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Updated: Nov 17, 2025

Invasion of Human Cells by a Bacterial Pathogen
Published on: March 21, 2011
Manipulation of Focal Adhesion Signaling by Pathogenic Microbes
Korinn N Murphy1,2, Amanda J Brinkworth2
1School of Molecular Biosciences, Washington State University, Pullman, WA 99164, USA.
Abstract:
Focal adhesions (FAs) serve as dynamic signaling hubs within the cell. They connect intracellular actin to the extracellular matrix (ECM) and respond to environmental cues. In doing so, these structures facilitate important processes such as cell-ECM adhesion and migration. Pathogenic microbes often modify the host cell actin cytoskeleton in their pursuit of an ideal replicative niche or during invasion to facilitate uptake. As actin-interfacing structures, FA dynamics are also intimately tied to actin cytoskeletal organization. Indeed, exploitation of FAs is another avenue by which pathogenic microbes ensure their uptake, survival and dissemination. This is often achieved through the secretion of effector proteins which target specific protein components within the FA. Molecular mimicry of the leucine-aspartic acid (LD) motif or vinculin-binding domains (VBDs) commonly found within FA proteins is a common microbial strategy. Other effectors may induce post-translational modifications to FA proteins through the regulation of phosphorylation sites or proteolytic cleavage. In this review, we present an overview of the regulatory mechanisms governing host cell FAs, and provide examples of how pathogenic microbes have evolved to co-opt them to their own advantage. Recent technological advances pose exciting opportunities for delving deeper into the mechanistic details by which pathogenic microbes modify FAs.
Insights
Pathogenic microbes exploit host cell focal adhesions (FAs) to invade and survive. This review details how microbes manipulate FAs via effector proteins, impacting cell adhesion and migration.
Area of Science:
- Cell Biology
- Microbiology
- Biochemistry
Background:
- Focal adhesions (FAs) are crucial signaling hubs connecting the cell's actin cytoskeleton to the extracellular matrix (ECM).
- FAs regulate essential cellular processes like adhesion and migration, and are vital for cell-ECM interactions.
- Pathogenic microbes often target the host cell actin cytoskeleton to facilitate invasion, replication, and dissemination.
Purpose of the Study:
- To review the regulatory mechanisms of host cell focal adhesions.
- To provide examples of how pathogenic microbes exploit focal adhesions for their own benefit.
- To highlight recent technological advances for studying microbe-FA interactions.
Main Methods:
- This review synthesizes existing literature on focal adhesion regulation and microbial manipulation.
- It examines effector proteins secreted by pathogens that target focal adhesion components.
- The review discusses molecular mimicry (e.g., LD motifs, VBDs) and post-translational modifications (phosphorylation, cleavage) as microbial strategies.
Main Results:
- Pathogenic microbes have evolved sophisticated strategies to hijack host cell focal adhesions.
- Microbial effectors mimic FA protein motifs or induce post-translational modifications to disrupt FA dynamics.
- Exploitation of FAs aids microbial invasion, survival, and dissemination.
Conclusions:
- Focal adhesions are key targets for pathogenic microbes seeking to manipulate host cell functions.
- Understanding these interactions is critical for developing strategies against microbial pathogenesis.
- Emerging technologies offer new avenues to explore the intricate mechanisms of microbe-FA co-option.
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