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Updated: Feb 1, 2026

Detection of Functional Matrix Metalloproteinases by Zymography
Published on: November 8, 2010
Enhanced Systemic Response of Matrix Metalloproteinases and Their Regulators in Campylobacter and Salmonella Patients
Anna Nilsson1, Taina Tervahartiala2, David Lennebratt3
1Department of Medical Sciences, Clinical Microbiology, Uppsala University, Dag Hammarskjölds väg 38, 75237 Uppsala, Sweden. anna.nilsson@medsci.uu.se.
Abstract:
Campylobacters are major enteropathogens worldwide with a substantial financial burden. Matrix metalloproteinases (MMPs) are proteolytic metalloendopeptidases with ability to modify immune response and shown to be upregulated in patients with several tissue destructive diseases, including infections. We measured here serum concentrations of MMP-8 and MMP-9 together with their regulators myeloperoxidase (MPO), human neutrophil elastase (HNE), and tissue inhibitor of metalloproteinases (TIMP)-1 in 80 Campylobacter and 25 Salmonella patients as well as in 27 healthy controls. Paired serum samples were available for 73 and 23 patients, respectively. When the initial serum samples were compared to those from controls, both Campylobacter and Salmonella patients showed elevated concentrations of all biomarkers tested (p ≤ 0.037). In the follow-up samples, collected about 25 days afterwards, MMP-8 levels of Campylobacter patients had already turned to normal but all the other biomarkers still showed elevated, although from the initial levels significantly dropped, levels. For the follow-up samples of Salmonella patients, only MMP-9 and MPO levels were at a significantly higher level than in controls. It remains to be studied if the systematically enhanced neutrophil-derived proteolytic and oxidative stress, induced by Campylobacter infection as shown here and persisting for several weeks, is important for the development of late sequelae.
Insights
Campylobacter and Salmonella infections elevate key immune biomarkers like MMP-8 and MMP-9. While levels normalize for Campylobacter patients within weeks, persistent inflammation may link to long-term complications.
Area of Science:
- Immunology
- Infectious Diseases
- Biochemistry
Background:
- Campylobacters are significant global enteropathogens causing considerable financial strain.
- Matrix metalloproteinases (MMPs) modulate immune responses and are elevated in infectious and tissue-destructive diseases.
- Neutrophil-derived proteins, including MMPs, myeloperoxidase (MPO), and human neutrophil elastase (HNE), play roles in infection and inflammation.
Purpose of the Study:
- To investigate serum concentrations of MMP-8, MMP-9, MPO, HNE, and tissue inhibitor of metalloproteinases (TIMP)-1 in patients with Campylobacter and Salmonella infections.
- To compare these biomarker levels between infected patients and healthy controls.
- To assess the temporal changes in these biomarkers during the course of infection.
Main Methods:
- Serum samples were collected from 80 Campylobacter patients, 25 Salmonella patients, and 27 healthy controls.
- Initial and follow-up serum samples (approx. 25 days later) were analyzed for MMP-8, MMP-9, MPO, HNE, and TIMP-1 concentrations.
- Statistical analysis was performed to compare biomarker levels between groups and over time.
Main Results:
- Both Campylobacter and Salmonella patients exhibited elevated levels of all tested biomarkers compared to controls in initial samples (p ≤ 0.037).
- In follow-up samples, Campylobacter patients showed normalized MMP-8 levels, but other biomarkers remained elevated (though decreased from initial levels).
- Salmonella patients' follow-up samples indicated significantly higher MMP-9 and MPO levels compared to controls.
Conclusions:
- Campylobacter infection induces a sustained, weeks-long elevation in neutrophil-derived proteolytic and oxidative stress markers.
- The persistent inflammatory markers following Campylobacter infection warrant further investigation for potential links to late sequelae.
- MMP-9 and MPO elevations persist longer in Salmonella infections compared to Campylobacter infections.
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