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Updated: Apr 30, 2026

In Vitro Assay of Bacterial Adhesion onto Mammalian Epithelial Cells
Published on: May 16, 2011
Epithelial microvilli establish an electrostatic barrier to microbial adhesion
Kaila M Bennett1, Sharon L Walker2, David D Lo3
1Division of Biomedical Sciences, School of Medicine, University of California-Riverside, Riverside, California, USA Bioengineering Interdepartmental Graduate Program, University of California-Riverside, Riverside, California, USA.
Abstract:
Microvilli are membrane extensions on the apical surface of polarized epithelia, such as intestinal enterocytes and tubule and duct epithelia. One notable exception in mucosal epithelia is M cells, which are specialized for capturing luminal microbial particles; M cells display a unique apical membrane lacking microvilli. Based on studies of M cell uptake under different ionic conditions, we hypothesized that microvilli may augment the mucosal barrier by providing an increased surface charge density from the increased membrane surface and associated glycoproteins. Thus, electrostatic charges may repel microbes from epithelial cells bearing microvilli, while M cells are more susceptible to microbial adhesion. To test the role of microvilli in bacterial adhesion and uptake, we developed polarized intestinal epithelial cells with reduced microvilli ("microvillus-minus," or MVM) but retaining normal tight junctions. When tested for interactions with microbial particles in suspension, MVM cells showed greatly enhanced adhesion and uptake of particles compared to microvillus-positive cells. This preference showed a linear relationship to bacterial surface charge, suggesting that microvilli resist binding of microbes by using electrostatic repulsion. Moreover, this predicts that pathogen modification of electrostatic forces may contribute directly to virulence. Accordingly, the effacement effector protein Tir from enterohemorrhagic Escherichia coli O157:H7 expressed in epithelial cells induced a loss of microvilli with consequent enhanced microbial binding. These results provide a new context for microvillus function in the host-pathogen relationship, based on electrostatic interactions.
Insights
Microvilli on epithelial cells act as a barrier, repelling microbes via electrostatic charge. Reduced microvilli increase microbial adhesion and uptake, highlighting their role in host-pathogen interactions.
Area of Science:
- Cell Biology
- Microbiology
- Immunology
Background:
- Microvilli are apical membrane extensions on polarized epithelial cells.
- M cells, specialized for particle capture, lack microvilli, suggesting a role for microvilli in barrier function.
- Hypothesis: Microvilli increase surface charge density, repelling microbes and augmenting the mucosal barrier.
Purpose of the Study:
- To investigate the role of microvilli in bacterial adhesion and uptake.
- To test if microvilli electrostatic charges repel microbes.
- To understand the host-pathogen relationship in the context of microvilli and electrostatic interactions.
Main Methods:
- Development of polarized intestinal epithelial cells with reduced microvilli (microvillus-minus, MVM cells).
- Assessment of microbial particle adhesion and uptake by MVM cells compared to microvillus-positive cells.
- Expression of enterohemorrhagic Escherichia coli O157:H7 effector protein Tir in epithelial cells.
Main Results:
- MVM cells exhibited significantly enhanced adhesion and uptake of microbial particles compared to control cells.
- Microbial adhesion showed a linear relationship with bacterial surface charge, supporting electrostatic repulsion by microvilli.
- Tir expression induced microvilli loss and increased microbial binding, demonstrating pathogen manipulation of host cell surface.
Conclusions:
- Microvilli function as a crucial component of the mucosal barrier by utilizing electrostatic repulsion to prevent microbial adhesion.
- Reduced microvilli density enhances susceptibility to microbial invasion.
- Pathogen strategies targeting electrostatic interactions, like Tir expression, can contribute to virulence by compromising the microvilli barrier.
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