4.7 Article

Double deletion of cpxR and tolC significantly increases the susceptibility of Salmonella enterica serovar Typhimurium to colistin

Journal

JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY
Volume 76, Issue 12, Pages 3168-3174

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/jac/dkab332

Keywords

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Funding

  1. National Natural Science Foundation of China [32072913]

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This study revealed that the double deletion of cpxR and tolC significantly increases the susceptibility of S. Typhimurium to colistin. The molecular mechanisms underlying this phenomenon were elucidated through transcriptomic analysis.
Background: The increasing use of colistin causes a serious breach in our last line of defence against MDR Gram-negative pathogens. Our previous study showed that CpxR overexpression increases the susceptibility of acrB and cpxR double-deleted Salmonella enterica serovar Typhimurium to colistin. Objectives: To identify the mechanism of CpxAR and efflux pumps that synergistically enhance the susceptibility of S. Typhimurium to colistin. Methods: A series of cpxR- and tolC-deleted mutants and a cpxR-complemented strain from a multidrug-susceptible standard strain of S. Typhimurium (JS) were generated in our previous study. Herein, we investigated the susceptibility of these strains to colistin through the broth microdilution method, time-kill curves and survival assays. Growth curves were measured by OD600 in LB broth, tryptone-soy broth (TSB) and M9-glucose (0.2%) minimal media. Finally, molecular mechanisms underlying the mode of action were elucidated by transcriptomic analysis. Results: We found that in contrast to JS (0.8mg/L), the MIC of colistin for JS Delta tolC::kan showed a 16-fold decrease (0.05mg/L). Notably, JS Delta cpxR Delta tolC and JS Delta cpxR Delta tolC/pcpxR were associated with a 256-fold decrease (0.0031mg/L) compared with JS. Growth curves identified that JS Delta cpxR Delta tolC and JS Delta cpxR Delta tolC/pcpxR displayed a markedly lower growth rate and poorer adaptability. In addition, time-kill curves and survival assays showed that JS Delta cpxR Delta tolC and JS Delta cpxR Delta tolC/pcpxR were more susceptible to colistin. Lastly, double deletion of cpxR and tolC enhanced oxidative damage through promoting oxidative phosphorylation, the tricarboxylic acid (TCA) cycle and trimethylamine N-oxide (TMAO) respiration. Conclusions: Our findings revealed that double deletion of cpxR and tolC significantly increases the susceptibility of S. Typhimurium to colistin.

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