Evidence map›Paper›PMID 35365634›Full record

ArticleNature communications2022

Defining the early stages of intestinal colonisation by whipworms.

María A Duque-Correa, David Goulding, Faye H Rodgers, J Andrew Gillis, Claire Cormie, Kate A Rawlinson, Allison J Bancroft, Hayley M Bennett, Magda E Lotkowska, Adam J Reid and 17 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
7.3field-weighted citation impact, top 2% of its field
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

24 citing papers in PubMed, 47 citations in OpenAlex.

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  10. Advances in Single-Cell Sequencing for Infectious Diseases: Progress and Perspectives.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
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  15. Review
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  20. Review
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

27 authors at 7 institutions in 3 countries.

María A Duque-CorreaWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, CB10 1SA, UK. md19@sanger.ac.uk.ORCID http://orcid.org/0000-0002-0567-0412
David Goulding *Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, CB10 1SA, UK.
Faye H Rodgers *Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, CB10 1SA, UK.
J Andrew GillisDepartment of Zoology, University of Cambridge, Cambridge, CB2 3EJ, UK.
Claire CormieWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, CB10 1SA, UK.
Kate A RawlinsonWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, CB10 1SA, UK.ORCID http://orcid.org/0000-0001-8297-8405
Allison J BancroftLydia Becker Institute of Immunology and Inflammation, Wellcome Trust Centre for Cell Matrix Research and Faculty of Biology, Medicine and Health, University of Manchester, Manchester, M13 9PT, UK.
Hayley M BennettWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, CB10 1SA, UK.ORCID http://orcid.org/0000-0001-8879-2855
Magda E LotkowskaWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, CB10 1SA, UK.
Adam J ReidWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, CB10 1SA, UK.ORCID http://orcid.org/0000-0002-5926-7768
Anneliese O SpeakWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, CB10 1SA, UK.ORCID http://orcid.org/0000-0003-4890-4685
Paul ScottWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, CB10 1SA, UK.
Nicholas RedshawWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, CB10 1SA, UK.
Charlotte TolleyWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, CB10 1SA, UK.ORCID http://orcid.org/0000-0002-1119-7983
Catherine McCarthyWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, CB10 1SA, UK.
Cordelia BrandtWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, CB10 1SA, UK.
Catherine SharpeLydia Becker Institute of Immunology and Inflammation, Wellcome Trust Centre for Cell Matrix Research and Faculty of Biology, Medicine and Health, University of Manchester, Manchester, M13 9PT, UK.
Caroline RidleyLydia Becker Institute of Immunology and Inflammation, Wellcome Trust Centre for Cell Matrix Research and Faculty of Biology, Medicine and Health, University of Manchester, Manchester, M13 9PT, UK.
Judit Gali MoyaFaculty of Biology, University of Barcelona, Barcelona, 08028, Spain.
Claudia M CarneiroImmunopathology Laboratory, NUPEB, Federal University of Ouro Preto, Campus Universitario Morro do Cruzeiro, Ouro Preto, MG, 35400-000, Brazil.ORCID http://orcid.org/0000-0002-6002-857X
Tobias StarborgLydia Becker Institute of Immunology and Inflammation, Wellcome Trust Centre for Cell Matrix Research and Faculty of Biology, Medicine and Health, University of Manchester, Manchester, M13 9PT, UK.
Kelly S HayesLydia Becker Institute of Immunology and Inflammation, Wellcome Trust Centre for Cell Matrix Research and Faculty of Biology, Medicine and Health, University of Manchester, Manchester, M13 9PT, UK.ORCID http://orcid.org/0000-0003-3034-048X
Nancy HolroydWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, CB10 1SA, UK.
Mandy SandersWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, CB10 1SA, UK.
David J ThorntonLydia Becker Institute of Immunology and Inflammation, Wellcome Trust Centre for Cell Matrix Research and Faculty of Biology, Medicine and Health, University of Manchester, Manchester, M13 9PT, UK.ORCID http://orcid.org/0000-0001-7148-1970
Richard K GrencisLydia Becker Institute of Immunology and Inflammation, Wellcome Trust Centre for Cell Matrix Research and Faculty of Biology, Medicine and Health, University of Manchester, Manchester, M13 9PT, UK.ORCID http://orcid.org/0000-0002-7592-0085
Matthew BerrimanWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, CB10 1SA, UK. mb4@sanger.ac.uk.ORCID http://orcid.org/0000-0002-9581-0377
Wellcome Sanger Institute · GBWellcome Centre for Cell-Matrix Research · GBUniversity of Cambridge · GBEnvironment Agency · GBThe Gurdon Institute · GBUniversidade Federal de Ouro Preto · BRUniversitat de Barcelona · ES

Funding

Medical Research Council MR/R002800/1Wellcome Trust 088785/Z/09/ZWellcome Trust 206194Wellcome Trust 210661/Z/18/ZWellcome Trust Z10661/Z/18/Z
6 · The paper itself

Abstract

Whipworms are large metazoan parasites that inhabit multi-intracellular epithelial tunnels in the large intestine of their hosts, causing chronic disease in humans and other mammals. How first-stage larvae invade host epithelia and establish infection remains unclear. Here we investigate early infection events using both Trichuris muris infections of mice and murine caecaloids, the first in-vitro system for whipworm infection and organoid model for live helminths. We show that larvae degrade mucus layers to access epithelial cells. In early syncytial tunnels, larvae are completely intracellular, woven through multiple live dividing cells. Using single-cell RNA sequencing of infected mouse caecum, we reveal that progression of infection results in cell damage and an expansion of enterocytes expressing of Isg15, potentially instigating the host immune response to the whipworm and tissue repair. Our results unravel intestinal epithelium invasion by whipworms and reveal specific host-parasite interactions that allow the whipworm to establish its multi-intracellular niche.

Indexed as

HelminthsTrichuriasisAnimalsIntestinal MucosaIntestinesMammalsMiceTrichuris

Identifiers

PMID35365634
PMCPMC8976045
OpenAlexW4220953001

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.