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Published on: February 10, 2014
Virus-associated disruption of mucosal epithelial tight junctions and its role in viral transmission and spread
1Department of Medicine, School of Medicine, University of California-San Francisco, San Francisco, CA, USA.
Abstract:
Oropharyngeal, airway, intestinal, and genital mucosal epithelia are the main portals of entry for the majority of human pathogenic viruses. To initiate systemic infection, viruses must first be transmitted across the mucosal epithelium and then spread across the body. However, mucosal epithelia have well-developed tight junctions, which have a strong barrier function that plays a critical role in preventing the spread and dissemination of viral pathogens. Viruses can overcome these barriers by disrupting the tight junctions of mucosal epithelia, which facilitate paracellular viral penetration and initiate systemic disease. Disruption of tight and adherens junctions may also release the sequestered viral receptors within the junctional areas, and liberation of hidden receptors may facilitate viral infection of mucosal epithelia. This review focuses on possible molecular mechanisms of virus-associated disruption of mucosal epithelial junctions and its role in transmucosal viral transmission and spread.
Insights
Viruses breach mucosal barriers by disrupting epithelial tight junctions, enabling viral entry and systemic spread. Understanding these mechanisms is key to preventing viral transmission.
Area of Science:
- Virology
- Cell Biology
- Immunology
Background:
- Mucosal epithelia serve as primary entry points for many viral pathogens.
- Epithelial tight junctions form a robust barrier crucial for preventing pathogen dissemination.
- Viruses must overcome this barrier to initiate systemic infections.
Purpose of the Study:
- To review the molecular mechanisms viruses employ to disrupt mucosal epithelial junctions.
- To explore the role of junctional disruption in transmucosal viral transmission and spread.
Main Methods:
- Literature review of viral pathogenesis and epithelial barrier function.
- Analysis of molecular pathways involved in viral disruption of tight and adherens junctions.
Main Results:
- Viruses disrupt tight junctions, facilitating paracellular viral penetration.
- Junctional disruption can expose or release viral receptors, enhancing epithelial infection.
- Mechanisms involve direct viral protein interactions or host cell signaling modulation.
Conclusions:
- Virus-induced disruption of mucosal epithelial junctions is a critical step in initiating systemic infection.
- Targeting these viral strategies could offer new avenues for antiviral therapies.
- Further research into specific molecular interactions is warranted to fully elucidate viral transmucosal spread.
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