J. Bogaerts et al., ANTIMICROBIAL RESISTANCE AND SEROTYPES OF SHIGELLA ISOLATES IN KIGALI, RWANDA (1983 TO 1993) - INCREASING FREQUENCY OF MULTIPLE RESISTANCE, Diagnostic microbiology and infectious disease, 28(4), 1997, pp. 165-171
The serotype distribution and susceptibility to nine antibiotics was d
etermined for 2491 Shigella isolates cultured in the medical laborator
y of the Centre Hospitalier de Kigali, Rwanda, during 1983 to 1993. Ov
erall, Shigella flexneri was the most frequent species, ranking before
Shigella sonnei, Shigella boydii, and Shigella dysenteriae. However,
the relative frequency of the different Shigella spp. showed an import
ant variability over time. S. flexneri increased from 40% in 1983 to 6
8% of the isolates in 1993 whereas S. dysenteriae Type I decreased gra
dually from 30 to 0.5% of the isolates in 1992. After the outbreak of
severe civil unrest, which caused the displacement of many people to t
he capital, a new epidemic of dysentery started in the Kigali area and
S. dysenteriae Type I accounted again for 24% of the isolates in 1993
. In 1983, resistance to tetracycline, streptomycin, and sulfonamides
was common among the endemic Shigella spp. Resistance to chloramphenic
ol was observed in 17% (30/182) of the isolates. Only 10% were resista
nt to ampicillin and an equal proportion to trimethoprim, whereas 5% o
f the isolates showed resistance to both products. By 1993, 66% (195/2
95) of the isolates were resistant to chloramphenicol (for comparison
with 1983, p < 0.001), 70% (207/295) to ampicillin (p < 0.001), 67% to
trimethoprim (p < 0.001), and 58% had combined resistance to the latt
er two drugs (p < 0.001). Resistance patterns differed strongly by spe
cies, S. flexneri being more frequently resistant than S. sonnei. In 1
983, all S. dysenteriae Type 1 isolates were resistant to ampicillin,
chloramphenicol, tetracycline, and sulfonamides. Trimethoprim resistan
ce increased from 31% (25/80) in 1983 to 96% (26/27) of the isolates i
n 1986 (p < 0.002). After the introduction of nalidixic acid as an alt
ernative for trimethoprim-sulfamethoxazole, trimethoprim resistance de
creased to 87%, during 1987 to 1992, and subsequently to 68% of the is
olates in 1993. However, 20% of the isolates became resistant to nalid
ixic acid in 1993. Ampicillin and trimethoprim-sulfamethoxazole ave no
longer useful for the empirical treatment of shigellosis in Rwanda. (
C) 1997 Elsevier Science Inc.