Evidence map›Paper›PMID 41803683›Full record

ArticleBMC genomics2026

Transcriptome profiling of intra-snail stages of the liver fluke Fasciola hepatica reveals key mediators underlying parasite development and interaction with the host.

Mauricio Langleib, Santiago Fontenla, Fernanda Domínguez, Geetha Sankaranarayanan, Sabina Wlodek, Matt Berriman, Gabriel Rinaldi, Andrés Iriarte, José F Tort

Abstract read
In one paragraph

Article in BMC genomics, 2026. 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

9 authors.

Mauricio LangleibLaboratorio de Biología Computacional, Departamento de Desarrollo Biotecnológico, Instituto de Higiene, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay.
Santiago FontenlaDepartamento de Genética, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay.
Fernanda DomínguezDepartamento de Genética, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay.
Geetha SankaranarayananWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
Sabina WlodekDepartamento de Genética, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay.
Matt BerrimanWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
Gabriel RinaldiWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
Andrés IriarteLaboratorio de Biología Computacional, Departamento de Desarrollo Biotecnológico, Instituto de Higiene, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay. airiarte@higiene.edu.uy.
José F TortDepartamento de Genética, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay. jtort@fmed.edu.uy.

Funding

Agencia Nacional de Investigación e Innovación FCE-3-2016-1-125297Comisión Sectorial de Investigación Científica I+D-2016-516UK Research and Innovation MR/W013568/1Wellcome Trust 206194
6 · The paper itself

Abstract

backgroundWhile mammalian host invasion by the liver fluke Fasciola hepatica has been extensively studied, reports on the interaction with its intermediate host at the molecular level remain scarce. These developmental stages are particularly interesting since at least two cycles of asexual amplification occur within lymnaeid snails, leading to the production of hundreds of infective metacercariae. We analyzed transcriptomic data from miracidia and intra-molluscan stages seeking clues of these interaction and developmental processes.

resultsWe identified 1744 novel transcripts and several isoforms of already annotated genes. Analysis of expression across the whole life cycle resulted in five distinct gene expression clusters (egg, miracidia, intra-snail stages, invading stages and juvenile-adults). Few genes showed strict stage-specific expression, but notably most of those corresponding to miracidial and intra-snail stages were novel unannotated genes. Genes upregulated in the miracidium include enzymes involved in neurotransmitter synthesis, energy metabolism and calcium mediated signaling, consistent with the physiology of a short-lived free-living stage. Several genes associated with development and morphogenesis were characterized in early (15 days post-infection) intra-snail stages. Purine salvage pathway genes were upregulated in this time-point, consistent with a high biosynthetic demand and the absence of a complete purine synthesis pathway in F. hepatica. Mucins, glycan biosynthesis genes and aquaporins upregulated within late (30 dpi) intra-snail stages are interesting, considering their putative role in the next host transition.

conclusionsDifferent members of well-known protein families involved in host-parasite interaction such as cathepsin proteases, legumains, protease inhibitors and lipid transporters were detected with stage specific expression in early and late intra-snail stages. These findings suggest duplication and tunning during evolution of the same set of molecular mediators for the interactions with the intermediate and definitive hosts.

Indexed as

Fasciola hepaticaGene Expression ProfilingHost-Parasite InteractionsTranscriptomeAnimalsLife Cycle StagesDevelopmentFasciolaGene familiesIntermediate hostInvasionTranscriptomics

Identifiers

PMID41803683
PMCPMC12983594

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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.