Proteomic profiling of clinical and environmental strains of Pseudomonas aeruginosa
Autor: | Ganeswrei Rajasekaram, Hwa Chia Chai, Siew Mun Liew, S. D. Puthucheary, Kek Heng Chua |
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Rok vydání: | 2020 |
Předmět: |
0301 basic medicine
Proteomics Virulence Biology medicine.disease_cause Mass Spectrometry Microbiology 03 medical and health sciences 0302 clinical medicine Chitin binding Drug Resistance Multiple Bacterial Genetics medicine Environmental Microbiology Cluster Analysis Molecular Biology Gel electrophoresis Principal Component Analysis Pseudomonas aeruginosa Proteomic Profiling General Medicine Gene Expression Regulation Bacterial biology.organism_classification Multiple drug resistance 030104 developmental biology 030220 oncology & carcinogenesis Ornithine transport Bacteria |
Zdroj: | Molecular biology reports. 48(3) |
ISSN: | 1573-4978 |
Popis: | Pseudomonas aeruginosa is a ubiquitous bacterium, which is able to change its physiological characteristics in response to different habitats. Environmental strains are presumably less pathogenic than clinical strains and whether or not the clinical strains originate from the environment or through inter-host transmission remains poorly understood. To minimize the risk of infection, a better understanding of proteomic profiling of P. aeruginosa is necessary for elucidating the correlation between environmental and clinical strains. Based on antimicrobial susceptibility and patterns of virulence, we selected 12 clinical and environmental strains: (i) environmental, (ii) multidrug resistant (MDR) clinical and (iii) susceptible clinical strains. Whole-cell protein was extracted from each strain and subjected to two-dimensional differential gel electrophoresis (2-D DIGE) and liquid chromatography tandem mass spectrometry quadrupole time-of-flight (LC-MS QTOF). All 12 strains were clustered into 3 distinct groups based on their variance in protein expression. A total of 526 matched spots were detected and four differentially expressed protein spots (p < 0.05) were identified and all differential spots were downregulated in MDR strain J3. Upregulation of chitin binding and BON domain proteins was present in the environmental and some MDR strains, whereas the clinical strains exhibited distinct proteomic profiles with increased expression of serine protein kinase and arginine/ornithine transport ATP-binding proteins. Significant difference in expression was observed between susceptible clinical and MDR strains, as well as susceptible clinical and environmental strains. Transition from an environmental saprophyte to a clinical strain could alter its physiological characteristics to further increase its adaptation. |
Databáze: | OpenAIRE |
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