In Vitro Activity of Antimicrobial Agents on Legionnaires Disease Bacterium
AUTOR(ES)
Thornsberry, Clyde
RESUMO
Six isolates of Legionnaires disease bacteria were tested for their susceptibility to 22 antimicrobial agents. The most active agent was rifampin (minimal inhibitory concentration, ≤0.01 μg/ml). On the basis of minimal inhibitory concentration breakpoints that have been used to categorize susceptibility for most of these drugs, the organisms were susceptible to rifampin, cefoxitin, erythromycin, the aminoglycosides, minocycline and doxycycline, chloramphenicol, ampicillin, penicillin G, carbenicillin, colistin, and sulfamethoxazole-trimethoprim (19:1 ratio); sensitive to intermediate in susceptibility to tetracycline, methicillin, cefamandole, cephalothin, and clindamycin; and resistant to vancomycin. More clinical data must be obtained before an optimal therapeutic regimen can be recommended.
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=352188Documentos Relacionados
- In vivo susceptibility of the Legionnaires disease bacterium to ten antimicrobial agents.
- Exotoxin activity associated with the Legionnaires disease bacterium.
- Identification of diaminopimelic acid in the Legionnaires disease bacterium.
- Transposition of bacteriophage Mu in the Legionnaires disease bacterium.
- Activity of eight antimicrobial agents in vitro against N. Gonorrhoeae.