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Showing papers by "Robert C. Moellering published in 1986"


Journal ArticleDOI
TL;DR: The in vitro activity of LY 146032 was comparable to that of vancomycin against most streptococci, but the latter demonstrated greater potency against Streptococcus faecium and penicillin-resistant strains of pneumococci and viridans group strePTococci.
Abstract: The in vitro activity of LY 146032, a cyclic lipopeptide antibiotic belonging to the class of agents designated A21978C, was compared with those of vancomycin, cefpirome, cefotaxime, and clindamycin against selected gram-positive bacteria. The new drug inhibited all staphylococcal isolates, including methicillin-resistant strains, at concentrations of less than or equal to 1.0 microgram/ml. The activity of LY 146032 was comparable to that of vancomycin against most streptococci, but the latter demonstrated greater potency against Streptococcus faecium and penicillin-resistant strains of pneumococci and viridans group streptococci. LY 146032 was markedly less active than vancomycin against Listeria monocytogenes (MICs for 90% of strains tested, 16 and 1.0 microgram/ml, respectively). The activity of LY 146032 was enhanced as the concentration of calcium in the test medium was increased. MBCs were within eightfold of the MIC for each of 12 strains tested. In a rat model of enterococcal endocarditis, the administration of LY 146032 resulted in increased survival and a reduction in the bacterial titer within cardiac vegetations compared with untreated control animals.

172 citations


Journal Article
TL;DR: Combinations of beta-lactams with aminoglycosides are widely used in the therapy of infections but usually result in synergism or indifference and very rarely in antagonism.

21 citations



Journal ArticleDOI
TL;DR: The role of Aminoglycosidic aminocyclitols and the newer beta-lactam antibiotics are particularly valuable in the management of hospital-acquired infections.

6 citations


Journal ArticleDOI
TL;DR: The in vitro activity of CI-934, a new quinolone antimicrobial, was compared with that of ciprofloxacin against selected gram-positive bacteria and, with the exception of Streptococcus faecium, all isolates were inhibited.

5 citations