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Microbiological characterization of everninomicins B and D
Antimicrobial Agents and Chemotherapy
|September 1, 1974
Summary
Everninomicins B and D show potent antibiotic activity against gram-positive bacteria and Neisseria. These compounds exhibit bacteriostatic effects and merit further investigation as potential therapeutic agents.
Area of Science:
- Microbiology
- Pharmacology
- Antibiotic Discovery
Background:
- Everninomicins B and D are antibiotic compounds produced by Micromonospora.
- These antibiotics are part of a complex of antimicrobial substances.
Purpose of the Study:
- To evaluate the in vitro activity of Everninomicins B and D.
- To compare their potency against common antibiotics like penicillin G and chloramphenicol.
- To assess the development of resistance and cross-resistance to these compounds.
Main Methods:
- In vitro susceptibility testing against various bacterial strains including gram-positive bacteria, Neisseria, and Bacteroides.
- Determination of bacteriostatic activity.
- Laboratory selection of resistant mutants from susceptible staphylococci.
- Assay of antimicrobial activity under varied conditions (media, growth, inoculum size, serum presence).
Main Results:
- Everninomicins B and D demonstrated high in vitro activity against gram-positive bacteria, Neisseria, and Bacteroides.
- Activity was greater than chloramphenicol but less than penicillin G against susceptible strains.
- Compounds were bacteriostatic, except against group A streptococci; no activity against facultative anaerobic gram-negative bacilli.
- Resistant mutants were difficult to select and showed no cross-resistance to existing antimicrobial agents.
- Antibacterial activity was reduced by serum or increased inoculum size.
- Everninomicin B was more potent against gonococci and group A streptococci; Everninomicin D was more potent against enterococci.
Conclusions:
- Everninomicins B and D possess significant in vitro antibacterial activity.
- The difficulty in selecting resistant mutants suggests a low propensity for resistance development.
- Their high activity and lack of cross-resistance warrant further investigation as potential therapeutic agents.