Identification of two genetic groups in Bacteroides fragilis by multilocusenzyme electrophoresis: distribution of antibiotic resistance (cfiA, cepA)and enterotoxin (bft) encoding genes
M. Gutacker et al., Identification of two genetic groups in Bacteroides fragilis by multilocusenzyme electrophoresis: distribution of antibiotic resistance (cfiA, cepA)and enterotoxin (bft) encoding genes, MICROBIO-UK, 146, 2000, pp. 1241-1254
Ninety-three Bacteroides fragilis strains of different origin were analysed
by multilocus enzyme electrophoresis (MLEE). Fourteen of the 15 genetic lo
ci analysed were polymorphic, whilst nucleoside phosphorylase was monomorph
ic. There was a mean of six alleles per locus and a mean genetic diversity
of 0.393. Cluster analysis identified 90 electrophoretic types (ETs) separa
ted into two major phylogenetic divisions at a genetic distance of 0.70. Di
vision I consisted of 81 ETs carrying the endogenous class A beta-lactamase
gene cepA, whereas division II comprised 9 ETs carrying the class B beta-l
actamase gene cfiA, but not cepA. The presence of these two genes was asses
sed by PCR and the expression of the cfiA gene was investigated by determin
ing the level of resistance to the antibiotic imipenem. MLEE showed a small
er genetic distance among the genotypes of the imipenem-resistant than amon
g the imipenem-susceptible strains. No other particular cluster was observe
d. The enterotoxin gene (bft) was detected by PCR: DNA sequencing of the pr
oducts obtained showed that the different bft alleles (bft-1. bft-2 and bft
-3) were scattered randomly troughout the phylogenetic tree. No association
between distinct clones and clinical manifestations (sepsis, abscesses, di
arrhoea), geographical origin or host origin (human or animal) could be fou
nd.