised by traditional phenotypic methods (serogrouping, serotyping, serosubtyping and antibiogram) and molecular techniques (genosubtyping, pulsed-field gel electrophoresis [PFGE] with restriction endonucleases SpeI and NheI, and multilocus sequence typing [MLST]). Three clones of group A Mc were identified: one before 1988 (sulphadiazine sensitive, serotype 4, genosubtype P1.7,13-1,35-1, sequence type 4 [ST-4]); another during and after the 1988 epidemic (sulphadiazine resistant, serotype 4, genosubtype P1.20,9,35-1, ST-5); and a third causing the 1999 epidemic (sulphadiazine resistant, serotype 4, genosubtype P1.20,9,35-1, ST-7). The first clone showed major differences compared to the other two. The second and third clones had many similarities with differences in only a single gene (pgm) in the MLST (47 of the 450 bp) but significant other differences according to the PFGE patterns. Within the clones, genosubtyping and MLST gave identical information (except one base substitution in the aroE gene in one isolate). However, the PFGE patterns showed changes over time within the clones, where SpeI revealed somewhat more diversity than NheI.
Insights
Three distinct clones of group A Neisseria meningitidis were identified in Sudan between 1985 and 2001. These clones showed genetic and phenotypic changes over time, impacting meningitis epidemiology in Africa.
Area of Science:
- Microbiology
- Epidemiology
- Genetics
Background:
- Neisseria meningitidis (Mc) is a major cause of bacterial meningitis, particularly in Africa's meningitis belt.
- Understanding the genetic evolution of circulating strains is crucial for disease control.
Purpose of the Study:
- To characterize changes in group A Neisseria meningitidis clones over time in Sudan.
- To describe the genetic and phenotypic diversity of Mc isolates from 1985 to 2001.
Main Methods:
- Phenotypic characterization: serogrouping, serotyping, serosubtyping, and antibiogram.
- Molecular techniques: genosubtyping, pulsed-field gel electrophoresis (PFGE) with SpeI and NheI, and multilocus sequence typing (MLST).
Main Results:
- Three distinct group A Mc clones were identified, associated with different time periods and epidemic events.
- Clone 1 (pre-1988) was sulphadiazine sensitive, while clones 2 (1988 epidemic) and 3 (1999 epidemic) were resistant.
- Clones 2 and 3 showed high similarity in MLST but distinct PFGE patterns, indicating genetic divergence over time.
Conclusions:
- The study identified significant clonal evolution of group A Neisseria meningitidis in Sudan.
- Changes in antibiotic resistance and genetic profiles of Mc clones influenced meningitis epidemiology.
- PFGE and MLST are valuable tools for tracking meningococcal evolution and outbreaks.
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