Agar dilution MIC testing of amoxicillin, amoxicillin-BRL 42715, amoxicillin-clavulanate, temafloxacin, and clindamycin against 496 ,-lactamase-producing anaerobic gram-negative rods revealed MICs for 90o% of the strains tested of 256.0 (amoxicillin), 2.0 (amoxicillin-BRL 42715 and amoxicillin-clavulanate), and 4.0 (temafloxacin and clindamycin) ,ug/ml. Amoxicillin, temafloxacin, and clindamycin inhibited all 44 13-lactamase-negative strains (MICs for 90%o of the strains tested, <2.0 ,ug/ml). BRL 42715 will not be developed, but temafloxacin merits clinical evaluation.,B-Lactamase production and concomitant resistance to many ,B-lactams are usually encountered in the Bacteroides fragilis group but have been increasingly reported in other anaerobic gram-negative rods (2,6,7,13,14). We have examined the susceptibilities of 304 B. fragilis strains; 171 non-B. fragilis group Bacteroides, Prevotella, and Porphyromonas species (142 were P-lactamase positive); and 65 Fusobacterium species (50 were 1-lactamase positive) to amoxicillin, amoxicillin-BRL 42715 (a potent new ,B-lactamase inhibitor [8,9,17,23]), amoxicillin-clavulanate, temafloxacin (10,11,16,19), and clindamycin.Organisms were selected from clinical isolates collected over the past 4 years from diverse sources as previously described (2-6, 13, 14). Prior to being tested, strains were identified (1, 12, 20) as described previously. P-Lactamase production was tested by the nitrocefin disk method (BBL Microbiology Systems, Cockeysville, Md.) (4). MICs of amoxicillin, amoxicillin-clavulanate, amoxicillin-BRL 42715 (SmithKline Beecham Pharmaceuticals, Brockham Park, Betchworth, United Kingdom), temafloxacin (Abbott Laboratories, Chicago, Ill.), and clindamycin (The Upjohn Co., Kalamazoo, Mich.) were determined by agar dilution (2) extracts were standardized to contain similar units of activity against nitrocefin.In Tables 1 and 2, percent susceptibility rates of amoxicillin with and without inhibitors are presented at breakpoints of 2.0, 4.0, and 8.0 ,ugIml, respectively. Susceptibility data for ,B-lactamase-producing strains are shown in Table 1. Against all 3-lactamase-positive strains, addition of BRL 42715 to amoxicillin lowered the MICs for 50 and 90% of the strains tested (MlC50 and MIC90, respectively) from 32 and 256 to 0.25 and 2 ,ug/ml, respectively, and 99% of the strains were susceptible at all three amoxicillin breakpoints (27% of the strains were susceptible to amoxicillin at the NCCLS breakpoint of 4 ,ug/ml). Addition of clavulanate to amoxicillin lowered the MIC50 and MIC90 to 0.5 and 2.0 ,ug/ml, respectively, with 97% of the strains susceptible at the NCCLS amoxicillin breakpoint of 8 ,ug/ml (18). Temafloxacin and clindamycin showed good activity against 13-lactamase-producing strains (95 and 98%, respectively, were susceptible at .4 ,ug/ml), but clustering near the breakpoint was seen with both compounds.All ,B-lactamase-negative strains were susceptible to amoxicillin, temafloxacin, and clindamycin (Table 2), and many were susceptible to the...