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Metabolomics,Unknown,Transcriptomics,Genomics,Proteomics

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Gene expression profiling of siderophore-drug resistant mutant of Pseudomonas aeruginosa PAO1

ABSTRACT: The aim of the experiment was to identify genes differentially expressed between the susceptible wild type strain P. aeruginosa PAO1 (PT5) and a mutant resistant to a drug-siderophore conjugate, in order to obtain information on the resistance mechanism(s). A mutant of PT5 able to grow at 4 mg/l BAL30072, a drug-siderophore conjugate, was selected in vitro . The susceptible wild type strain PT5 and the mutant (BAL6) were grown in LB medium and the mutant also in the presence of 4 mg/l BAL30072 to mid-exponential growth phase (OD600 =2) in triplicate cultures. RNA was extracted using the RNeasy Kit (Qiagen). A total of nine Affymterix P. aeruginosa arrays were hybridized (one for each replicate) under standard conditions.

ORGANISM(S): Pseudomonas aeruginosa

SUBMITTER: Olivier Schaad

PROVIDER: E-MTAB-1381 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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Involvement of Fe uptake systems and AmpC β-lactamase in susceptibility to the siderophore monosulfactam BAL30072 in Pseudomonas aeruginosa.

van Delden Christian C Page Malcolm G P MG Köhler Thilo T

Antimicrobial agents and chemotherapy 20130219 5

BAL30072 is a monosulfactam conjugated with an iron-chelating dihydroxypyridone moiety. It is active against Gram-negative bacteria, including multidrug-resistant Pseudomonas aeruginosa. We selected mutants with decreased susceptibilities to BAL30072 in P. aeruginosa PAO1 under a variety of conditions. Under iron-deficient conditions, mutants with overexpression of AmpC β-lactamase predominated. These mutants were cross-resistant to aztreonam and ceftazidime. Similar mutants were obtained after ...[more]

PMID: 23422914

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