Susceptibility of Helicobacter pylori to mupirocin, oxazolidinones, quinupristin/dalfopristin and new quinolones

Citation
Jeg. Sanchez et al., Susceptibility of Helicobacter pylori to mupirocin, oxazolidinones, quinupristin/dalfopristin and new quinolones, J ANTIMICRO, 46(2), 2000, pp. 283-285
Citations number
10
Categorie Soggetti
Pharmacology,Microbiology
Journal title
Journal of antimicrobial chemotherapy
ISSN journal
03057453 → ACNP
Volume
46
Issue
2
Year of publication
2000
Pages
283 - 285
Database
ISI
SICI code
Abstract
The in vitro activities of mupirocin, quinupristin/dalfopristin, linezolid, eperezolid, sitafloxacin, clinafloxacin, moxifloxacin, amoxycillin, metron idazole and clarithromycin were tested at pH 7.4 against 57 strains of Heli cobacter pylori. The most active agents (mupirocin, sitafloxacin and clinaf loxacin) were also tested for activity at pH 5.4 against the same strains, Mupirocin was very active at pH 7.4 and 5.4 (MIC90 0.25 and 0.12 mg/L, resp ectively). Quinupristin/dalfopristin, linezolid and eperezolid had low acti vity (MIC90 4, 8 and 4 mg/L, respectively), Sitafloxacin (MIC90 less than o r equal to 0.008 mg/L) was the most active fluoroquinolone, while clinaflox acin (MIC90 0.12 mg/L) and moxifloxacin (MIC90 2 mg/L) were least active.