Host control and regulation of human anellovirus persistence

Anelloviruses are the most abundant and diverse eukaryotic viruses known to infect humans and can persist throughout our lifetimes. Despite their ubiquity, the host factors governing their physiologic distribution and abundance remain poorly understood. Here, we construct a viral pangenome of 2,023 strains to quantify anellovirus DNA in >1.1 million participants spanning three genetic biobanks. Genome-wide association studies identify 121 loci linked to viral persistence, predominantly via immune regulation by NF-kB signaling. Further, we associate variable anellovirus detection with conditions characterized by immune dysfunction, including lymphoid malignancies. By screening 3.2 petabases of human single-cell sequencing data, we identify myeloid progenitors in the bone marrow as a prominent site of anellovirus transcription in vivo. Finally, Perturb-seq of anellovirus proteins reveals that anellovirus ORF2, particularly from Alphatorquevirus, attenuates TNF-a-induced NF-kB signaling, connecting host genetic variation, cellular context, and viral immunomodulation to characterize the persistence of the eukaryotic human virome's most abundant component.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-11-09
DOI
https://doi.org/10.64898/2026.11.05.764726
Primary Topic
Viral-associated cancers and disorders
Type
preprint
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preprint

Host control and regulation of human anellovirus persistence

Thahmina A. Ali, Sherry S. Y. Nyeo, Konstantin Helmsauer, Eli Metzner et al.
bioRxiv (Cold Spring Harbor Laboratory)
Viral-associated cancers and disorders
preprint

Host control and regulation of human anellovirus persistence

Thahmina A. Ali, Sherry S. Y. Nyeo, Konstantin Helmsauer, Eli Metzner, Jun Hao Neo, Kushal K. Dey, Ryan S. Dhindsa, Caleb A. Lareau, Rico Chandra Ardy, Austin Varela, Rayan Chikhi, Jacob C. Ulirsch, Jacob C. Gutierrez, Christopher Cole Honeycutt, Thomas M. Norman, Petko P. Fiziev, Ann Le, Allison J. Vela, Laura C. Kida
preprint en

Abstract

Anelloviruses are the most abundant and diverse eukaryotic viruses known to infect humans and can persist throughout our lifetimes. Despite their ubiquity, the host factors governing their physiologic distribution and abundance remain poorly understood. Here, we construct a viral pangenome of 2,023 strains to quantify anellovirus DNA in >1.1 million participants spanning three genetic biobanks. Genome-wide association studies identify 121 loci linked to viral persistence, predominantly via immune regulation by NF-kB signaling. Further, we associate variable anellovirus detection with conditions characterized by immune dysfunction, including lymphoid malignancies. By screening 3.2 petabases of human single-cell sequencing data, we identify myeloid progenitors in the bone marrow as a prominent site of anellovirus transcription in vivo. Finally, Perturb-seq of anellovirus proteins reveals that anellovirus ORF2, particularly from Alphatorquevirus, attenuates TNF-a-induced NF-kB signaling, connecting host genetic variation, cellular context, and viral immunomodulation to characterize the persistence of the eukaryotic human virome's most abundant component.

bioRxiv (Cold Spring Harbor Laboratory)
Memorial Sloan Kettering Cancer Center (US), Institut Pasteur (FR), Baylor College of Medicine (US), Illumina (United Kingdom) (GB), Illumina (Singapore) (SG)
Viral-associated cancers and disorders
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