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Re-emergence of Meningococcal Carriage on Three-year Follow-up of a Kibbutz Population After Whole-community Chemoprophylaxis

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Publisher Springer
Date 1993 Jul 1
PMID 8404910
Citations 3
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Abstract

A long-term study was conducted to determine the rate of re-emergence of throat carriage of meningococci in a semi-closed kibbutz community after the administration of chemoprophylaxis to all its members. Serotype B:4 was selected as marker organism since it was isolated from a fatal case and was the most frequently occurring strain (80%) among serogroup B isolates, which themselves comprised 54% of all meningococci. The carriage rate among Israeli residents (volunteer workers were analyzed separately) before treatment was 6.6% (49/748) overall, with 4.3% group B strains. Three weeks after treatment, in most cases with rifampicin (whereby three persistently positive persons were retreated with minocycline), no meningococci were recovered. Six months later, 1.9% of a population sample aged < or = 30 years were positive, while before treatment and one and three years later, 9.4%, 8.6% and 4.6% respectively were positive in this age group. Serotype B:4 comprised 81.3% of group B strains before prophylaxis, 5.3% after one year, and 28.6% after three years, thus possibly re-establishing itself as the single dominant serotype. The marked suppression of carriage after mass chemoprophylaxis appeared to last at least six months, with the meningococcal population being re-established within a year.

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References
1.
Dagan R, Ferne M, Sheinis M, Alkan M, KATZENELSON E . An epidemic of penicillin-tolerant group A streptococcal pharyngitis in children living in a closed community: mass treatment with erythromycin. J Infect Dis. 1987; 156(3):514-6. DOI: 10.1093/infdis/156.3.514. View

2.
Mocca L, Frasch C . Sodium dodecyl sulfate-polyacrylamide gel typing system for characterization of Neisseria meningitidis isolates. J Clin Microbiol. 1982; 16(2):240-4. PMC: 272337. DOI: 10.1128/jcm.16.2.240-244.1982. View

3.
Friedman M, Galil A, Sarov B, Margalith M, Katzir G, Midthun K . Two sequential outbreaks of rotavirus gastroenteritis: evidence for symptomatic and asymptomatic reinfections. J Infect Dis. 1988; 158(4):814-22. DOI: 10.1093/infdis/158.4.814. View

4.
Herman J, Keynan A . Long-interval transmission of meningococcal disease. J Infect Dis. 1980; 142(6):945. DOI: 10.1093/infdis/142.6.945. View

5.
Stuart J, Cartwright K, Jones D, Noah N, Wall R, Blackwell C . An outbreak of meningococcal disease in Stonehouse: planning and execution of a large-scale survey. Epidemiol Infect. 1987; 99(3):579-89. PMC: 2249254. DOI: 10.1017/s0950268800066437. View