Evidence map›Paper›PMID 29347990›Full record

ArticleParasites & vectors2018

Establishment of an in vitro chicken epithelial cell line model to investigate Eimeria tenella gamete development.

Françoise I Bussière, Alisson Niepceron, Alix Sausset, Evelyne Esnault, Anne Silvestre, Robert A Walker, Nicholas C Smith, Pascale Quéré, Fabrice Laurent

Open access · goldAbstract read
In one paragraph

Article in Parasites & vectors, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
5.6field-weighted citation impact, top 4% 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

27 citing papers in PubMed, 47 citations in OpenAlex.

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  3. Novel organoids andParasitology · 2025
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  14. Article
  15. In Vitro Assessment of Anticoccidials: Methods and Molecules.Animals : an open access journal from MDPI · 2021
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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 at 4 institutions in 3 countries.

Françoise I BussièreISP, INRA, Université François Rabelais de Tours, UMR 1282, 37380, Nouzilly, France. Francoise.Bussiere@inra.fr.
Alisson NiepceronISP, INRA, Université François Rabelais de Tours, UMR 1282, 37380, Nouzilly, France.
Alix SaussetISP, INRA, Université François Rabelais de Tours, UMR 1282, 37380, Nouzilly, France.
Evelyne EsnaultISP, INRA, Université François Rabelais de Tours, UMR 1282, 37380, Nouzilly, France.
Anne SilvestreISP, INRA, Université François Rabelais de Tours, UMR 1282, 37380, Nouzilly, France.
Robert A WalkerInstitute of Parasitology, University of Zurich, Winterthurerstrasse 266a, CH-8057, Zurich, Switzerland.
Nicholas C SmithResearch School of Biology, Australian National University, Canberra, ACT, 2601, Australia.
Pascale QuéréISP, INRA, Université François Rabelais de Tours, UMR 1282, 37380, Nouzilly, France.
Fabrice LaurentISP, INRA, Université François Rabelais de Tours, UMR 1282, 37380, Nouzilly, France.
Infectiologie Animale et Santé Publique · FRUniversité de Tours · FRAustralian National University · AUUniversity of Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEimeria tenella infection leads to acute intestinal disorders responsible for important economic losses in poultry farming worldwide. The life-cycle of E. tenella is monoxenous with the chicken as the exclusive host; infection occurs in caecal epithelial cells. However, in vitro, the complete life-cycle of the parasite has only been propagated successfully in primary chicken kidney cells, which comprise undefined mixed cell populations; no cell line model has been able to consistently support the development of the sexual stages of the parasite. We therefore sought to develop a new model to study E. tenella gametogony in vitro using a recently characterised chicken cell line (CLEC-213) exhibiting an epithelial cell phenotype.

methodsCLEC-213 were infected with sporozoites from a precocious strain or with second generation merozoites (merozoites II) from wild type strains. Sexual stages of the parasite were determined both at the gene and protein levels.

resultsTo our knowledge, we show for the first time in CLEC-213, that sporozoites from a precocious strain of E. tenella were able to develop to gametes, as verified by measuring gene expression and by using antibodies to a microgamete-specific protein (EtFOA1: flagellar outer arm protein 1) and a macrogamete-specific protein (EtGAM-56), but oocysts were not observed. However, both gametes and oocysts were observed when cells were infected with merozoites II from wild type strains, demonstrating that completion of the final steps of the parasite cycle is possible in CLEC-213 cells.

conclusionThe epithelial cell line CLEC-213 constitutes a useful avian tool for studying Eimeria epithelial cell interactions and the effect of drugs on E. tenella invasion, merogony and gametogony.

Indexed as

Models, BiologicalAnimalsCell LineChickensCoccidiosisEimeria tenellaEpithelial CellsGerm CellsChicken epithelial cellsEimeria tenellaMacrogametesMicrogametes

Identifiers

PMID29347990
PMCPMC5774133
OpenAlexW2790475117

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.