Scientific Publication

Molecular characterization of invasive meningococcal isolates from countries in the African meningitis belt before introduction of a serogroup A conjugate vaccine

author(s) Sow, S.. - Bougoudogo, F.. - Bonte, L.. - Caugant, D.A.. - Kandolo, D.. - Mayer, L.W.. - Ouédraogo, R.. - Taha, M.K.. - Kristiansen, P.A..
from UK Foreign, Commonwealth & Development Office (FCDO)
permalink open
themes
regions
  • Northern America
  • Americas
  • World
  • Eastern Africa
  • Sub-Saharan Africa
  • Africa
  • Western Africa
  • Middle Africa
  • Northern Africa
citation

Caugant, D.A.; Kristiansen, P.A.; Wang X.; Mayer, L.W.; Taha, M.K.; Ouédraogo, R.; Kandolo, D.; Bougoudogo, F.; Sow, S.; Bonte, L. Molecular Characterization of Invasive Meningococcal Isolates from Countries in the African Meningitis Belt before Introduction of a Serogroup A Conjugate Vaccine. PLoS ONE (2012) 7 (9) e46019. (DOI: 10.1371/journal.pone.0046019)

Publications and datasets provided via GARDIAN

Abstract

Background The serogroup A conjugate meningococcal vaccine, MenAfriVac, was introduced in mass vaccination campaigns in December 2010 in Burkina Faso, Mali and Niger. In the coming years, vaccination will be extended to other African countries at risk of epidemics. To document the molecular characteristics of disease-causing meningococcal strains circulating in the meningitis belt of Africa before vaccine introduction, the World Health Organization Collaborating Centers on Meningococci in Europe and United States established a common strain collection of 773 isolates from cases of invasive meningococcal disease collected between 2004 and 2010 from 13 sub-Saharan countries. Methodology All isolates were characterized by multilocus sequence typing, and 487 (62%) were also analyzed for genetic variation in the surface antigens PorA and FetA. Antibiotic susceptibility was tested for part of the collection. Principal Findings Only 19 sequence types (STs) belonging to 6 clonal complexes were revealed. ST-5 clonal complex dominated with 578 (74.8%) isolates. All ST-5 complex isolates were remarkably homogeneous in their PorA (P1.20,9) and FetA (F3-1) and characterized the serogroup A strains which have been responsible for most epidemics during this time period. Sixty-eight (8.8%) of the 773 isolates belonged to the ST-11 clonal complex which was mainly represented by serogroup W135, while an additional 38 (4.9%) W135 isolates belonged to the ST-175 complex. Forty-eight (6.2%) serogroup X isolates from West Africa belonged to the ST-181 complex, while serogroup X cases in Kenya and Uganda were caused by an unrelated clone, ST-5403. Serogroup X, ST-181, emerged in Burkina Faso before vaccine introduction. Conclusions In the seven years preceding introduction of a new serogroup A conjugate vaccine, serogroup A of the ST-5 clonal complex was identified as the predominant disease-causing strain

Open original