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Updated: Jun 27, 2026

Enriching Subcellular Proteins in Leptospira Using a Triton X-114-Based Fractionation Approach
Published on: August 8, 2025
[Adhering effect of Leptospira interrongan to major extracellular matrix molecules]
Hao Zhang1, Ai-hua Sun, Jie Yan
1Department of Microbiology and Parasitology, College of Medicine, Zhejiang University, Hangzhou 310058, China.
Objective:
To determine the adhering ability of Leptospira interrogans to extracellular matrix molecules (ECM) of host cells and its diversity.
Methods:
The infection models of L. interrogans serogroup Icterohaemorrhagiae serovar lai strain 56601 to J774A.1, L929 and Vero cells were established. Fontana silver impregnation method was applied to demonstrate the adhering effect of microbes to extracellular matrix (ECM) of the cells. ELISA methods were established to detect the adhering effects of L. interrogans to ECM molecules laminin (LN), fibronectin (FN), decorin (DEN) and collagen1, 2, 4 (COL1, 2, 4). A competitive inhibition test was performed to verify the results.
Result:
L. interrogans strain 56601 adhered the ECMs of L929, J774A.1 and Vero cells with its one or two sites. L. interrogans strain 56601 adhered all six ECM molecules; the adhering effects to COL1, LN, COL4 were relatively stronger. The adhering effects were markedly decreased after the microbes were pre-incubated with corresponding ECM molecules.
Conclusion:
L. interrogans adheres to host cells through ECM molecules; LN, FN, DEN, COL1, COL2 and COL4 are the receptor molecules with different adhesion intensity.
Insights
Leptospira interrogans bacteria bind to host cell extracellular matrix (ECM) molecules. This study identifies specific ECM components like collagen and laminin as key binding sites for L. interrogans adhesion.
Area of Science:
- Microbiology
- Cell Biology
- Infectious Diseases
Background:
- Leptospira interrogans is a pathogenic bacterium responsible for leptospirosis.
- Understanding bacterial adhesion mechanisms is crucial for developing effective treatments.
Purpose of the Study:
- To investigate the adhesion capabilities of L. interrogans to host cell extracellular matrix (ECM) components.
- To identify the specific ECM molecules involved in L. interrogans attachment.
Main Methods:
- Established infection models using L. interrogans with J774A.1, L929, and Vero cells.
- Employed Fontana silver impregnation and ELISA to assess bacterial adhesion to ECM molecules (laminin, fibronectin, decorin, collagen types 1, 2, and 4).
- Utilized competitive inhibition assays to validate adhesion findings.
Main Results:
- L. interrogans strain 56601 demonstrated adherence to the ECM of all tested cell lines.
- The bacterium bound to all six tested ECM molecules, with stronger adhesion observed for collagen 1, laminin, and collagen 4.
- Pre-incubation with ECM molecules significantly reduced bacterial adhesion.
Conclusions:
- Leptospira interrogans utilizes host cell ECM molecules for adhesion.
- Laminin, fibronectin, decorin, collagen 1, collagen 2, and collagen 4 act as receptors for L. interrogans, with varying affinities.
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