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Multiplexed activity-based protein profiling of the human pathogen Aspergillus fumigatus reveals large functional changes upon exposure to human serum.
- Source :
-
The Journal of biological chemistry [J Biol Chem] 2012 Sep 28; Vol. 287 (40), pp. 33447-59. Date of Electronic Publication: 2012 Aug 03. - Publication Year :
- 2012
-
Abstract
- Environmental adaptability is critical for survival of the fungal human pathogen Aspergillus fumigatus in the immunocompromised host lung. We hypothesized that exposure of the fungal pathogen to human serum would lead to significant alterations to the organism's physiology, including metabolic activity and stress response. Shifts in functional pathway and corresponding enzyme reactivity of A. fumigatus upon exposure to the human host may represent much needed prognostic indicators of fungal infection. To address this, we employed a multiplexed activity-based protein profiling (ABPP) approach coupled to quantitative mass spectrometry-based proteomics to measure broad enzyme reactivity of the fungus cultured with and without human serum. ABPP showed a shift from aerobic respiration to ethanol fermentation and utilization over time in the presence of human serum, which was not observed in serum-free culture. Our approach provides direct insight into this pathogen's ability to survive, adapt, and proliferate. Additionally, our multiplexed ABPP approach captured a broad swath of enzyme reactivity and functional pathways and provides a method for rapid assessment of the A. fumigatus response to external stimuli.
- Subjects :
- Biochemistry methods
Culture Media, Serum-Free chemistry
Fungal Proteins chemistry
Gene Expression Regulation, Fungal
Humans
Lung microbiology
Lung Diseases microbiology
Mass Spectrometry methods
Models, Biological
Models, Chemical
Protein Array Analysis
Proteomics methods
Time Factors
Aspergillosis microbiology
Aspergillus fumigatus metabolism
Serum microbiology
Subjects
Details
- Language :
- English
- ISSN :
- 1083-351X
- Volume :
- 287
- Issue :
- 40
- Database :
- MEDLINE
- Journal :
- The Journal of biological chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 22865858
- Full Text :
- https://doi.org/10.1074/jbc.M112.394106