4.5 Article

Impacts of Metabolism and Organic Acids on Cell Wall Composition and Pseudomonas aeruginosa Susceptibility to Membrane Active Antimicrobials

期刊

ACS INFECTIOUS DISEASES
卷 7, 期 8, 页码 2310-2323

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsinfecdis.1c00002

关键词

antimicrobial susceptibility testing; NMR metabolomics; colistin

资金

  1. Wellcome Trust [FC001029]
  2. British Heart Foundation
  3. Francis Crick Institute - Cancer Research UK [FC001029]
  4. U.K. Medical Research Council [FC001029]
  5. Health Schools Studentship - EPSRC [EP/M50788X/1]
  6. MRC Proximity to Discovery: Industry Engagement Fund [MC_PC_16074]
  7. King's Health Partners R&D Challenge rapid fund
  8. Wellcome Trust
  9. MRC [MC_PC_16074] Funding Source: UKRI

向作者/读者索取更多资源

Reliable antimicrobial susceptibility testing is crucial in clinical antibiotic therapy decisions and new antibiotic development. This study investigated the response of Escherichia coli and Pseudomonas aeruginosa to different growth media using NMR metabolomics and electron microscopy, to determine metabolic strategies and susceptibility to antimicrobials. The results showed that different media can affect the metabolic strategies of bacteria and their susceptibility to antimicrobial drugs.
Reliable antimicrobial susceptibility testing is essential in informing both clinical antibiotic therapy decisions and the development of new antibiotics. Mammalian cell culture media have been proposed as an alternative to bacteriological media, potentially representing some critical aspects of the infection environment more accurately. Here, we use a combination of NMR metabolomics and electron microscopy to investigate the response of Escherichia coli and Pseudomonas aeruginosa to growth in differing rich media to determine whether and how this determines metabolic strategies, the composition of the cell wall, and consequently susceptibility to membrane active antimicrobials including colistin and tobramycin. The NMR metabolomic approach is first validated by characterizing the expected E. coli acid stress response to fermentation and the accompanying changes in the cell wall composition, when cultured in glucose rich mammalian cell culture media. Glucose is not a major carbon source for P. aeruginosa but is associated with a response to osmotic stress and a modest increase in colistin tolerance. Growth of P. aeruginosa in a range of bacteriological media is supported by consumption of formate, an important electron donor in anaerobic respiration. In mammalian cell culture media, however, the overall metabolic strategy of P. aeruginosa is instead dependent on consumption of glutamine and lactate. Formate doping of mammalian cell culture media does not alter the overall metabolic strategy but is associated with polyamine catabolism, remodelling of both inner and outer membranes, and a modest sensitization of P. aeruginosa PAO1 to colistin. Further, in a panel of P. aeruginosa isolates an increase between 2- and 3-fold in sensitivity to tobramycin is achieved through doping with other organic acids, notably propionate which also similarly enhances the activity of colistin. Organic acids are therefore capable of nonspecifically influencing the potency of membrane active antimicrobials.

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