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|Abstract:||Bacterial persisters are phenotypic variants with an extraordinary capacity to tolerate antibiotics, and they are hypothesized to be a main cause of chronic and relapsing infections. Recent evidence has suggested that the metabolism of persisters can be targeted to develop therapeutic counter-measures; however, knowledge of persister metabolism remains limited due to difficulties associated with isolating these rare and transient phenotypic variants. By using a technique to measure persister catabolic activity, which is based on the ability of metabolites to enable aminoglycoside (AG) killing of persisters, we investigated the role of seven global transcriptional regulators (ArcA, Cra, CRP, DksA, FNR, Lrp, and RpoS) on persister metabolism. We found that removal of CRP resulted in a loss of AG potentiation in persisters for all metabolites tested. These results highlight a central role for cAMP/CRP in persister metabolism, as its perturbation can significantly diminish the metabolic capabilities of persisters, and effectively eliminate the ability of AGs to eradicate these troublesome bacteria.|
|Electronic Publication Date:||23-Feb-2015|
|Citation:||Mok, Wendy WK, Orman, Mehmet A, Brynildsen, Mark P. (2015). Impacts of Global Transcriptional Regulators on Persister Metabolism. Antimicrobial Agents and Chemotherapy, 59 (5), 2713 - 2719. doi:10.1128/AAC.04908-14|
|Pages:||2713 - 2719|
|Type of Material:||Journal Article|
|Journal/Proceeding Title:||Antimicrobial Agents and Chemotherapy|
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