Abstract
Chronic infections caused by persistent pathogens represent an important health problem. Here, we establish a simple practical mouse Salmonella infection model for identifying bacterial maintenance functions that are essential for persistency. In this model, a substantial fraction of Salmonella survived even several days of treatment with a potent fluoroquinolone antibiotic indicating stringency of the model. Evaluation of twelve metabolic defects revealed dramatically different requirements for Salmonella during persistency as compared to acute infections. Disrupted synthesis of unsaturated/cyclopropane fatty acids was the only defect that resulted in rapid Salmonella clearance suggesting that this pathway might contain suitable targets for antimicrobial chemotherapy of chronic infection. © 2012 Barat et al.
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CITATION STYLE
Barat, S., Steeb, B., Mazé, A., & Bumann, D. (2012). Extensive in vivo resilience of persistent Salmonella. PLoS ONE, 7(7). https://doi.org/10.1371/journal.pone.0042007
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