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- Title
Molecular mechanisms of resistance to antibiotics in Bartonella bacilliformis.
- Authors
Silpak Biswas; Didier Raoult; Jean-Marc Rolain
- Abstract
: Objectives Bartonella bacilliformis is the aetiological agent of Carrions disease. Although ciprofloxacin, rifampicin and erythromycin have been successfully used in the treatment of the disease, failures and relapses have been reported. The objective of our study was to select in vitro mutants resistant to antibiotics in order to determine the frequency of mutations and to characterize the mechanism of resistance at the molecular level. : Methods Antibiotic-resistant mutants were selected by serial passages of bacteria on blood agar plates containing antibiotics. Candidate genes involved in resistance were amplified and sequenced and compared in order to look at mutations associated with antibiotic resistance. : Results Ciprofloxacin-, rifampicin- and erythromycin-resistant mutants were obtained after five, three and four passages, respectively. Conversely, no mutant was obtained with either gentamicin or doxycycline even after 16 passages. The ciprofloxacin mutant contained an amino acid change at position 87 (Asp → Asn) in its quinolone resistance-determining region of the DNA gyrase protein, whereas the rifampicin-resistant strain had an amino acid change at position 531 (Ser → Phe) in the rifampicin resistance-determining region of the rpoB gene. Similarly, the erythromycin-resistant mutant showed an A2058G mutation in the 23S rRNA gene. : Conclusions According with the current knowledge on the treatment of human bartonellosis, we believe that doxycycline in association with gentamicin may be the preferred regimen for the treatment of the acute and eruptive stages of Carrions disease, but clinical trials are warranted to support our findings.
- Subjects
ANTIBIOTICS; ERYTHROMYCIN; MACROLIDE antibiotics; BARTONELLA
- Publication
Journal of Antimicrobial Chemotherapy (JAC), 2007, Vol 59, Issue 6, p1065
- ISSN
0305-7453
- Publication type
Article
- DOI
10.1093/jac/dkm105