Neisseria meningitidis (the meningococcus) is responsible for endemic
and epidemic meningococcal disease in Africa. Meningococci are placed
into 12 serogroups based on their capsular polysaccharide antigens. Gr
oup-B meningococci are responsible for sporadic endemic disease. In th
e meningitis belt of sub-Saharan Africa, the large spreading epidemics
which occur every 5-10 years are usually caused by group-A meningococ
ci, with attack rates of 400-500/100 000 population. In the last epide
mic, infection spread from the original meningitis belt to Kenya, Ugan
da, Rwanda, Zambia and Tanzania. Most cases of meningococcal disease a
re of meningitis and meningococcal septicaemia is a rare presentation
except in South Africa. It is important to exclude meningococcal septi
caemia since this carries the highest mortality (up to 75%). Treatment
involves intravenous chloramphenicol (or intramuscular, oily chloramp
henicol), a drug which is preferable to penicillin because penicillin-
resistant meningococci have already emerged in Africa. Dexamethasone t
reatment of meningococcal meningitis is unproven and may even be delet
erious in developing countries. Prevention of epidemic meningococcal d
isease could be achieved by mass vaccination with protein-conjugate, g
roup-A and -C polysaccharides, but these new vaccines are likely to be
expensive.