Molecular Epidemiology of Neisseria meningitidis Serogroup B in Brazil

被引:28
作者
de Filippis, Ivano [1 ,2 ,3 ]
de Lemos, Ana Paula S. [4 ]
Hostetler, Jessica B. [5 ]
Wollenberg, Kurt [6 ]
Sacchi, Claudio T. [7 ]
Harrison, Lee H. [8 ]
Bash, Margaret C. [2 ]
Prevots, D. Rebecca [3 ]
机构
[1] Oswaldo Cruz Fdn FIOCRUZ, Natl Qual Control Inst INCQS, Rio De Janeiro, Brazil
[2] US FDA, Lab Bacterial Polysaccharides, CBER, Bethesda, MD 20014 USA
[3] NIAID, Epidemiol Unit, Lab Clin Infect Dis, Div Intramural Res,NIH, Bethesda, MD 20892 USA
[4] IAL, Dept Bacteriol, Sao Paulo, Brazil
[5] JCVI, Rockville, MD USA
[6] NIAID, Off Cyberinfrastruct & Computat Biol OCICB, NIH, Bethesda, MD 20892 USA
[7] Adolfo Lutz Inst, Dept Immunol, Sao Paulo, Brazil
[8] Univ Pittsburgh, Infect Dis Epidemiol Res Unit, Pittsburgh, PA USA
基金
巴西圣保罗研究基金会; 美国国家卫生研究院;
关键词
FACTOR-H; MENINGOCOCCAL DISEASE; VACCINE CANDIDATE; SAO-PAULO; PROTEIN; DIVERSITY; STRAINS; NADA; PORA; IDENTIFICATION;
D O I
10.1371/journal.pone.0033016
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
07 ; 0710 ; 09 ;
摘要
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 Sao Paulo (1988-2006) for study (n = 372). 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 Sao 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.
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页数:10
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