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

IF 2.1 3区 生物学 Q3 BIOCHEMICAL RESEARCH METHODS Proteome Science Pub Date : 2023-09-28 DOI:10.1186/s12953-023-00217-6
Hong Loan Ngo, Thuc Quyen Huynh, Nguyen Bao Vy Tran, Ngoc Hoa Binh Nguyen, Thi Hang Tong, Thi Truc Ly Trinh, Van Dung Nguyen, Prem Prakash Das, Teck Kwang Lim, Qingsong Lin, Thi Thu Hoai Nguyen
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Abstract

Background: 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.

Methods: 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).

Results: 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.

Conclusion: 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.

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头孢他啶和美罗培南暴露的铜绿假单胞菌ATCC 9027的蛋白质组学分析。
背景:铜绿假单胞菌以其固有的抵抗多种抗生素的能力而闻名,因此使治疗变得复杂。因此,了解病原体对抗生素的反应对于开发新的治疗方法很重要。本研究研究了铜绿假单胞菌对常用抗假单胞菌抗生素头孢他啶(Caz)和美罗培南(Mem)的蛋白质组学反应。方法:将抗生素敏感菌株铜绿假单胞菌ATCC 9027暴露于Caz或Mem的亚MIC值下14天,获得E1菌株,然后在无抗生素环境中培养10天,获得E2菌株。使用相对和绝对定量同量标签(iTRAQ)与纳米LC-MS/MS合作,鉴定并比较分析了初始菌株和E1、E2菌株的蛋白质组。定量逆转录聚合酶链式反应(qRT-PCR)证实了上调和下调的蛋白。结果:总的来说,在Caz和Mem暴露的菌株中分别鉴定出1039和1041个蛋白。在抗生素暴露后,存在7-10%的上调(Caz:71,Mem:85)和下调(Caz:106,Mem:69)蛋白(1.5倍变化截止值)。对于Caz和Mem,DEP主要参与代谢过程、膜、毒力、蛋白质合成和抗生素耐药性,其中参与抗生素耐药性的蛋白质倾向于上调,而参与蛋白质合成和代谢过程的蛋白质则下调。注意到的蛋白质包括在两种抗生素暴露菌株中上调的β-内酰胺酶AmpC和下调的OprD。此外,Caz暴露菌株中与生物膜形成相关的蛋白TssC1和Hcp1以及Mem暴露菌株中的膜/周质蛋白Azu和PagL被发现显著下调。qRT-PCR结果证实了AmpC、Hcp1和OprD蛋白的表达变化。结论:铜绿假单胞菌暴露于Caz和Mem的亚MIC值导致其蛋白质组发生约10%的变化。不仅证实在抗生素耐药性机制中发挥作用的蛋白质改变了它们的表达,而且毒力相关蛋白质也改变了。Caz和Mem反应均涉及AmpC的上调和OprD的下调。TssC1和Hcp1负责Caz反应,而Azu和PagL更有可能参与Mem反应。
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来源期刊
Proteome Science
Proteome Science 生物-生化研究方法
CiteScore
2.90
自引率
0.00%
发文量
17
审稿时长
4.5 months
期刊介绍: Proteome Science is an open access journal publishing research in the area of systems studies. Proteome Science considers manuscripts based on all aspects of functional and structural proteomics, genomics, metabolomics, systems analysis and metabiome analysis. It encourages the submissions of studies that use large-scale or systems analysis of biomolecules in a cellular, organismal and/or environmental context. Studies that describe novel biological or clinical insights as well as methods-focused studies that describe novel methods for the large-scale study of any and all biomolecules in cells and tissues, such as mass spectrometry, protein and nucleic acid microarrays, genomics, next-generation sequencing and computational algorithms and methods are all within the scope of Proteome Science, as are electron topography, structural methods, proteogenomics, chemical proteomics, stem cell proteomics, organelle proteomics, plant and microbial proteomics. In spite of its name, Proteome Science considers all aspects of large-scale and systems studies because ultimately any mechanism that results in genomic and metabolomic changes will affect or be affected by the proteome. To reflect this intrinsic relationship of biological systems, Proteome Science will consider all such articles.
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