Evidence map›Paper›PMID 39466773›Full record

ArticlePloS one2024

Fecal microbiota transplantation from protozoa-exposed donors downregulates immune response in a germ-free mouse model, its role in immune response and physiology of the intestine.

Oswaldo Partida-Rodríguez, Eric M Brown, Sarah E Woodward, Mihai Cirstea, Lisa A Reynolds, Charisse Petersen, Stefanie L Vogt, Jorge Peña-Díaz, Lisa Thorson, Marie-Claire Arrieta and 9 more

Abstract read
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Review
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

19 authors.

Oswaldo Partida-RodríguezUnidad de Investigación en Medicina Experimental, Hospital General de Mexico, Universidad Nacional Autónoma de México, Mexico, Mexico.
Eric M BrownMichael Smith Laboratories, Department of Microbiology & Immunology, University of British Columbia, Vancouver, Canada.
Sarah E WoodwardMichael Smith Laboratories, Department of Microbiology & Immunology, University of British Columbia, Vancouver, Canada.ORCID 0000-0002-6688-0595
Mihai CirsteaMichael Smith Laboratories, Department of Microbiology & Immunology, University of British Columbia, Vancouver, Canada.
Lisa A ReynoldsMichael Smith Laboratories, Department of Microbiology & Immunology, University of British Columbia, Vancouver, Canada.
Charisse PetersenMichael Smith Laboratories, Department of Microbiology & Immunology, University of British Columbia, Vancouver, Canada.
Stefanie L VogtMichael Smith Laboratories, Department of Microbiology & Immunology, University of British Columbia, Vancouver, Canada.ORCID 0000-0002-0393-5712
Jorge Peña-DíazMichael Smith Laboratories, Department of Microbiology & Immunology, University of British Columbia, Vancouver, Canada.ORCID 0000-0002-9211-240X
Lisa ThorsonMichael Smith Laboratories, Department of Microbiology & Immunology, University of British Columbia, Vancouver, Canada.
Marie-Claire ArrietaMichael Smith Laboratories, Department of Microbiology & Immunology, University of British Columbia, Vancouver, Canada.
Eric G HernándezUnidad de Investigación en Medicina Experimental, Hospital General de Mexico, Universidad Nacional Autónoma de México, Mexico, Mexico.
Liliana Rojas-VelázquezUnidad de Investigación en Medicina Experimental, Hospital General de Mexico, Universidad Nacional Autónoma de México, Mexico, Mexico.
Patricia MoranUnidad de Investigación en Medicina Experimental, Hospital General de Mexico, Universidad Nacional Autónoma de México, Mexico, Mexico.
Enrique González RivasUnidad de Investigación en Medicina Experimental, Hospital General de Mexico, Universidad Nacional Autónoma de México, Mexico, Mexico.
Angélica Serrano-VázquezUnidad de Investigación en Medicina Experimental, Hospital General de Mexico, Universidad Nacional Autónoma de México, Mexico, Mexico.
Horacio Pérez-JuárezUnidad de Investigación en Medicina Experimental, Hospital General de Mexico, Universidad Nacional Autónoma de México, Mexico, Mexico.
Javier TorresUnidad de Investigación en Enfermedades Infecciosas y Parasitarias, Instituto Mexicano del Seguro Social (IMSS), Mexico, Mexico.
Cecilia XiménezUnidad de Investigación en Medicina Experimental, Hospital General de Mexico, Universidad Nacional Autónoma de México, Mexico, Mexico.ORCID 0000-0003-0574-4538
B B FinlayMichael Smith Laboratories, Department of Microbiology & Immunology, University of British Columbia, Vancouver, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intestinal parasites are part of the intestinal ecosystem and have been shown to establish close interactions with the intestinal microbiota. However, little is known about the influence of intestinal protozoa on the regulation of the immune response. In this study, we analyzed the regulation of the immune response of germ-free mice transplanted with fecal microbiota (FMT) from individuals with multiple parasitic protozoans (P) and non-parasitized individuals (NP). We determined the production of intestinal cytokines, the lymphocyte populations in both the colon and the spleen, and the genetic expression of markers of intestinal epithelial integrity. We observed a general downregulation of the intestinal immune response in mice receiving FMT-P. We found significantly lower intestinal production of the cytokines IL-6, TNF, IFN-γ, MCP-1, IL-10, and IL-12 in the FMT-P. Furthermore, a significant decrease in the proportion of CD3+, CD4+, and Foxp3+ T regulatory cells (Treg) was observed in both, the colon and spleen with FMT-P in contrast to FMT-NP. We also found that in FMT-P mice there was a significant decrease in tjp1 expression in all three regions of the small intestine; ocln in the ileum; reg3γ in the duodenum and relmβ in both the duodenum and ileum. We also found an increase in colonic mucus layer thickness in mice colonized with FMT-P in contrast with FMT-NP. Finally, our results suggest that gut protozoa, such as Blastocystis hominis, Entamoeba coli, Endolimax nana, Entamoeba histolytica/E. dispar, Iodamoeba bütschlii, and Chilomastix mesnili consortia affect the immunoinflammatory state and induce functional changes in the intestine via the gut microbiota. Likewise, it allows us to establish an FMT model in germ-free mice as a viable alternative to explore the effects that exposure to intestinal parasites could have on the immune response in humans.

Indexed as

Fecal Microbiota TransplantationGerm-Free LifeAnimalsCytokinesDown-RegulationFemaleGastrointestinal MicrobiomeIntestinal MucosaIntestinesMiceMice, Inbred C57BLSpleenT-Lymphocytes, RegulatoryCytokines

Identifiers

PMID39466773
PMCPMC11515975

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.