Evidence map›Paper›PMID 40188181›Full record

ArticleNature communications2025

scRNA-seq uncovers the transcriptional dynamics of Encephalitozoon intestinalis parasites in human macrophages.

Pattana Jaroenlak, Kacie L McCarty, Bo Xia, Cherry Lam, Erin E Zwack, Nadia L Almasri, Joseph Sudar, Maelle Aubry, Itai Yanai, Gira Bhabha and 1 more

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. Advances in Single-Cell Sequencing for Infectious Diseases: Progress and Perspectives.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Pattana Jaroenlak *Center of Excellence for Molecular Biology and Genomics of Shrimp, Department of Biochemistry, Faculty of Science, Chulalongkorn University, Bangkok, 10330, Thailand.
Kacie L McCarty *Department of Biology, Johns Hopkins University, Baltimore, MD, 21218, USA.ORCID http://orcid.org/0000-0002-5174-1904
Bo XiaBroad Institute of MIT and Harvard, Cambridge, MA, 02142, USA.ORCID http://orcid.org/0000-0003-0929-7253
Cherry LamDepartment of Cell Biology, New York University Grossman School of Medicine, New York, 10016, USA.
Erin E ZwackDepartment of Microbiology, New York University Grossman School of Medicine, New York, 10016, USA.
Nadia L AlmasriDepartment of Biology, Johns Hopkins University, Baltimore, MD, 21218, USA.ORCID http://orcid.org/0009-0003-8064-1376
Joseph SudarVilcek Institute of Graduate Biomedical Sciences, NYU School of Medicine, New York, NY, 10016, USA.ORCID http://orcid.org/0000-0002-0112-1934
Maelle AubryDepartment of Cell Biology, New York University Grossman School of Medicine, New York, 10016, USA.ORCID http://orcid.org/0009-0008-5973-8372
Itai YanaiDepartment of Biochemistry and Molecular Pharmacology, New York University Grossman School of Medicine, New York, NY, 10016, USA.ORCID http://orcid.org/0000-0002-8438-2741
Gira BhabhaDepartment of Cell Biology, New York University Grossman School of Medicine, New York, 10016, USA. gira.bhabha@jhu.edu.ORCID http://orcid.org/0000-0003-0624-6178
Damian C EkiertDepartment of Cell Biology, New York University Grossman School of Medicine, New York, 10016, USA. dekiert1@jh.edu.ORCID http://orcid.org/0000-0002-2570-0404

Funding

Structural basis of the polar tube invasion machinery from microsporidia parasitesR01AI147131 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI BHABHA, GIRA · 2020 to 2024
$3.4M
NIAID NIH HHS R01 AI147131U.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases (NIAID) 1F31AI183707U.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases (NIAID) R01AI147131
6 · The paper itself

Abstract

Microsporidia are single-celled intracellular parasites that cause opportunistic diseases in humans. Encephalitozoon intestinalis is a prevalent human-infecting species that invades the small intestine. Macrophages are potential reservoirs of infection, and dissemination to other organ systems is also observed. The macrophage response to infection and the developmental trajectory of the parasite are not well studied. Here we use single cell RNA sequencing to investigate transcriptional changes in both the parasite and the host during E. intestinalis infection of human macrophages in vitro. The parasite undergoes large transcriptional changes throughout the life cycle, providing a blueprint for parasite development. While a small population of infected macrophages mount a response, most remain transcriptionally unchanged, suggesting that the majority of parasites may avoid host detection. The stealthy microsporidian lifestyle likely allows these parasites to harness macrophages for replication. Together, our data provide insights into the host response in primary human macrophages and the E. intestinalis developmental program.

Indexed as

EncephalitozoonEncephalitozoonosisMacrophagesHost-Parasite InteractionsHumansRNA-SeqSingle-Cell AnalysisSingle-Cell Gene Expression AnalysisTranscription, GeneticTranscriptome

Identifiers

PMID40188181
PMCPMC11972355

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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 Socratic graph.