Affiliation:
1. Departments of Pathology and Laboratory Medicine1 and
2. Medicine,2 University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104-4283
Abstract
ABSTRACT
The activities of HMR 3647, HMR 3004, erythromycin, clarithromycin, and levofloxacin for 97
Legionella
spp. isolates were determined by microbroth dilution susceptibility testing. Growth inhibition of two
Legionella pneumophila
strains grown in guinea pig alveolar macrophages was also determined. The concentrations required to inhibit 50% of strains tested were 0.06, 0.02, 0.25, 0.03, and 0.02 μg/ml for HMR 3647, HMR 3004, erythromycin, clarithromycin, and levofloxacin, respectively. BYEα broth did not significantly inhibit the activities of the drugs tested, as judged by the susceptibility of the control
Staphylococcus aureus
strain; however, when
Escherichia coli
was used as the test strain, levofloxacin activity tested in BYEα broth was fourfold lower. HMR 3647, HMR 3004, erythromycin, and clarithromycin (0.25 and 1 μg/ml) reduced bacterial counts of two
L. pneumophila
strains grown in guinea pig alveolar macrophages by 0.5 to 1 log
10
, but regrowth occurred over a 2-day period. HMR 3647, erythromycin, and clarithromycin appeared to have equivalent intracellular activities which were solely static in nature. HMR 3004 was more active than all drugs tested except levofloxacin. In contrast, levofloxacin (1 μg/ml) was bactericidal against intracellular
L. pneumophila
and significantly more active than the other drugs tested. Therapy studies with HMR 3647 and erythromycin were performed in guinea pigs with
L. pneumophila
pneumonia. When HMR 3647 was given (10 mg/kg of body weight) by the intraperitoneal route to infected guinea pigs, mean peak plasma levels were 1.4 μg/ml at 0.5 h and 1.0 μg/ml at 1 h postinjection. The terminal half-life phase of elimination from plasma was 1.4 h. All 16
L. pneumophila
-infected guinea pigs treated with HMR 3647 (10 mg/kg/dose given intraperitoneally once daily) for 5 days survived for 9 days after antimicrobial therapy, as did all 16 guinea pigs treated with the same dose of HMR 3647 given twice daily. Fourteen of 16 erythromycin-treated (30 mg/kg/dose given intraperitoneally twice daily) animals survived, whereas 0 of 12 animals treated with saline survived. HMR 3647 is effective against
L. pneumophila
in vitro, in infected macrophages, and in a guinea pig model of Legionnaires’ disease. HMR 3647 given once daily should be evaluated as a treatment for Legionnaires’ disease in humans.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Reference34 articles.
1. Agouridas
C.
Bonnefoy
A.
Chantot
J. F.
In vitro antibacterial activity of RU 004 a novel ketolide highly active against respiratory pathogens abstr. F158
Program and abstracts of the 35th Interscience Conference on Antimicrobial Agents and Chemotherapy.
1995
140
American Society for Microbiology
Washington D.C
2. Antibacterial activity of RU 64004 (HMR 3004), a novel ketolide derivative active against respiratory pathogens
3. The ketolide antibiotics HMR 3647 and HMR 3004 are active against Toxoplasma gondii in vitro and in murine models of infection
4. In vitro activity of the new ketolide HMR 3004 compared to an azalide and macrolides against Streptococcus pneumoniae and Haemophilus influenzae.;Barry A. L.;Eur. J. Clin. Microbiol. Infect. Dis.,1997
5. Bornstein
N.
Behr
H.
Brun
Y.
Fleurette
J. In vitro activity of RU 004 on Legionella species abstr. F166
Program and abstracts of the 35th Interscience Conference on Antimicrobial Agents and Chemotherapy.
1995
142
American Society for Microbiology
Washington D.C
Cited by
93 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献