Evidence map›Paper›PMID 39141344›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2024

Microsporidian EnP1 alters host cell H2B monoubiquitination and prevents ferroptosis facilitating microsporidia survival.

Jingyu Guan, Liyuan Tang, Yongliang Wang, Ming Fu, Tian Xia, Kai Zheng, Musa Makongoro Sabi, Hua Cong, Juncheng Wang, Chunxue Zhou and 4 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Serpin 4/5 ofMicroorganisms · 2026
    Article
  5. Article
  6. Article
  7. Article
  8. Microsporidian EnP1 alters host cell H2B monoubiquitination and prevents ferroptosis facilitating microsporidia survival.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Jingyu GuanDepartment of Pathogenic Biology, School of Basic Medical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, Shandong 250012, China.ORCID 0000-0001-9620-1656
Liyuan TangDepartment of Pathogenic Biology, School of Basic Medical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, Shandong 250012, China.ORCID 0009-0009-6644-5356
Yongliang WangDepartment of Pathogenic Biology, School of Basic Medical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, Shandong 250012, China.
Ming FuDepartment of Pathogenic Biology, School of Basic Medical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, Shandong 250012, China.ORCID 0000-0002-0757-1776
Tian XiaDepartment of Pathogenic Biology, School of Basic Medical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, Shandong 250012, China.
Kai ZhengDepartment of Pathogenic Biology, School of Basic Medical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, Shandong 250012, China.
Musa Makongoro SabiDepartment of Pathogenic Biology, School of Basic Medical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, Shandong 250012, China.ORCID 0009-0001-6226-6854
Hua CongDepartment of Pathogenic Biology, School of Basic Medical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, Shandong 250012, China.ORCID 0000-0002-2831-4496
Juncheng WangAdvanced Medical Research Institute, Cheeloo College of Medicine, Shandong University, Jinan, Shandong 250012, China.
Chunxue ZhouDepartment of Pathogenic Biology, School of Basic Medical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, Shandong 250012, China.ORCID 0009-0007-5878-138X
Huaiyu ZhouDepartment of Pathogenic Biology, School of Basic Medical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, Shandong 250012, China.ORCID 0000-0002-9679-5375
Louis M WeissDepartment of Pathology, Albert Einstein College of Medicine, New York, NY 10461.
Hongnan QuDepartment of Pathogenic Biology, School of Basic Medical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, Shandong 250012, China.ORCID 0000-0002-1761-2068
Bing HanDepartment of Pathogenic Biology, School of Basic Medical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, Shandong 250012, China.ORCID 0000-0002-7299-2753

Funding

Microsporidia: invasion apparatusR01AI124753 · NIAID · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI WEISS, LOUIS M. · 2016 to 2025
$4.2M
GDSTC | Basic and Applied Basic Research Foundation of Guangdong Province () 2023A1515110681GDSTC | Basic and Applied Basic Research Foundation of Guangdong Province () 2024A1515010685HHS | NIH | National Institute of Allergy and Infectious Diseases (NIAID) AI124753MOST | National Natural Science Foundation of China (NSFC) 32000106MOST | National Natural Science Foundation of China (NSFC) 81971960| Natural Science Foundation of Shandong Province () ZR2023QC236NIAID NIH HHS R01 AI124753The QILU Young Scholars Program of Shandong University 21510082063092
6 · The paper itself

Abstract

Microsporidia are intracellular eukaryotic pathogens that pose a substantial threat to immunocompromised hosts. The way these pathogens manipulate host cells during infection remains poorly understood. Using a proximity biotinylation strategy we established that microsporidian EnP1 is a nucleus-targeted effector that modifies the host cell environment. EnP1's translocation to the host nucleus is meditated by nuclear localization signals (NLSs). In the nucleus, EnP1 interacts with host histone H2B. This interaction disrupts H2B monoubiquitination (H2Bub), subsequently impacting p53 expression. Crucially, this inhibition of p53 weakens its control over the downstream target gene SLC7A11, enhancing the host cell's resilience against ferroptosis during microsporidian infection. This favorable condition promotes the proliferation of microsporidia within the host cell. These findings shed light on the molecular mechanisms by which microsporidia modify their host cells to facilitate their survival.

Indexed as

FerroptosisHistonesMicrosporidiaUbiquitinationAmino Acid Transport System y+AnimalsCell NucleusFungal ProteinsHost-Pathogen InteractionsHumansMicrosporidiosisTumor Suppressor Protein p53Amino Acid Transport System y+Fungal ProteinsHistonesTumor Suppressor Protein p53EnP1ferroptosishistone H2Bmicrosporidianucleus-targeted effector

Identifiers

PMID39141344
PMCPMC11348272

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.