Affiliation:
1. Department of Medicine, Montefiore Hospital and University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania 15213
Abstract
The in vitro activity of netilmicin (Sch 20569), a new semisynthetic derivative of gentamicin, was compared with that of gentamicin and amikacin. One hundred and ninety-two clinical isolates of
Enterobacteriaceae, Pseudomonas aeruginosa
, and
Staphylococcus aureus
were tested using both agar and broth dilution techniques. Netilmicin was comparable to gentamicin, with the following exceptions: (i) for
Serratia marcescens
and
P. aeruginosa
, gentamicin was more active than netilmicin; (ii) all strains of
Escherichia coli, Klebsiella, Enterobacter, Proteus mirabilis
, and
Citrobacter freundii
, which were resistant to gentamicin, were susceptible to netilmicin; (iii) some strains of
S. marcescens
, indole-positive
Proteus
, and
Providencia
, which were resistant to gentamicin, were susceptible to netilmicin. Netilmicin was more active than amikacin for all
Enterobacteriaceae
and
S. aureus
and equal to amikacin in activity against gentamicin-susceptible strains of
P. aeruginosa
. All strains of
P. aeruginosa
, resistant to gentamicin, were also resistant to netilmicin but were susceptible to amikacin. Minimal inhibitory concentrations (MICs) obtained with broth and agar showed no significant differences except for
P. mirabilis
, where broth MICs were twofold greater than agar MICs, and for
P. aeruginosa
, where agar MICs were twofold higher than broth MICs. The minimal bactericidal concentration (MBC) was either identical to or within one twofold dilution of the MIC for the strains tested. A 100-fold increase in inoculum size produced less increase in MIC and MBC with netilmicin than with gentamicin or amikacin.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Cited by
24 articles.
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