1. Molecular epidemiology of Neisseria meningitidis serogroup B in Brazil.
- Author
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de Filippis I, de Lemos AP, Hostetler JB, Wollenberg K, Sacchi CT, Dunning Hotopp JC, Harrison LH, Bash MC, and Prevots DR
- Subjects
- Bacterial Typing Techniques, Base Sequence, Biodiversity, Brazil epidemiology, Genes, Bacterial genetics, Genetic Variation, Geography, Humans, Likelihood Functions, Meningococcal Infections genetics, Molecular Epidemiology, Molecular Sequence Data, Multilocus Sequence Typing, Neisseria meningitidis, Serogroup B classification, Neisseria meningitidis, Serogroup B isolation & purification, Phylogeny, Time Factors, Meningococcal Infections epidemiology, Meningococcal Infections microbiology, Neisseria meningitidis, Serogroup B genetics
- Abstract
Background: Neisseria meningitidis serogroup B has been predominant in Brazil, but no broadly effective vaccine is available to prevent endemic meningococcal disease. To understand genetic diversity among serogroup B strains in Brazil, we selected a nationally representative sample of clinical disease isolates from 2004, and a temporally representative sample for the state of São Paulo (1988-2006) for study (nā=ā372)., Methods: We performed multi-locus sequence typing (MLST) and sequence analysis of five outer membrane protein (OMP) genes, including novel vaccine targets fHbp and nadA., Results: In 2004, strain B:4:P1.15,19 clonal complex ST-32/ET-5 (cc32) predominated throughout Brazil; regional variation in MLST sequence type (ST), fetA, and porB was significant but diversity was limited for nadA and fHbp. Between 1988 and 1996, the São Paulo isolates shifted from clonal complex ST-41/44/Lineage 3 (cc41/44) to cc32. OMP variation was associated with but not predicted by cc or ST. Overall, fHbp variant 1/subfamily B was present in 80% of isolates and showed little diversity. The majority of nadA were similar to reference allele 1., Conclusions: A predominant serogroup B lineage has circulated in Brazil for over a decade with significant regional and temporal diversity in ST, fetA, and porB, but not in nadA and fHbp.
- Published
- 2012
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