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Journal of Clinical Microbiology, April 2007, p. 1266-1273, Vol. 45, No. 4
0095-1137/07/$08.00+0 doi:10.1128/JCM.02510-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Division of Medical Biology, Bacteriology Department, Adolfo Lutz Institute, São Paulo 01246-902, Brazil,1 Division of Medical Biology, Immunology Department, Adolfo Lutz Institute, São Paulo 01246-902, Brazil,2 Center for Epidemiological Surveillance Prof. Alexandre Vranjac, São Paulo 01246-902, Brazil3
Received 14 December 2006/ Returned for modification 5 February 2007/ Accepted 7 February 2007
Meningococcal disease is characterized by cyclic fluctuations in incidence, serogroup distribution, and antigenic profiles. In greater São Paulo, Brazil, there has been a constant increase in the incidence of serogroup C meningococcal disease since the late 1980s. To gain an understanding of changes in serogroup C meningococcal disease over three decades in greater São Paulo, Brazil, 1,059 invasive Neisseria meningitidis serogroup C isolates from 1976 and 2005 were analyzed. Three major clone complexes, sequence type (ST)-11, ST-8, and ST-103, were identified by multilocus sequence typing, and the isolates were characterized by serotyping and 16S rRNA typing. During the 30-year period, there were two major antigenic replacements: from 2a:P1.(5,2) to 2b:P1.3 and subsequently to 23:P1.14-6. All strains of clone ST-103 were characterized as serotype 23 and serosubtype P1.14-6. The origin of 23:P1.14-6 ST-103 complex strains is unknown, but efforts are needed to monitor its spread and define its virulence. The antigenic replacements we observed likely represent a mechanism to sustain meningococcal disease in the population as immunity to circulating strains accumulated.
Published ahead of print on 21 February 2007.
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