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Susceptibility of Yersinia pestis to novel and conventional antimicrobial agents
John Frean1, Keith P Klugman, Lorraine Arntzen
1National Institute for Communicable Diseases, National Health Laboratory Service, Johannesburg, South Africa.
Objectives:
To determine the susceptibility of southern African strains of Yersinia pestis to novel as well as conventional antimicrobial agents.
Materials And Methods:
The MICs of 28 strains of Yersinia pestis from a southern African plague focus were determined by agar dilution.
Results:
The most active agents were cefditoren and the fluoroquinolones, both conventional and novel. The in vitro activity of macrolides was poor against this member of the Enterobacteriaceae.
Conclusion:
Further investigation of the novel quinolones olamufloxacin (HSR 903) and ABT 492 in animal models of plague would seem to be justified.
Insights
Southern African Yersinia pestis strains showed susceptibility to cefditoren and fluoroquinolones. Novel fluoroquinolones like olamufloxacin warrant further plague research.
Area of Science:
- Microbiology
- Infectious Diseases
- Antimicrobial Resistance
Background:
- Yersinia pestis is the causative agent of plague.
- Antimicrobial susceptibility of Yersinia pestis strains varies geographically.
- Southern Africa is a significant plague focus.
Purpose of the Study:
- To assess the antimicrobial susceptibility of southern African Yersinia pestis strains.
- To evaluate both novel and conventional antimicrobial agents against these strains.
Main Methods:
- Agar dilution method was employed.
- Minimum Inhibitory Concentrations (MICs) were determined.
- 28 Yersinia pestis strains from a southern African plague focus were tested.
Main Results:
- Cefditoren and fluoroquinolones (conventional and novel) demonstrated the highest in vitro activity.
- Macrolides exhibited poor activity against these Yersinia pestis strains.
- Enterobacteriaceae susceptibility patterns were observed.
Conclusions:
- Novel fluoroquinolones, specifically olamufloxacin (HSR 903) and ABT 492, show promise.
- Further investigation in animal models of plague is recommended for these novel agents.
- Cefditoren and fluoroquinolones are potential therapeutic options.
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