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Updated: Aug 17, 2025

Dissecting Host-virus Interaction in Lytic Replication of a Model Herpesvirus
Published on: October 7, 2011
Modulation of mitochondria by viral proteins
Reshu Saxena1, Priyanka Sharma2, Sandeep Kumar1
1Immuno-biology Lab, Infection and Immunology Centre, Translational Health Science and Technology Institute, NCR-Biotech Science Cluster, 3rd Milestone, Faridabad-Gurgaon Expressway, Faridabad 121001, Haryana, India.
Viruses hijack mitochondria, crucial cell powerhouses, to control cell death, immunity, and metabolism, enabling infection spread. This review explores viral proteins targeting mitochondria, including in SARS-CoV-2.
Area of Science:
- Cell Biology
- Virology
- Immunology
Background:
- Mitochondria are vital organelles involved in energy production, calcium homeostasis, apoptosis, and immune signaling.
- Viruses exploit mitochondrial functions to evade host defenses and promote infection.
- Mitochondrial dynamics and functions are key targets for viral subversion.
Purpose of the Study:
- To review viral proteins that specifically target mitochondria.
- To elucidate how viruses manipulate mitochondrial functions for replication and persistence.
- To highlight the role of mitochondria in SARS-CoV-2 pathogenesis and host-virus interactions.
Main Methods:
- Literature review of viral-mitochondrial interactions.
- Analysis of viral protein functions targeting mitochondrial dynamics.
- Exploration of host-virus protein interactions at the mitochondrial level.
Main Results:
- Viral proteins alter mitochondrial membrane potential, reactive oxygen species, calcium homeostasis, and bioenergetics.
- Targeting mitochondria allows viruses to control apoptosis, metabolism, and evade immune responses.
- Mitochondrial subversion facilitates viral spread and persistent infections.
Conclusions:
- Understanding viral targeting of mitochondria is crucial for combating viral infections.
- Mitochondrial dysfunction is implicated in the pathogenesis of viruses like SARS-CoV-2.
- Identifying host-virus protein interactions at mitochondria offers therapeutic targets.
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