Evidence map›Paper›PMID 40562750›Full record

ArticleNature communications2025

Structure of lymphostatin, a large multi-functional virulence factor of pathogenic Escherichia coli.

Matthias Griessmann, Tim Rasmussen, Vanessa J Flegler, Christian Kraft, Ronja Schneider, Max Hateley, Lukas Spantzel, Mark P Stevens, Michael Börsch, Bettina Böttcher

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 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

10 authors.

Matthias GriessmannUniversity of Würzburg, Rudolf Virchow Center and Biocenter, Würzburg, Germany.ORCID http://orcid.org/0000-0001-9883-8415
Tim RasmussenUniversity of Würzburg, Rudolf Virchow Center and Biocenter, Würzburg, Germany.ORCID http://orcid.org/0000-0003-1126-846X
Vanessa J FleglerUniversity of Würzburg, Rudolf Virchow Center and Biocenter, Würzburg, Germany.
Christian KraftUniversity of Würzburg, Rudolf Virchow Center and Biocenter, Würzburg, Germany.
Ronja SchneiderUniversity of Würzburg, Rudolf Virchow Center and Biocenter, Würzburg, Germany.ORCID http://orcid.org/0009-0000-6663-5752
Max HateleyUniversity of Edinburgh, The Roslin Institute and Royal (Dick) School of Veterinary Studies, Edinburgh, UK.
Lukas SpantzelJena University Hospital, Single Molecule Microscopy Group, Jena, Germany.ORCID http://orcid.org/0000-0002-2455-8813
Mark P StevensUniversity of Edinburgh, The Roslin Institute and Royal (Dick) School of Veterinary Studies, Edinburgh, UK.
Michael BörschJena University Hospital, Single Molecule Microscopy Group, Jena, Germany.ORCID http://orcid.org/0000-0002-0634-2963
Bettina BöttcherUniversity of Würzburg, Rudolf Virchow Center and Biocenter, Würzburg, Germany. bettina.boettcher@uni-wuerzburg.de.ORCID http://orcid.org/0000-0002-7962-4849

Funding

Deutsche Forschungsgemeinschaft (German Research Foundation) 359471283Deutsche Forschungsgemeinschaft (German Research Foundation) 411346541Deutsche Forschungsgemeinschaft (German Research Foundation) 428774170Deutsche Forschungsgemeinschaft (German Research Foundation) 456578072Deutsche Forschungsgemeinschaft (German Research Foundation) 525040890RCUK | Biotechnology and Biological Sciences Research Council (BBSRC) BBS/E/RL/230002C
6 · The paper itself

Abstract

Lymphostatin is a key virulence factor of enteropathogenic and enterohaemorrhagic Escherichia coli, playing roles in bacterial colonisation of the gut and in the inhibition of lymphocyte proliferation and proinflammatory responses. The protein's glycosyltransferase and cysteine protease motifs are required for activity against lymphocytes, but high-resolution structural information has proven elusive. Here, we describe the structure of lymphostatin from enteropathogenic E. coli O127:H6, determined by electron cryo-microscopy at different pH values. We observe three conformations of a highly complex molecule with two glycosyltransferase domains, one PaToxP-like protease domain, an ADP-ribosyltransferase domain, a vertex domain and a delivery domain. Long linkers hold these domains together and occlude the catalytic sites of the N-terminal glycosyltransferase and protease domains. Lymphostatin binds to bovine T-lymphocytes and HEK-293T cells, forming clusters at the plasma membrane that are internalized. With six distinct domains, lymphostatin can be regarded as a multitool of pathogenic Escherichia coli, enabling complex interactions with host cells.

Indexed as

Enteropathogenic Escherichia coliEscherichia coliEscherichia coli ProteinsVirulence FactorsAnimalsCattleCryoelectron MicroscopyHEK293 CellsHumansModels, MolecularProtein DomainsT-LymphocytesEscherichia coli ProteinsVirulence Factors

Identifiers

PMID40562750
PMCPMC12198386

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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.