2022
DOI: 10.1021/acs.jproteome.1c00936
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Impact of Carbon Source Supplementations on Pseudomonas aeruginosa Physiology

Abstract: Pseudomonas aeruginosa is an opportunistic pathogen highly resistant to a wide range of antimicrobial agents, making its infections very difficult to treat. Since microorganisms need to perpetually adapt to their surrounding environment, understanding the effect of carbon sources on P. aeruginosa physiology is therefore essential to avoid increasing drug-resistance and better fight this pathogen. By a global proteomic approach and phenotypic assays, we investigated the impact of various carbon source supplemen… Show more

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Cited by 8 publications
(5 citation statements)
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References 72 publications
(129 reference statements)
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“…This can in turn have a profound impact on their growth rate, virulence, phenotypes, and resistance to antibiotics [9,[67][68][69][70]. Earlier studies have described the role of carbon sources in the metabolism of P. aeruginosa [71][72][73][74]. Our study highlights the role of malonate as a sole carbon source in inducing a global stress response in P. aeruginosa.…”
Section: Discussionmentioning
confidence: 77%
“…This can in turn have a profound impact on their growth rate, virulence, phenotypes, and resistance to antibiotics [9,[67][68][69][70]. Earlier studies have described the role of carbon sources in the metabolism of P. aeruginosa [71][72][73][74]. Our study highlights the role of malonate as a sole carbon source in inducing a global stress response in P. aeruginosa.…”
Section: Discussionmentioning
confidence: 77%
“…This might be that both media rich in various sugars as a carbon source (Supplementary Table S2) resulted in alteration of bacterial cell wall structure. It is well-known that physiological microorganisms (cell wall structure, virulence, biofilm formation, or antibiotic resistance) are relevant on carbon sources for growth such reports in Pseudomonas aeruginosa PA14 49 and in Candida albicans 50 . The proteomic analysis should be evaluated to describe more details in future.…”
Section: Resultsmentioning
confidence: 99%
“…The supernatants collected between 2 h and 12 h and at 24 h and 48 h of incubation, were diluted 2- and 10-fold, respectively. LC–MS/MS analytical conditions were adapted from methods previously described ( Déziel et al, 2000 ; Bazire et al, 2005 ; Sauvage et al, 2022 ). Analysis of biosurfactants was performed with a 1,290 Infinity II UHPLC system coupled to a 6545XT Advance-Bio Q-TOF mass spectrometer (Agilent Technologies, United States).…”
Section: Methodsmentioning
confidence: 99%