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Updated: Jun 19, 2026

Immuno-fluorescence Assay of Leptospiral Surface-exposed Proteins
Published on: July 1, 2011
Leptospira interrogans binds to human cell surface receptors including proteoglycans
Deborah D Breiner1, Mark Fahey, Ryan Salvador
1Graduate Program in Molecular Microbiology, Tufts University Sackler School of Graduate Biomedical Sciences, Boston, Massachusetts, USA.
Abstract:
Leptospirosis is a global public health problem, primarily in the tropical developing world. The pathogenic mechanisms of the causative agents, several members of the genus Leptospira, have been underinvestigated. The exception to this trend has been the demonstration of the binding of pathogenic leptospires to the extracellular matrix (ECM) and its components. In this work, interactions of Leptospira interrogans bacteria with mammalian cells, rather than the ECM, were examined. The bacteria bound more efficiently to the cells than to the ECM, and a portion of this cell-binding activity was attributable to attachment to glycosaminoglycan (GAG) chains of proteoglycans (PGs). Chondroitin sulfate B PGs appeared to be the primary targets of L. interrogans attachment, while heparan sulfate PGs were much less important. Inhibition of GAG/PG-mediated attachment resulted in partial inhibition of bacterial attachment, suggesting that additional receptors for L. interrogans await identification. GAG binding may participate in the pathogenesis of leptospirosis within the host animal. In addition, because GAGs are expressed on the luminal aspects of epithelial cells in the proximal tubules of the kidneys, this activity may play a role in targeting the bacteria to this critical site. Because GAGs are shed in the urine, GAG binding may also be important for transmission to new hosts through the environment.
Insights
Leptospira interrogans bacteria bind efficiently to mammalian cells, particularly to chondroitin sulfate B proteoglycans. This glycosaminoglycan binding may be crucial for leptospirosis pathogenesis and transmission.
Area of Science:
- Microbiology
- Pathogenesis
- Infectious Diseases
Background:
- Leptospirosis is a significant global health issue, especially in tropical regions.
- The pathogenic mechanisms of Leptospira, the bacteria causing leptospirosis, are not fully understood.
- Previous research highlighted Leptospira's interaction with the extracellular matrix (ECM).
Purpose of the Study:
- To investigate the interactions between Leptospira interrogans and mammalian cells.
- To identify specific bacterial binding targets on host cells.
- To explore the role of these interactions in disease development and transmission.
Main Methods:
- Examined the binding of Leptospira interrogans to mammalian cells and ECM components.
- Investigated the role of glycosaminoglycans (GAGs) and proteoglycans (PGs) in bacterial attachment.
- Assessed the impact of inhibiting GAG/PG-mediated attachment on bacterial binding.
Main Results:
- Leptospira interrogans exhibited higher binding efficiency to mammalian cells compared to the ECM.
- A significant portion of cell-binding activity was mediated by attachment to GAG chains of PGs.
- Chondroitin sulfate B PGs were identified as primary attachment targets, while heparan sulfate PGs were less important.
- Inhibiting GAG/PG attachment partially reduced overall bacterial attachment, indicating other receptors exist.
Conclusions:
- Leptospira interrogans binding to mammalian cell GAGs, especially chondroitin sulfate B PGs, is a key interaction.
- This GAG binding may contribute to leptospirosis pathogenesis by targeting bacteria to host tissues like the kidneys.
- GAG binding could also facilitate environmental transmission of Leptospira through urine.
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