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Host-cell dependent epigenetic profiles associated with survival outcomes in T. gondii infection.

Overview

Authors: Loic Ciampossin1, Arzu Ulu2, Todd Lenz1, Zehao Li1, Steven Abel1, Sandeep Srivastava2, Michael White2, Emma Wilson2, Karine G Le Roch1
  1. Department of Molecular, Cell and Systems Biology, University of California Riverside, 900 University Avenue, Riverside, CA 92521 USA
  2. Division of Biomedical Sciences, University of California Riverside, 900 University Avenue, Riverside, CA 92521 USA
Institutions: University of California, Riverside (United States)
Journal: Epigenetics & chromatin, volume 19, issue 1, article 27
Dates: received 23 December 2025; accepted 14 April 2026; published online 5 May 2026
Type: Research article · Language: English
License: CC BY
Identifiers: DOI 10.1186/s13072-026-00678-x · PMID 42087241 · PMCID PMC13317167 · OpenAlex W7160324593
Open access: gold, a free copy (OpenAlex)
Status: data only
Categories: genetics / omics (modality), human (organism), mouse (organism), other condition (population)
MeSH: Epigenesis, Genetic*, Host-Parasite Interactions*, Toxoplasma*, Toxoplasmosis*, Animals, Astrocytes, Fibroblasts, Histones, Humans, Male, Mice, Transcriptome (* major topic)
Topic: Toxoplasma gondii Research Studies (Parasitology, Immunology and Microbiology), according to OpenAlex
Funding: University of California, Riverside (NIFA-Hatch-225935); NIAID NIH HHS (R21 AI142506, R01 AI158417)
Citations: not cited yet (Europe PMC); 45 references in the paper

Abstract

Toxoplasmosis is a widespread parasitic disease affecting roughly one-third of the global population. In immunocompromised individuals or during pregnancy, infection can result in severe complications. Following primary infection, Toxoplasma gondii forms dormant bradyzoite cysts in tissues such as the brain and eyes. These cysts can rupture, particularly in immunocompromised hosts, releasing active parasites and triggering recrudescence. Efforts to experimentally induce and study bradyzoite cyst recrudescence have been hindered by the limited capacity of cell culture adapted strains to form tissue cysts in vivo. T. gondii employs diverse strategies to persist within host cells, including manipulation of host metabolism and immune responses, and these strategies may vary by host cell type. Here, we profiled epigenomic and transcriptomic features associated with differential parasite survival in distinct cell types. Using an ex vivo model of the Type II ME49 strain unadapted to fibroblast culture, we compared parasite survival and epigenetic profiles in neonatal mouse astrocytes (AST) and human foreskin fibroblasts (HFF). Comparative analyses revealed marked divergence in parasite population dynamics, accompanied by reduced H3K4me3 enrichment at promoter regions in parasites grown in HFF. This epigenetic shift correlated with transcriptomic changes in genes linked to cell cycle progression, growth, and development, including a subset of AP2 transcription factors, underscoring the influence of host cell type on parasite biology.

Supplementary Information: The online version contains supplementary material available at 10.1186/s13072-026-00678-x.

Reproduced under the paper's license (CC BY), from the paper cited above.

Code

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Data

Datasets cited

Data availability

All data are present in the main text and the supplementary materials. All biological materials and data are available from the authors upon request. ChIP-seq and RNAseq data are available in NCBI SRA https://www.ncbi.nlm.nih.gov/bioproject/PRJNA1433593 (PRJNA1433593).

Reproduced under the paper's license (CC BY), from the paper cited above.

Versions

The history of this record: each version stored by the harvester or made by a correction of its authors or of the maintainers of its code, and what changed in its facts. The texts of the paper (its abstract, its availability statements) are not part of it; versions that changed only those are not listed.

Version 1, 28 September 2026: the first record

Recorded: type, language, journal, volume, issue, pages, dates, 9 authors, 12 MeSH terms, 2 funders, 43 references.

Cite

This paper

Ciampossin, L., Ulu, A., Lenz, T., Li, Z., Abel, S., Srivastava, S., White, M., Wilson, E., & G Le Roch, K. (2026). Host-cell dependent epigenetic profiles associated with survival outcomes in T. gondii infection. Epigenetics & chromatin, 19(1), 27. https://doi.org/10.1186/s13072-026-00678-x

BibTeX

@article{ciampossin2026host,
author = {Ciampossin, Loic and Ulu, Arzu and Lenz, Todd and Li, Zehao and Abel, Steven and Srivastava, Sandeep and White, Michael and Wilson, Emma and G Le Roch, Karine},
title = {{Host-cell dependent epigenetic profiles associated with survival outcomes in T. gondii infection}},
journal = {Epigenetics \& chromatin},
year = {2026},
month = may,
volume = {19},
number = {1},
pages = {27},
publisher = {BMC},
issn = {1756-8935},
doi = {10.1186/s13072-026-00678-x},
url = {https://doi.org/10.1186/s13072-026-00678-x},
pmid = {42087241},
pmcid = {PMC13317167}
}

RIS

TY - JOUR
AU - Ciampossin, Loic
AU - Ulu, Arzu
AU - Lenz, Todd
AU - Li, Zehao
AU - Abel, Steven
AU - Srivastava, Sandeep
AU - White, Michael
AU - Wilson, Emma
AU - G Le Roch, Karine
TI - Host-cell dependent epigenetic profiles associated with survival outcomes in T. gondii infection
T2 - Epigenetics & chromatin
J2 - Epigenetics Chromatin
PY - 2026
DA - 2026/05/05
VL - 19
IS - 1
SP - 27
SN - 1756-8935
PB - BMC
DO - 10.1186/s13072-026-00678-x
UR - https://doi.org/10.1186/s13072-026-00678-x
LA - en
ER -

CSL-JSON

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