Evidence map›Paper›PMID 39160174›Full record

ArticleNature communications2024

Host-pathogen interactions in the Plasmodium-infected mouse liver at spatial and single-cell resolution.

Franziska Hildebrandt, Miren Urrutia Iturritza, Christian Zwicker, Bavo Vanneste, Noémi Van Hul, Elisa Semle, Jaclyn Quin, Tales Pascini, Sami Saarenpää, Mengxiao He and 5 more

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Single-cell sequencing: accurate disease detection.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
  7. Article
  8. Review
  9. Article
  10. Advances in Single-Cell Sequencing for Infectious Diseases: Progress and Perspectives.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
  11. Review
  12. 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

15 authors.

Franziska HildebrandtMolecular Biosciences, the Wenner Gren Institute, Stockholm University, Svante Arrhenius Väg 20C, SE-106 91, Stockholm, Sweden. franziska.hildebrandt@su.se.ORCID 0000-0002-2673-1704
Miren Urrutia IturritzaMolecular Biosciences, the Wenner Gren Institute, Stockholm University, Svante Arrhenius Väg 20C, SE-106 91, Stockholm, Sweden.ORCID 0000-0002-3989-1803
Christian ZwickerDepartment of Biomedical Molecular Biology, Faculty of Sciences, Ghent University, Ghent, Belgium.
Bavo VannesteDepartment of Biomedical Molecular Biology, Faculty of Sciences, Ghent University, Ghent, Belgium.
Noémi Van HulDepartment of Cell and Molecular Biology, Karolinska Institutet Stockholm, SE-171 77, Solna, Sweden.ORCID 0000-0003-1410-8808
Elisa SemleMolecular Biosciences, the Wenner Gren Institute, Stockholm University, Svante Arrhenius Väg 20C, SE-106 91, Stockholm, Sweden.
Jaclyn QuinMolecular Biosciences, the Wenner Gren Institute, Stockholm University, Svante Arrhenius Väg 20C, SE-106 91, Stockholm, Sweden.
Tales PasciniLaboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, 12735 Twinbrook Parkway, Rm 2E20A, Rockville, MD, 20852, USA.
Sami SaarenpääSciLifeLab, Department of Gene Technology, KTH Royal Institute of Technology, Tomtebodavägen 23a, SE-171 65, Solna, Sweden.ORCID 0000-0003-4731-6857
Mengxiao HeSciLifeLab, Department of Gene Technology, KTH Royal Institute of Technology, Tomtebodavägen 23a, SE-171 65, Solna, Sweden.ORCID 0000-0001-5905-8467
Emma R AnderssonDepartment of Cell and Molecular Biology, Karolinska Institutet Stockholm, SE-171 77, Solna, Sweden.ORCID 0000-0002-8608-625X
Charlotte L ScottDepartment of Biomedical Molecular Biology, Faculty of Sciences, Ghent University, Ghent, Belgium.ORCID 0000-0003-4914-6580
Joel Vega-RodriguezLaboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, 12735 Twinbrook Parkway, Rm 2E20A, Rockville, MD, 20852, USA.ORCID 0000-0002-9576-0058
Joakim LundebergSciLifeLab, Department of Gene Technology, KTH Royal Institute of Technology, Tomtebodavägen 23a, SE-171 65, Solna, Sweden.ORCID 0000-0003-4313-1601
Johan AnkarklevMolecular Biosciences, the Wenner Gren Institute, Stockholm University, Svante Arrhenius Väg 20C, SE-106 91, Stockholm, Sweden. johan.ankarklev@su.se.ORCID 0000-0003-3170-8493

Funding

Karolinska Institutet (Karolinska Institute) 2-195/2021Svenska Sällskapet för Medicinsk Forskning (Swedish Society for Medical Research) Stora AnslaagetVetenskapsrådet (Swedish Research Council) VR 2019-01350Vetenskapsrådet (Swedish Research Council) VR 2021-05057
6 · The paper itself

Abstract

Upon infecting its vertebrate host, the malaria parasite initially invades the liver where it undergoes massive replication, whilst remaining clinically silent. The coordination of host responses across the complex liver tissue during malaria infection remains unexplored. Here, we perform spatial transcriptomics in combination with single-nuclei RNA sequencing over multiple time points to delineate host-pathogen interactions across Plasmodium berghei-infected liver tissues. Our data reveals significant changes in spatial gene expression in the malaria-infected tissues. These include changes related to lipid metabolism in the proximity to sites of Plasmodium infection, distinct inflammation programs between lobular zones, and regions with enrichment of different inflammatory cells, which we term 'inflammatory hotspots'. We also observe significant upregulation of genes involved in inflammation in the control liver tissues of mice injected with mosquito salivary gland components. However, this response is considerably delayed compared to that observed in P. berghei-infected mice. Our study establishes a benchmark for investigating transcriptome changes during host-parasite interactions in tissues, it provides informative insights regarding in vivo study design linked to infection and offers a useful tool for the discovery and validation of de novo intervention strategies aimed at malaria liver stage infection.

Indexed as

LiverMalariaPlasmodium bergheiAnimalsFemaleGene Expression ProfilingHost-Parasite InteractionsHost-Pathogen InteractionsInflammationLipid MetabolismMiceMice, Inbred C57BLSingle-Cell AnalysisTranscriptome

Identifiers

PMID39160174
PMCPMC11333755

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.