Evidence map›Paper›PMID 42029767›Full record

ArticleMolecular genetics and genomics : MGG2026

Pangenomic and functional domain comparison of enterotoxigenic Escherichia coli isolated from humans and swine: insights into host specificity.

Gabriela Merker Breyer, Juliana Silva Bernardes, Márcio Dorn, Franciele Maboni Siqueira

Abstract readComparative Study
In one paragraph

Article in Molecular genetics and genomics : MGG, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Gabriela Merker BreyerLaboratório de Bacteriologia Veterinária (LaBacVet), Departamento de Patologia Veterinária, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
Juliana Silva BernardesStation Biologique de Roscoff, Roscoff, France.
Márcio DornCentro de Biotecnologia (CBiot), Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
Franciele Maboni SiqueiraLaboratório de Bacteriologia Veterinária (LaBacVet), Departamento de Patologia Veterinária, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil. franciele.siqueira@ufrgs.br.ORCID http://orcid.org/0000-0001-7282-6117

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diarrhea caused by enterotoxigenic Escherichia coli (ETEC) is a common threat to humans and animals. Clinical ETEC strains display host tropism, usually driven by adherence and toxin-host interactions in the gut. Other virulence factors, metal acquisition mechanisms, and immune evasion strategies may also influence host specificity. Using publicly available genomes, we performed a pangenomic and functional comparison of 77 human- and swine-derived ETEC strains. Sequence types ST10 and ST4 found in both hosts, suggesting potential cross-host transmission. Phylogenetic analyses showed clustering mainly by ST, regardless of host or geography. Additionally, most functional domains were shared between hosts; however, human-derived strains carried exclusive domains related to adhesion, transposition, and toxins, whereas swine-derived strains harbored domains linked to stress response and metal binding. Notably, the PF09075 domain from the STb enterotoxin occurred only in swine-derived strains, despite previous reports in humans. Comparative analyses of STa (PF02048) and STb revealed no structural or functional homology but confirmed the swine-specific association of STb and greater sequence STa variability in human-derived strains. These findings indicate that sequence and functional differences in these enterotoxins contribute to ETEC host tropism, while ST patterns reveal possible epidemiological links between human and swine infections.

Indexed as

Enterotoxigenic Escherichia coliEscherichia coli InfectionsGenome, BacterialHost SpecificityAnimalsBacterial ToxinsEnterotoxinsEscherichia coli ProteinsHost TropismHumansPhylogenyProtein DomainsSwineVirulence FactorsBacterial ToxinsEnterotoxinsEscherichia coli ProteinsVirulence FactorsETECFunctional domainsHost specificityPangenome analysis

Identifiers

PMID42029767
PMCPMC13109261

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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.