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Genotype‐Specific Carriage ofNeisseria meningitidisin Georgia Counties with Hyper‐ and Hyposporadic Rates of Meningococcal Disease
Author(s) -
Scott Kellerman,
Katherine McCombs,
Marsha Ray,
Wendy Baughman,
Michael Reeves,
Tanja Popović,
Nancy E. Rosenstein,
Monica M. Farley,
Paul A. Blake,
David S. Stephens
Publication year - 2002
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/341067
Subject(s) - carriage , neisseria meningitidis , meningococcal disease , incidence (geometry) , medicine , neisseriaceae , meningococcal vaccine , genotype , multilocus sequence typing , virology , microbiology and biotechnology , biology , antibiotics , genetics , bacteria , physics , pathology , optics , gene
Carriage of Neisseria meningitidis in a Georgia county with hypersporadic incidence of meningococcal disease ("hypersporadic county") and in a county with no cases of meningococcal disease was determined by a cross-sectional pharyngeal culture study of high school students. Among 2730 students from whom culture samples were obtained, meningococcal carriage was 7.7% (140/1818) in the hypersporadic county and 6.1% (56/912) in the comparison county. Carriage rates by serogroup and genetic type (i.e., electrophoretic type [ET]) did not differ significantly between counties, but apartment or mobile home residency was a risk factor for carriage in the hypersporadic county. Although most cases of meningococcal disease in the hypersporadic county were caused by members of the serogroup C ET-37 clonal group, no ET-37 meningococcal isolates were recovered from carriers in this county. However, 38% of all meningococcal isolates recovered from carriers in both counties were members of the serogroup Y ET-508 clonal group, an emerging cause of meningococcal disease in Georgia and throughout the United States during 1996-2001. Shifts in carriage and transmission of meningococcal strains with different pathogenic potential are important determinants of meningococcal disease incidence.

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