Bacteroides spp., particularly B. fragilis, are well-recognised bacter
ial pathogens. Production of the typical beta-lactamases of Bacteroide
s restricts the therapeutic use of beta-lactam agents mainly to the be
ta-lactamase inhibitor combinations and carbapenems. These compounds h
ave the advantage of broad-spectrum activity and the ability to combat
polymicrobial infections. Resistance of Bacteroides spp. to beta-lact
am antibiotics appears to be increasing, largely because of an overall
increase in beta-lactamase activity. There has been a rise in the pre
valence of isolates showing high-level production of typical Bacteroid
es beta-lactamases and an increase in reports other potent beta-lactam
ase types. In the case of B. fragilis, metallo-enzymes are a particula
r threat to current therapeutic practice, as they are not inhibited by
common beta-lactamase inhibitors and are able to hydrolyse carbapenem
s. The presence of permeability barriers may confer low-level beta-lac
tam resistance and supplement the effect of activity. There beta-lacta
mase are also sporadic reports of loss of beta-lactam activity because
of reduced affinity of the penicillin-binding proteins.