In vitro antimicrobial susceptibilities of penicillinase-producing and non-penicillinase-producing strains of Neisseria gonorrhoeae isolated in Durban, South Africa
Open Access
- 1 November 1984
- journal article
- research article
- Published by American Society for Microbiology in Antimicrobial Agents and Chemotherapy
- Vol. 26 (5) , 770-772
- https://doi.org/10.1128/aac.26.5.770
Abstract
The in vitro susceptibilities of 22 penicillinase-producing and 32 non-penicillinase-producing strains of Neisseria gonorrhoeae to 13 antimicrobial agents, including the new semisynthetic penicillins and cephalosporins, are reported. Ceftriaxone, ceftazidime, and cefotaxime were the most active agents tested; none of them had an MIC of greater than 0.03 micrograms/ml. Amoxycillin plus clavulanic acid and temocillin also showed good activity against both strains of gonococci.Keywords
This publication has 8 references indexed in Scilit:
- The emergence of penicillinase-producing strains of Neisseria gonorrhoeae in Durban.1984
- Penicillinase-producing Neisseria gonorrhoeae isolates from different localities in south east Asia. Susceptibility to 15 antibiotics.Sexually Transmitted Infections, 1983
- In vitro susceptibility and cross-resistance of South African isolates of Neisseria gonorrhoeae to 14 antimicrobial agentsAntimicrobial Agents and Chemotherapy, 1982
- BRL 17421, a novel beta-lactam antibiotic, highly resistant to beta-lactamases, giving high and prolonged serum levels in humansAntimicrobial Agents and Chemotherapy, 1981
- Neisseria gonorrhoeae strains isolated in Hong Kong: in vitro susceptibility to 13 antibioticsAntimicrobial Agents and Chemotherapy, 1981
- In vitro antimicrobial activity of piperacillin and seven other β-lactam antibiotics against Neisseria gonorrhoeae and Haemophilus influenzae, including β-lactamase producing strainsJournal of Antimicrobial Chemotherapy, 1979
- Antibiotic Resistance in Neisseria GonorrhoeaeMedical Clinics of North America, 1972
- Novel Method for Detection of β-Lactamases by Using a Chromogenic Cephalosporin SubstrateAntimicrobial Agents and Chemotherapy, 1972