Publication | Open Access
<i>In Vitro</i> Susceptibility of <i>Chlamydia pecorum</i> to Macrolides, Tetracyclines, Quinolones and β‐Lactam
22
Citations
8
References
1998
Year
Antibacterial AgentsAntimicrobial SusceptibilityHealth SciencesAntibioticsMedicineAntibiotic AdjuvantVitro SusceptibilityPharmacologyEffective DrugsChlamydia PecorumAntibacterial AgentAntimicrobial ChemotherapyMicrobiologyAntibacterial MechanismsAnti-infective AgentsClinical MicrobiologyAntimicrobial ResistanceDrug Resistance
The in vitro susceptibility of Chlamydia pecorum to two macrolides (clarithromycin and erythromycin), two tetracyclines (doxycycline and minocycline), two quinolones (ofloxacin and ciprofloxacin) and one beta-lactam (ampicillin) was determined. The MICs were 0.004 to 0.008 microg/ml for clarithromycin, 0.008 to 0.031 microg/ml for doxycycline and minocycline, 0.063 to 0.125 microg/ml for erythromycin, 0.25 to 0.5 microg/ml for ofloxacin and 0.25 to 1.0 microg/ml for ciprofloxacin. The MIC for ampicillin was greater than 1,024 microg/ml. The results show clarithromycin and doxycycline are the two most effective drugs against C. pecorum.
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