Isolates with reduced susceptibility to third generation cephalosporins were subjected to phenotypic detection of ESBL production by using cefotaxime (CTX) and ceftazidime (CAZ) discs and double-disk synergy (DDS) method as recommended by the Clinical and Laboratory Standards Institute [14 ]. AmpC production was detected using cefoxitin alone and in combination with boronic acid and confirmation was done by three-dimensional disk method. Isolates with reduced susceptibility to cefoxitin were subjected to a modified three-dimensional extract test to confirm AmpC production [15 ].
Antimicrobial agent discs
Antimicrobial agent discs are laboratory equipment used to test the susceptibility of microorganisms to various antimicrobial agents. These discs are impregnated with known concentrations of antimicrobial agents and are placed on agar plates inoculated with the target microorganism. The size of the resulting zone of inhibition around the disc indicates the sensitivity or resistance of the microorganism to the antimicrobial agent.
Lab products found in correlation
2 protocols using antimicrobial agent discs
Antimicrobial Susceptibility Testing Protocol
Isolates with reduced susceptibility to third generation cephalosporins were subjected to phenotypic detection of ESBL production by using cefotaxime (CTX) and ceftazidime (CAZ) discs and double-disk synergy (DDS) method as recommended by the Clinical and Laboratory Standards Institute [14 ]. AmpC production was detected using cefoxitin alone and in combination with boronic acid and confirmation was done by three-dimensional disk method. Isolates with reduced susceptibility to cefoxitin were subjected to a modified three-dimensional extract test to confirm AmpC production [15 ].
Disc Diffusion Antibiotic Susceptibility of F. psychrophilum
1, LP0011, Oxoid, UK) (MHA) and 5% foetal calf serum (FCS; Gibco, Fisher chemicals, UK) and plates were incubated at 15 o C for 68 -72 h. Antimicrobial agent discs (Oxoid, Basingstoke, UK) containing 10 µg amoxicillin (AMOX10), 5 µg enrofloxacin (ENRO5), 30 µg florfenicol (FFN30), 2 µg oxolinic acid (OXO2), 30 µg oxytetracycline (OTC30) and 25 µg trimethoprim/sulphamethoxazole (SXT25) were employed.
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