Evidence map›Paper›PMID 34839237›Full record

ReviewCurrent opinion in microbiology2022

Computational approaches to understanding Clostridioides difficile metabolism and virulence.

Matthew L Jenior, Jason A Papin

Open access · greenAbstract readReview
In one paragraph

Review in Current opinion in microbiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.1field-weighted citation impact, top 49% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

2 authors at 1 institution in 1 country.

Matthew L JeniorDepartment of Biomedical Engineering, University of Virginia, MR-5 2041a, Box 800759, Health System, Charlottesville, VA 22908 USA. Electronic address: mljenior@virginia.edu.
Jason A PapinDepartment of Biomedical Engineering, University of Virginia, MR-5 2041a, Box 800759, Health System, Charlottesville, VA 22908 USA; Department of Medicine, Division of Infectious Diseases & International Health, University of Virginia, Charlottesville, VA, USA; Department of Biochemistry & Molecular Genetics, University of Virginia, Charlottesville, VA, USA. Electronic address: papin@virginia.edu.
University of Virginia Health System · US

Funding

Multi-scale model of microbial phenotype modulation by mucinsR01AI154242 · NIAID · UNIVERSITY OF VIRGINIA · PI FORD, ROSEANNE, PAPIN, JASON · 2020 to 2024
$3.1M
Systems biology of microbe-mediated glucosinolate bioconversion in inflammatory bowel diseaseR01AT010253 · NCCIH · UNIVERSITY OF VIRGINIA · PI PAPIN, JASON · 2018 to 2021
$2.0M
Interdisciplinary Training in Systems & Biomolecular Data ScienceT32GM145443 · NIGMS · UNIVERSITY OF VIRGINIA · PI Kevin A Janes, Jason Papin · 2022 to 2026
$1.5M
NCCIH NIH HHS R01 AT010253NIAID NIH HHS R01 AI154242NIGMS NIH HHS T32 GM145443
6 · The paper itself

Abstract

The progress of infection by Clostridioides difficile is strongly influenced by metabolic cues it encounters as it colonizes the gastrointestinal tract. Both colonization and regulation of virulence have a multi-factorial interaction between host, microbiome, and gene expression cascades. While these connections with metabolism have been understood for some time, many mechanisms of control have remained difficult to directly assay due to high metabolic variability among C. difficile isolates and difficult genetic systems. Computational systems offer a means to interrogate structure of complex or noisy datasets and generate useful, tractable hypotheses to be tested in the laboratory. Recently, in silico techniques have provided powerful insights into metabolic elements of C. difficile infection ranging from virulence regulation to interactions with the gut microbiota. In this review, we introduce and provide context to the methods of computational modeling that have been applied to C. difficile metabolism and virulence thus far. The techniques discussed here have laid the foundation for future multi-scale efforts aimed at understanding the complex interplay of metabolic activity between pathogen, host, and surrounding microbial community in the regulation of C. difficile pathogenesis.

Indexed as

Clostridioides difficileClostridium InfectionsGastrointestinal MicrobiomeClostridioidesHumansVirulence

Identifiers

PMID34839237
PMCPMC8792252
OpenAlexW3217105162

What OpenQuestion holds

Textmetadata
LicenceTDM
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.