# Apolipoprotein E selectively supports gammaherpesvirus replication in macrophages

**Authors:** Damon L. Schmalzriedt, Carlie A. Aurubin, Cade R. Rahlf, Matthew A. Brown, Jordan M. Bobek, Philip T. Lange, Xander G. Bradeen, Daisy Sahoo, Vera L. Tarakanova

PMC · DOI: 10.1128/jvi.00480-25 · Journal of Virology · 2025-05-29

## TL;DR

Apolipoprotein E helps gammaherpesviruses replicate in macrophages during their active life cycle, but does not affect their latent state.

## Contribution

ApoE's role in gammaherpesvirus replication is identified as specific to the lytic phase and independent of its usual lipid-regulating functions.

## Key findings

- ApoE expression increases in MHV68-infected macrophages via type-I interferon signaling.
- ApoE supports lytic replication of gammaherpesviruses in macrophages.
- ApoE does not influence the establishment of viral latency in vivo.

## Abstract

Gammaherpesviruses establish lifelong infections in over 90% of adults worldwide and contribute to the development of several cancers. Endogenous lipid synthesis pathways support lytic and latent life cycles of several gammaherpesviruses. However, the role of circulating lipoproteins and the corresponding apolipoproteins in gammaherpesvirus infection remains unknown. Apolipoprotein E (ApoE) is a protein that associates with lipoproteins in circulation and supports bidirectional lipid transport to maintain lipid homeostasis. Interestingly, ApoE differentially affects several virus families, but its role in gammaherpesvirus infection has not been evaluated. In this study, we demonstrate that ApoE expression was increased in murine gammaherpesvirus 68 (MHV68)-infected macrophages in a type-I interferon (IFN)-dependent manner. Intriguingly, ApoE expression was usurped to support MHV68 lytic replication and expression of lytic viral genes. The proviral effects of ApoE in macrophages were independent of the conventional functions of ApoE in the regulation of endogenous lipid synthesis and type I IFN signaling. Finally, the proviral effects of ApoE were limited to the lytic life cycle, as the establishment of MHV68 latency in macrophages was not altered by the ApoE genotype of chronically infected mice. Thus, our study defines a viral life cycle-specific proviral role of ApoE in gammaherpesvirus infection.

ApoE is an apolipoprotein that mediates lipid transport and exchange between tissues and the circulation. ApoE differentially affects several virus families, but its role in gammaherpesvirus infection remains unknown. Here, we show that ApoE supported lytic gammaherpesvirus replication in primary macrophages and that infected macrophages increased expression of ApoE in an interferon-dependent manner. However, ApoE expression did not affect viral latency in vivo, implying a novel viral life cycle-specific proviral role for ApoE in gammaherpesvirus infection.

## Linked entities

- **Genes:** APOE (apolipoprotein E) [NCBI Gene 348]
- **Proteins:** APOE (apolipoprotein E)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** APOE (apolipoprotein E) [NCBI Gene 348] {aka AD2, APO-E, ApoE4, LDLCQ5, LPG}, IFNA1 (interferon alpha 1) [NCBI Gene 3439] {aka IFL, IFN, IFN-ALPHA, IFN-alphaD, IFNA13, IFNA@}
- **Diseases:** cancers (MESH:D009369), gammaherpesvirus infection (MESH:D007239)
- **Chemicals:** lipid (MESH:D008055)
- **Species:** Murid gammaherpesvirus 4 (Murine herpesvirus 68, no rank) [taxon 33708], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

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## References

75 references — full list in the complete paper: https://tomesphere.com/paper/PMC12172433/full.md

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Source: https://tomesphere.com/paper/PMC12172433