Evidence map›Paper›PMID 31619276›Full record

ArticleParasites & vectors2019

Disruption of gut integrity and permeability contributes to enteritis in a fish-parasite model: a story told from serum metabolomics.

Ariadna Sitjà-Bobadilla, Rubén Gil-Solsona, Itziar Estensoro, M Carla Piazzon, Juan Antonio Martos-Sitcha, Amparo Picard-Sánchez, Juan Fuentes, Juan Vicente Sancho, Josep A Calduch-Giner, Félix Hernández and 1 more

Open access · goldAbstract read
In one paragraph

Article in Parasites & vectors, 2019. 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
4.0field-weighted citation impact, top 6% 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

12 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Detection and Identification ofPathogens (Basel, Switzerland) · 2026
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  3. Methanotroph (Animal nutrition (Zhongguo xu mu shou yi xue hui) · 2025
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  4. Article
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  8. Review
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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

11 authors at 4 institutions in 2 countries.

Ariadna Sitjà-BobadillaFish Pathology Group, Instituto de Acuicultura Torre de la Sal (IATS-CSIC), 12595 Ribera de Cabanes, Castellón, Spain. ariadna.sitja@csic.es.ORCID http://orcid.org/0000-0002-7473-3413
Rubén Gil-SolsonaResearch Institute for Pesticides and Water (IUPA), University Jaume I, Avda. Vicent Sos Baynat, s/n. Campus del Riu Sec, 12071, Castellón, Spain.
Itziar EstensoroFish Pathology Group, Instituto de Acuicultura Torre de la Sal (IATS-CSIC), 12595 Ribera de Cabanes, Castellón, Spain.
M Carla PiazzonFish Pathology Group, Instituto de Acuicultura Torre de la Sal (IATS-CSIC), 12595 Ribera de Cabanes, Castellón, Spain.
Juan Antonio Martos-SitchaNutrigenomics and Fish Endocrinology Group, Instituto de Acuicultura Torre de la Sal (IATS-CSIC), 12595 Ribera de Cabanes, Castellón, Spain.
Amparo Picard-SánchezFish Pathology Group, Instituto de Acuicultura Torre de la Sal (IATS-CSIC), 12595 Ribera de Cabanes, Castellón, Spain.
Juan FuentesComparative Endocrinology and Integrative Biology, CCMar, University of Algarve, Campus de Gambelas, 8005-139, Faro, Portugal.
Juan Vicente SanchoResearch Institute for Pesticides and Water (IUPA), University Jaume I, Avda. Vicent Sos Baynat, s/n. Campus del Riu Sec, 12071, Castellón, Spain.
Josep A Calduch-GinerAssociated Unit of Marine Ecotoxicology (IATS-IUPA), Castellon, Spain.
Félix HernándezAssociated Unit of Marine Ecotoxicology (IATS-IUPA), Castellon, Spain.
Jaume Pérez-SánchezAssociated Unit of Marine Ecotoxicology (IATS-IUPA), Castellon, Spain.
Instituto de Acuicultura Torre de la Sal · ESUniversitat Jaume I · ESUniversidad de Cádiz · ESUniversity of Algarve · PT

Funding

CANCER AND LEUKEMIA GROUP B (CALGB)U10CA004326 · NCI · DARTMOUTH COLLEGE · PI ERNSTOFF, MARC S · 1985 to 2002
$546k
Consejo Superior de Investigaciones Científicas PIE 201740E013Conselleria d'Educació, Investigació, Cultura i Esport APOSTD/2016/037Fundação para a Ciência e a Tecnologia UID/Multi 04326/2019H2020 Research Infrastructures 652831H2020 Research Infrastructures TNA AE10004-INTEBREAMH2020 Societal Challenges 634429Ministerio de Economía, Industria y Competitividad, Gobierno de España AGL2013-48560-C2-1-RMinisterio de Economía, Industria y Competitividad, Gobierno de España AGL2013-48560-C2-2-R
6 · The paper itself

Abstract

backgroundIn the animal production sector, enteritis is responsible for serious economic losses, and intestinal parasitism is a major stress factor leading to malnutrition and lowered performance and animal production efficiency. The effect of enteric parasites on the gut function of teleost fish, which represent the most ancient bony vertebrates, is far from being understood. The intestinal myxozoan parasite Enteromyxum leei dwells between gut epithelial cells and causes severe enteritis in gilthead sea bream (Sparus aurata), anorexia, cachexia, growth impairment, reduced marketability and increased mortality.

methodsThis study aimed to outline the gut failure in this fish-parasite model using a multifaceted approach and to find and validate non-lethal serum markers of gut barrier dysfunction. Intestinal integrity was studied in parasitized and non-parasitized fish by immunohistochemistry with specific markers for cellular adhesion (E-cadherin) and tight junctions (Tjp1 and Cldn3) and by functional studies of permeability (oral administration of FITC-dextran) and electrophysiology (Ussing chambers). Serum samples from parasitized and non-parasitized fish were analyzed using non-targeted metabolomics and some significantly altered metabolites were selected to be validated using commercial kits.

resultsThe immunodetection of Tjp1 and Cldn3 was significantly lower in the intestine of parasitized fish, while no strong differences were found in E-cadherin. Parasitized fish showed a significant increase in paracellular uptake measured by FITC-dextran detection in serum. Electrophysiology showed a decrease in transepithelial resistance in infected animals, which showed a diarrheic profile. Serum metabolomics revealed 3702 ions, from which the differential expression of 20 identified compounds significantly separated control from infected groups in multivariate analyses. Of these compounds, serum inosine (decreased) and creatine (increased) were identified as relevant and validated with commercial kits.

conclusionsThe results demonstrate the disruption of tight junctions and the loss of gut barrier function, a metabolomic profile of absorption dysfunction and anorexia, which further outline the pathophysiological effects of E. leei.

Indexed as

MetabolomicsAnimalsCadherinsClaudin-3CreatineDextransDisease Models, AnimalElectrophysiologyEnteritisEnzyme-Linked Immunosorbent AssayFish DiseasesFluorescein-5-isothiocyanateImmunohistochemistryInosineIntestinal MucosaIntestinesCadherinsClaudin-3CreatineDextransFluorescein-5-isothiocyanatefluorescein isothiocyanate dextranInosineZonula Occludens-1 ProteinAquacultureElectrophysiologyEnteromyxum leeiGilthead sea breamGut barrierMetabolomicsMyxozoaPathophysiologyTeleosteiTight junctions

Identifiers

PMID31619276
PMCPMC6796429
OpenAlexW2981016854

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.