Evidence mapPaperPMID 41527151Full record

ArticleMicrobiome2026

Increased caecal Intestinimonas abundance inhibits E. tenella gametogenesis via EtGFAT regulation and alleviates infection through immunity.

Jun-Yi Li, Hai-Bin Huang, Chun-Wei Shi, Tian-Xu Pan, Ming-Han Li, Nan Wang, Jia-Jin Shan, Yan-Long Jiang, Wen-Tao Yang, Xin Cao and 5 more

Abstract read
In one paragraph

Article in Microbiome, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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

15 authors.

Jun-Yi Li *College of Veterinary Medicine, Jilin Agricultural University, Changchun, 130118, China.
Hai-Bin Huang *College of Veterinary Medicine, Jilin Agricultural University, Changchun, 130118, China.
Chun-Wei Shi *College of Veterinary Medicine, Jilin Agricultural University, Changchun, 130118, China.
Tian-Xu PanCollege of Veterinary Medicine, Jilin Agricultural University, Changchun, 130118, China.
Ming-Han LiCollege of Veterinary Medicine, Jilin Agricultural University, Changchun, 130118, China.
Nan WangCollege of Veterinary Medicine, Jilin Agricultural University, Changchun, 130118, China.
Jia-Jin ShanCollege of Veterinary Medicine, Jilin Agricultural University, Changchun, 130118, China.
Yan-Long JiangCollege of Veterinary Medicine, Jilin Agricultural University, Changchun, 130118, China.
Wen-Tao YangCollege of Veterinary Medicine, Jilin Agricultural University, Changchun, 130118, China.
Xin CaoCollege of Veterinary Medicine, Jilin Agricultural University, Changchun, 130118, China.
Jian-Zhong WangCollege of Veterinary Medicine, Jilin Agricultural University, Changchun, 130118, China.
Jia-Yao GuanCollege of Veterinary Medicine, Jilin Agricultural University, Changchun, 130118, China.
Shu-Yuan YuCollege of Veterinary Medicine, Jilin Agricultural University, Changchun, 130118, China.
Chun-Feng WangCollege of Veterinary Medicine, Jilin Agricultural University, Changchun, 130118, China. wangchunfeng@jlau.edu.cn.
Gui-Lian YangCollege of Veterinary Medicine, Jilin Agricultural University, Changchun, 130118, China. yangguilian@jlau.edu.cn.

Funding

National Natural Science Foundation of China 32072888, U21A20261, 32202819
6 · The paper itself

Abstract

backgroundChicken coccidiosis caused by Eimeria tenella (E. tenella) poses a major threat to global poultry production, with its tropism for the caecal microenvironment and dynamic interactions with the resident microbiota remaining incompletely understood. The caecal microbiota plays a critical role in host‒parasite interplay, yet the mechanisms through which microbial homeostasis influences E. tenella development and host resistance remain elusive. This study aimed to elucidate the causal relationship between caecal dysbiosis and E. tenella pathogenesis, with a focus on identifying microbiota-derived regulators of parasite development and host immunity.

resultsAntibiotic-induced caecal dysbiosis (ABX) significantly impaired E. tenella macrogametogenesis, demonstrating microbiota-dependent regulation of parasitic development. Faecal microbiota transplantation (FMT) validated this causal link, revealing that microbial reconstitution restored parasite maturation. Notably, Intestinimonas spp. were identified as key inhibitors of E. tenella development through transcriptional regulation of the EtGFAT gene (Eimeria tenella glucosamine: fructose-6-phosphate aminotransferase), a critical mediator of macrogamete formation. Furthermore, the transplantation of Intestinimonas butyriciproducens (I. butyriciproducens) attenuated clinical manifestations of infection while increasing IFN-γ secretion from CD8

conclusionsThis study revealed that caecal microbiota homeostasis is indispensable for E. tenella developmental progression and highlights Intestinimonas as a pivotal microbial regulator of parasite biology. The dual role of I. butyriciproducens in suppressing parasitic virulence and potentiating adaptive immune responses underscores the therapeutic potential of microbiota-targeted strategies. These findings provide a foundation for the development of novel anticoccidial interventions through targeted manipulation of caecal microbial communities. Video Abstract.

Indexed as

CecumCoccidiosisEimeria tenellaGastrointestinal MicrobiomePoultry DiseasesAnimalsChickensDysbiosisFecal Microbiota TransplantationCaecal microbiotaCD8+ T cellsEimeria tenellaEtGFATGametogonyIntestinimonas

Identifiers

PMID41527151
PMCPMC12888579

What Socratic 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 Socratic graph.