Proteomic analysis of ceftazidime and meropenem-exposed Pseudomonas aeruginosa ATCC 9027

• Published in: Proteome science Vol. 21; no. 1; pp. 1 - 15
• Main Authors: Ngo, Hong Loan, Huynh, Thuc Quyen, Tran, Nguyen Bao Vy, Nguyen, Ngoc Hoa Binh, Tong, Thi Hang, Trinh, Thi Truc Ly, Nguyen, Van Dung, Das, Prem Prakash, Lim, Teck Kwang, Lin, Qingsong, Nguyen, Thi Thu Hoai
• Format: Journal Article
• Language: English
• Published: London BioMed Central Ltd 28.09.2023; BioMed Central; BMC
• Subjects: Antibiotic resistance; Antibiotics; Beta lactamases; Biofilms; Ceftazidime; Cooperativity; DNA polymerases; Drug resistance; Drug resistance in microorganisms; Genes; iTRAQ; Membrane proteins; Meropenem; Minimum inhibitory concentration; Nosocomial infections; Pathogens; Protein biosynthesis; Proteins; Proteomes; Proteomics; Pseudomonas aeruginosa; Quantitative proteomics analysis; RNA-directed DNA polymerase; Virulence; β Lactamase; Canada
• ISSN: 1477-5956; 1477-5956
• DOI: 10.1186/s12953-023-00217-6

Pseudomonas aeruginosa is well known for its intrinsic ability to resist a wide range of antibiotics, thus complicates treatment. Thus, understanding the response of the pathogen to antibiotics is important for developing new therapies. In this study, proteomic response of P. aeruginosa to the commonly used anti-pseudomonas antibiotics, ceftazidime (Caz) and meropenem (Mem) was investigated. P. aeruginosa ATCC 9027, an antibiotic-susceptible strain, was exposed to sub-MIC values of antibiotics either Caz or Mem for 14 days to obtain E1 strains and then cultured in antibiotic-free environments for 10 days to obtain E2 strains. Proteomes of the initial and E1, E2 strains were identified and comparatively analyzed using isobaric tags for relative and absolute quantitation (iTRAQ) in cooperation with nano LC-MS/MS. Noted up and down-regulated proteins were confirmed with quantitative reverse transcriptase PCR (qRT-PCR). Overall, 1039 and 1041 proteins were identified in Caz and Mem-exposed strains, respectively. Upon antibiotic exposure, there were 7-10% up-regulated (Caz: 71, Mem: 85) and down-regulated (Caz: 106, Mem: 69) proteins (1.5-fold change cut-off). For both Caz and Mem, the DEPs were primarily the ones involved in metabolic process, membrane, virulence, protein synthesis, and antibiotic resistance in which proteins involved in antibiotics resistance tended to be up-regulated while proteins involved in protein synthesis and metabolic process were down-regulated. Noted proteins included beta-lactamase AmpC which was up-regulated and OprD which was down-regulated in both the antibiotic-exposed strains. Besides, biofilm formation related proteins TssC1 and Hcp1 in Caz- exposed strains and the membrane/ periplasmic proteins Azu and PagL in Mem-exposed strains were found significantly down-regulated. qRT-PCR results confirmed the expression change of AmpC, Hcp1 and OprD proteins. Exposure of Pseudomonas aeruginosa to sub-MIC values of Caz and Mem resulted in around 10% change in its proteome. Not only proteins with confirmed roles in antibiotic resistance mechanisms changed their expression but also virulence- associated proteins. Both Caz and Mem response involved up-regulation of AmpC and down-regulation of OprD. While TssC1 and Hcp1 were responsible for Caz response, Azu and PagL were more likely involved in Mem response.