Evidence map›Paper›PMID 36279280›Full record

ArticlePLoS neglected tropical diseases2022

The gut microbial metabolic capacity of microbiome-humanized vs. wild type rodents reveals a likely dual role of intestinal bacteria in hepato-intestinal schistosomiasis.

Alba Cortés, John Martin, Bruce A Rosa, Klara A Stark, Simon Clare, Catherine McCarthy, Katherine Harcourt, Cordelia Brandt, Charlotte Tolley, Trevor D Lawley and 4 more

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 16% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. 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

14 authors at 4 institutions in 3 countries.

Alba CortésDepartment of Veterinary Medicine, University of Cambridge, Cambridge, United Kingdom.
John MartinDivision of Infectious Diseases, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, United States of America.
Bruce A RosaDivision of Infectious Diseases, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, United States of America.
Klara A StarkDepartment of Veterinary Medicine, University of Cambridge, Cambridge, United Kingdom.
Simon ClareDepartment of Medicine, University of Cambridge, Cambridge, United Kingdom.
Catherine McCarthyWellcome Trust Sanger Institute, Wellcome Genome Campus, Hinxton, United Kingdom.
Katherine HarcourtWellcome Trust Sanger Institute, Wellcome Genome Campus, Hinxton, United Kingdom.
Cordelia BrandtWellcome Trust Sanger Institute, Wellcome Genome Campus, Hinxton, United Kingdom.
Charlotte TolleyWellcome Trust Sanger Institute, Wellcome Genome Campus, Hinxton, United Kingdom.
Trevor D LawleyWellcome Trust Sanger Institute, Wellcome Genome Campus, Hinxton, United Kingdom.
Makedonka MitrevaDivision of Infectious Diseases, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, United States of America.
Matthew BerrimanWellcome Trust Sanger Institute, Wellcome Genome Campus, Hinxton, United Kingdom.
Gabriel RinaldiWellcome Trust Sanger Institute, Wellcome Genome Campus, Hinxton, United Kingdom.
Cinzia CantacessiDepartment of Veterinary Medicine, University of Cambridge, Cambridge, United Kingdom.ORCID 0000-0001-6863-2950
Wellcome Sanger Institute · GBUniversity of Cambridge · GBWashington University in St. Louis · USUniversitat de València · ES

Funding

Wellcome TrustWellcome Trust 206194
6 · The paper itself

Abstract

Increasing evidence shows that the host gut microbiota might be involved in the immunological cascade that culminates with the formation of tissue granulomas underlying the pathophysiology of hepato-intestinal schistosomiasis. In this study, we investigated the impact of Schistosoma mansoni infection on the gut microbial composition and functional potential of both wild type and microbiome-humanized mice. In spite of substantial differences in microbiome composition at baseline, selected pathways were consistently affected by parasite infection. The gut microbiomes of infected mice of both lines displayed, amongst other features, enhanced capacity for tryptophan and butyrate production, which might be linked to the activation of mechanisms aimed to prevent excessive injuries caused by migrating parasite eggs. Complementing data from previous studies, our findings suggest that the host gut microbiome might play a dual role in the pathophysiology of schistosomiasis, where intestinal bacteria may contribute to egg-associated pathology while, in turn, protect the host from uncontrolled tissue damage.

Indexed as

Gastrointestinal MicrobiomeMicrobiotaSchistosomiasisSchistosomiasis mansoniAnimalsBacteriaMiceRodentia

Identifiers

PMID36279280
PMCPMC9633004
OpenAlexW4307171542

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.