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Published on: June 21, 2021
Oxidative modification of proteins in pediatric cystic fibrosis with bacterial infections
Izabela Sadowska-Bartosz1, Sabina Galiniak1, Grzegorz Bartosz2
1Department of Biochemistry and Cell Biology, University of Rzeszów, Zelwerowicza 4, 35-601 Rzeszów, Poland.
Insights
Cystic fibrosis (CF) patients with chronic lung infections show increased oxidative stress markers. Glycophores and protein carbonyls are useful indicators of oxidative damage in CF patients.
Area of Science:
- Biochemistry
- Pulmonology
- Medical Research
Background:
- Chronic lung infections by Pseudomonas aeruginosa and Staphylococcus aureus are common in cystic fibrosis (CF) patients.
- These infections induce significant oxidative stress in CF patients.
- Understanding oxidative stress markers is crucial for managing CF.
Purpose of the Study:
- To compare markers of plasma protein oxidative damage and glycoxidation in CF patients with chronic P. aeruginosa and S. aureus infections.
- To assess erythrocyte antioxidant enzyme activities in these patients.
- To investigate nitric oxide concentration in exhaled air of CF patients.
Main Methods:
- Comparison of plasma protein oxidative damage and glycoxidation markers (glycophores, carbonyl groups, kynurenine).
- Measurement of erythrocyte glutathione S-transferase activity.
- Quantification of nitric oxide in exhaled air.
Main Results:
- Elevated glycophore and protein carbonyl levels were observed in CF patients infected with P. aeruginosa and S. aureus compared to controls.
- Increased glutathione S-transferase activity was noted in both infection groups.
- Kynurenine levels were elevated specifically in S. aureus infected CF patients.
Conclusions:
- These findings confirm the presence of oxidative stress in CF patients with chronic lung infections.
- Glycophores and protein carbonyls serve as valuable markers for oxidative modifications of plasma proteins in CF.
- Further research into antioxidant strategies for CF management is warranted.
Abstract:
Pseudomonas aeruginosa and Staphylococcus aureus cause chronic lung infection in cystic fibrosis (CF) patients, inducing chronic oxidative stress. Several markers of plasma protein oxidative damage and glycoxidation and activities of erythrocyte antioxidant enzymes have been compared in stable CF patients chronically infected with Pseudomonas aeruginosa (n = 12) and Staphylococcus aureus (n = 10) in relation to healthy subjects (n = 11). Concentration of nitric oxide was also measured in the exhaled air from the lower respiratory tract of patients with CF. Elevated glycophore (4.22 ± 0.91 and 4.19 ± 1.04 versus control 3.18 ± 0.53 fluorescence units (FU)/mg protein; P < 0.05) and carbonyl group levels (1.9 ± 0.64, 1.87 ± 0.45 versus control 0.94 ± 0.19 nmol/mg protein; P < 0.05) as well as increased glutathione S-transferase activity (2.51 ± 0.88 and 2.57 ± 0.79 U/g Hb versus 0.77 ± 0.16 U/g Hb; P < 0.05) were noted in Pseudomonas aeruginosa and Staphylococcus aureus infected CF. Kynurenine level (4.91 ± 1.22 versus 3.89 ± 0.54 FU/mg protein; P < 0.05) was elevated only in Staphylococcus aureus infected CF. These results confirm oxidative stress in CF and demonstrate the usefulness of the glycophore level and protein carbonyl groups as markers of oxidative modifications of plasma proteins in this disease.
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