Molecular Characterization of Invasive Meningococcal Isolates from Countries in the African Meningitis Belt before Introduction of a Serogroup A Conjugate Vaccine

被引:43
作者
Caugant, Dominique A. [1 ,2 ]
Kristiansen, Paul A. [1 ]
Wang, Xin [3 ]
Mayer, Leonard W. [3 ]
Taha, Muhamed-Kheir [4 ]
Ouedraogo, Rasmata [5 ]
Kandolo, Denis [6 ]
Bougoudogo, Flabou [7 ]
Sow, Samba [8 ]
Bonte, Laurence [9 ]
机构
[1] Norwegian Inst Publ Hlth, WHO Collaborating Ctr Reference & Res Meningococc, Oslo, Norway
[2] Univ Oslo, Fac Med, Oslo, Norway
[3] Ctr Dis Control & Prevent, WHO Collaborating Ctr Prevent & Control Epidem Me, Atlanta, GA USA
[4] Inst Pasteur, WHO Collaborating Ctr Reference & Res Meningococc, Paris, France
[5] Ctr Hosp Univ Pediat Charles de Gaulle, Lab Reference Meningite, Ouagadougou, Burkina Faso
[6] WHO Inter Country Support Team W Africa, Ouagadougou, Burkina Faso
[7] INRSP, Bamako, Mali
[8] CVD, Bamako, Mali
[9] Med Sans Frontieres, Support Logist, Paris, France
关键词
NEISSERIA-MENINGITIDIS; BURKINA-FASO; W135; DISEASE; EPIDEMIC; EMERGENCE; OUTBREAK; STRAIN; NIGER;
D O I
10.1371/journal.pone.0046019
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
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.
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