# Virus infection and vesicle trafficking

**Authors:** Guo-Xiu Cao, Fan-Xin Liu, Chun-Chun Meng, Chan Ding, Jun Dai, Xu-Sheng Qiu

PMC · DOI: 10.3389/fimmu.2025.1682139 · Frontiers in Immunology · 2025-10-09

## TL;DR

This review explores how viruses use the cell's vesicle trafficking system during infection and how targeting these pathways could lead to new antiviral treatments.

## Contribution

The paper systematically examines how viruses manipulate host vesicle trafficking at different infection stages and evaluates vesicle-targeted antiviral strategies.

## Key findings

- Viruses exploit host vesicle trafficking proteins to optimize entry and immune evasion.
- Vesicle trafficking is involved in multiple stages of the viral replication cycle.
- Targeting vesicle transport nodes shows promise as an antiviral therapeutic strategy.

## Abstract

Vesicle trafficking mechanisms play indispensable roles throughout the viral replication cycle, though their stage-specific regulatory mechanisms during infection require further elucidation. Notably, the latest research reveals that diverse viruses strategically exploit host vesicle trafficking proteins to orchestrate critical infection phases, including receptor-mediated endocytosis initiation, viral attachment/membrane fusion, intracellular component transport, genome replication complex reorganization, and viral assembly/budding. By commandeering these trafficking pathways, viruses not only optimize cellular entry efficiency and immune evasion capabilities but also establish dynamic organelle microenvironments conducive to genome replication. Consequently, therapeutic strategies targeting vesicular transport nodes—through functional inhibition of trafficking proteins or disruption of vesicle homeostasis—have emerged as promising antiviral approaches with clinical translation potential. This review systematically examines viral phase-dependent mechanisms of host vesicular networks, elucidates infection optimization through transport pathway subversion, and evaluates current efforts in developing vesicle-targeted antivirals, thereby providing conceptual frameworks for novel therapeutic design.

## Full-text entities

- **Diseases:** infection (MESH:D007239)

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12548552/full.md

## References

412 references — full list in the complete paper: https://tomesphere.com/paper/PMC12548552/full.md

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Source: https://tomesphere.com/paper/PMC12548552