ACTIVITY OF MERSACIDIN, A NOVEL PEPTIDE, COMPARED WITH THAT OF VANCOMYCIN, TEICOPLANIN, AND DAPTOMYCIN

Mersacidin, a new peptide antibiotic, was four- to eightfold less active (MIC for 90% of isolates, 8-mu-g/ml) than vancomycin, teicoplanin, or daptomycin against Staphylococcus aureus. Coagulase-negative staphylococci were inhibited by 8-mu-g/ml, and the MICs of mersacidin for hemolytic streptococci and Streptococcus pneumoniae were 4 to 8-mu-g/ml. The mersacidin MICs for anaerobic organisms were as follows: Clostridium perfringens, 4-mu-g/ml; Propionibacterium acnes, 8-mu-g/ml; peptococci, 1-mu-g/ml; and peptostreptococci, 8-mu-g/ml. Mersacidin had no activity against members of the family Enterobacteriaceae, Neisseria and Haemophilus species, or Pseudomonas aeruginosa. The size of the inoculum, the pH of the assay (5.5 to 7.5), the type of medium, and the anaerobic conditions had minimal effects on the MICs and MBCs of mersacidin. Overall, mersacidin proved less active than available glycopeptides and peptolides.