# NeuroViOme: a viral orfeome collection for studies of neurodegenerative disease

**Authors:** Benjamin Weller, Chung-Wen Lin, Simin Rothballer, Michael A. Calderwood, Pascal Falter-Braun, Claudia Falter

PMC · DOI: 10.1007/s13365-025-01303-5 · Journal of Neurovirology · 2026-03-02

## TL;DR

NeuroViOme is a comprehensive collection of viral genes that may help study how viruses contribute to neurodegenerative diseases like Alzheimer's and Parkinson's.

## Contribution

The paper introduces NeuroViOme, the most comprehensive viral ORFeome resource for studying viral-host interactions in neurodegeneration.

## Key findings

- NeuroViOme includes protein-coding sequences from nine viruses linked to neurodegenerative diseases.
- The resource enables systematic studies of viral-host protein interactions in conditions like ALS and MS.
- It provides a foundation for interactome mapping and functional genomics in neurodegeneration research.

## Abstract

Neurodegenerative diseases such as Alzheimer’s and Parkinson’s disease, Amyotrophic Lateral Sclerosis (ALS), and Multiple Sclerosis (MS) pose a global health challenge due to their progressive course and lack of curative therapies. These conditions lead to severe neurological decline, significantly impacting patient independence and quality of life, and ultimately result in lethal outcome. Emerging evidence suggests that viral infections contribute to the onset and progression of these neurological diseases, Leblanc and Vorberg (PLoS Pathog 18:e1010670, 2022), either by directly inducing neurological symptoms or by triggering immune responses resulting in neuropathology. Nevertheless, systematic studies of the direct interplay between viral and host proteins in neurodegeneration remain scarce. A key aspect of viral pathogenesis is direct interaction between viral and host proteins (protein–protein interactions, PPIs), which are essential for viral replication and can disrupt or redirect host cell function Kim et al. (Nat Biotechnol, 2022); Zhou et al. (Res Sq, 2022), potentially contributing to the development of diseases traditionally considered non-communicable. Understanding these molecular mechanisms is crucial for advancing diagnostic and therapeutic strategies in neurodegenerative conditions, particularly ALS and MS. To enable systematic studies of these interactions, we introduce NeuroViOme as ORFeome resource encompassing nearly all protein-coding sequences from nine viruses selected based on their prevalence, neurotropism, and mechanistic or epidemiological links to neurodegenerative processes. NeuroViOme includes ORFs from Enteroviruses (EV-A71, EV-D68, CVB3, Echovirus E30), Herpesviruses (HSV-1, EBV, HHV3/Varicella Zoster), the endogenous retrovirus HERV-K, and Polyomavirus JCPyV. To our knowledge, this represents the most comprehensive viral ORF set assembled for neurodegeneration research to date. The collection builds the foundation for interactome mapping and functional genomics analyses and provides a valuable basis for systematic studies of viral perturbations of host pathways.

The online version contains supplementary material available at 10.1007/s13365-025-01303-5.

## Linked entities

- **Diseases:** Parkinson’s disease (MONDO:0005180), Amyotrophic Lateral Sclerosis (MONDO:0004976), Multiple Sclerosis (MONDO:0005301), ALS (MONDO:0004976), MS (MONDO:0006861)

## Full-text entities

- **Genes:** IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, TLR7 (toll like receptor 7) [NCBI Gene 51284] {aka IMD74, SLEB17, TLR7-like}, TARDBP (TAR DNA binding protein) [NCBI Gene 23435] {aka ALS10, TDP-43}, APP (amyloid beta precursor protein) [NCBI Gene 351] {aka AAA, ABETA, ABPP, AD1, APPI, CTFgamma}, OPTN (optineurin) [NCBI Gene 10133] {aka ALS12, FIP2, GLC1E, HIP7, HYPL, NRP}, MAPT (microtubule associated protein tau) [NCBI Gene 4137] {aka DDPAC, FTD1, FTDP-17, MAPTL, MSTD, MTBT1}, SNCA (synuclein alpha) [NCBI Gene 6622] {aka NACP, PARK1, PARK4, PD1}, APOE (apolipoprotein E) [NCBI Gene 348] {aka AD2, APO-E, ApoE4, LDLCQ5, LPG}
- **Diseases:** proteinopathy (MESH:D057165), aseptic meningitis (MESH:D008582), HHV3 infection (MESH:D007239), encephalitis (MESH:D004660), viral infections (MESH:D014777), demyelinating (MESH:D003711), ALS (MESH:D000690), multifocal leukoencephalopathy (MESH:D007968), neuropathology (MESH:D009422), CNS injury (MESH:D002494), MS (MESH:D009103), dementia (MESH:D003704), neuroinflammation (MESH:D000090862), flaccid myelitis (MESH:C000629404), Cancer (MESH:D009369), AD (MESH:D000544), neurotoxicity (MESH:D020258), Alzheimer's and Parkinson's disease (MESH:D010300), neurodegeneration (MESH:D019636), inflammatory (MESH:D007249), neurological decline (MESH:D009461), autoimmune diseases (MESH:D001327), neurological diseases (MESH:D020271), motor neuron disorders (MESH:D016472)
- **Chemicals:** NeuroViOme (-), glycine (MESH:D005998)
- **Species:** Polyomavirus sp. (species) [taxon 36362], Homo sapiens (human, species) [taxon 9606], human gammaherpesvirus 4 (Epstein Barr virus, no rank) [taxon 10376], Echovirus E30 (no rank) [taxon 41846], JC polyomavirus (no rank) [taxon 10632], Mus musculus (house mouse, species) [taxon 10090], Human T-cell leukemia virus type I (no rank) [taxon 11908], Human endogenous retrovirus K (species) [taxon 45617], Human alphaherpesvirus 1 (Herpes simplex virus type 1, no rank) [taxon 10298], Enterovirus A71 (no rank) [taxon 39054], Human immunodeficiency virus 1 (no rank) [taxon 11676], Coxsackievirus B3 (no rank) [taxon 12072], Human alphaherpesvirus 3 (Varicella-zoster virus, no rank) [taxon 10335], enterovirus D68 (no rank) [taxon 42789]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12953343/full.md

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Source: https://tomesphere.com/paper/PMC12953343