Evidence map›Paper›PMID 42096158›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2026

Conventional, Gnotobiotic, and Humanized Microbiota Mouse Models of C. difficile Infection.

Daniel Erickson, James Collins

Abstract read
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In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 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

2 authors.

Daniel EricksonDepartment of Microbiology & Immunology, University of Louisville, Louisville, KY, USA.
James CollinsDepartment of Microbiology & Immunology, University of Louisville, Louisville, KY, USA. james.collins.1@louisville.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Clostridioides difficile infection (CDI) remains a significant public health challenge, with murine models serving as a cornerstone for investigating host-pathogen interactions, microbiota dynamics, and therapeutic interventions. Although no single mouse model has become the standard, antibiotic-induced disruption of the gut microbiota remains the most common approach to facilitate C. difficile colonization. Here, we describe flexible and reproducible mouse models of CDI that can be adapted to diverse experimental goals, including studies of acute disease, long-term colonization, and microbiota-mediated resistance. This protocol includes detailed guidance on antibiotic pretreatment, C. difficile challenge, clinical monitoring, and microbial enumeration. We also outline procedures for microbial reconstitution in germ-free mice, enabling the study of defined or humanized microbiota. Practical considerations for minimizing environmental contamination and optimizing reproducibility are also discussed.

Indexed as

Clostridioides difficileClostridium InfectionsGastrointestinal MicrobiomeGerm-Free LifeAnimalsAnti-Bacterial AgentsDisease Models, AnimalHost-Pathogen InteractionsHumansMiceAnti-Bacterial AgentsColonizationGerm-freeMouse model

Identifiers

What OpenQuestion holds

Textmetadata
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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.