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Updated: Apr 18, 2026

Dissecting Host-virus Interaction in Lytic Replication of a Model Herpesvirus
Published on: October 7, 2011
Viral-host interactions mediated by the mTOR signaling pathway
Zizhen Ming1,2, Bing Su1,2,3,4, Qiming Liang1,2
1Center for Immune-Related Diseases at Shanghai Institute of Immunology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200025, China.
Viruses hijack the mechanistic target of rapamycin (mTOR) pathway to fuel replication by manipulating host metabolism and autophagy. Targeting mTOR offers a promising antiviral strategy by disrupting these virus-host interactions.
Area of Science:
- Cellular Biology
- Virology
- Biochemistry
Background:
- The mechanistic target of rapamycin (mTOR) is a key kinase regulating cellular processes like metabolism and survival.
- Viruses depend on host cell machinery, making the mTOR pathway crucial for viral propagation.
- mTOR exists in two complexes, mTORC1 and mTORC2, integrating cellular signals.
Purpose of the Study:
- To review how viruses manipulate mTOR signaling for replication.
- To explore mTOR's role in antiviral immunity.
- To discuss mTOR-targeted antiviral strategies.
Main Methods:
- Systematic review of literature on mTOR signaling and viral interactions.
- Analysis of viral strategies to modulate mTORC1 and mTORC2.
- Examination of preclinical and clinical data on mTOR inhibitors.
Main Results:
- Viruses activate host metabolism and inhibit autophagy via mTOR to support replication.
- Viruses dynamically tune mTORC1 and mTORC2 activity for different replication stages.
- mTOR plays a significant role in antiviral immune responses.
Conclusions:
- mTOR is a critical regulator of virus-host interactions, essential for viral life cycles.
- Targeting mTOR presents a viable strategy for developing novel antiviral therapies.
- Understanding mTOR modulation provides a framework for antiviral intervention development.
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