# Metabolic hijackers: how viral proteins redefine host cell landscapes

**Authors:** Adam Hafner, Rebekah L. Mokry, John G. Purdy, Christiane E. Wobus

PMC · DOI: 10.1128/jvi.00556-25 · Journal of Virology · 2026-01-09

## TL;DR

This review explores how viruses alter host cell metabolism through specific viral proteins to support their replication and survival.

## Contribution

The paper identifies key metabolic pathways targeted by viruses and highlights gaps in understanding the mechanisms of viral metabolic reprogramming.

## Key findings

- Viruses manipulate glycolysis, glutaminolysis, and lipid metabolism to secure resources for replication.
- Specific viral proteins are responsible for reshaping the host cell's metabolic environment.
- Understanding these mechanisms could lead to new therapeutic strategies against viral infections.

## Abstract

Viruses are metabolic engineers of host cells. As obligate intracellular pathogens, they rely on host cell metabolism for efficient viral replication. The manipulation of host metabolic processes is a strategy shared among diverse virus families to secure the necessary resources for replicating new genomes, building more virus particles, and supporting cell growth and proliferation. Key metabolic pathways targeted by viruses for disruption and manipulation are glycolysis, glutaminolysis, and lipid metabolism. However, the mechanisms behind virus-induced metabolic reprogramming and the viral proteins mediating it remain poorly understood. This review explores how specific viral proteins reshape the metabolic milieu of host cells during viral infections. We also highlight common themes and outline gaps in knowledge to stimulate further investigations into how viral proteins manipulate host metabolism. Such mechanistic insights will deepen our understanding of virus-host interactions and may reveal novel therapeutic targets.

## Full-text entities

- **Diseases:** viral infections (MESH:D014777)
- **Chemicals:** lipid (MESH:D008055)

## Full text

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## Figures

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## References

81 references — full list in the complete paper: https://tomesphere.com/paper/PMC12911867/full.md

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Source: https://tomesphere.com/paper/PMC12911867