Evidence map›Paper›PMID 41243087›Full record

ArticleGut pathogens2025

Murine model of antibiotic-associated Staphylococcus aureus gastrointestinal infections (SAGII) and colonization.

Maria Niamba, Stephanie Yang, Liahm Blank, Liliko Watanabe, Efren Heredia, Ernesto Abel-Santos

Abstract read
In one paragraph

Article in Gut pathogens, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

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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

1 citing paper in PubMed.

  1. 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

6 authors.

Maria NiambaDepartment of Chemistry and Biochemistry, University of Nevada, 4505 Maryland Parkway, Campus Box 4003, Las Vegas, NV, 89154, USA.
Stephanie YangDepartment of Chemistry and Biochemistry, University of Nevada, 4505 Maryland Parkway, Campus Box 4003, Las Vegas, NV, 89154, USA.
Liahm BlankDepartment of Chemistry and Biochemistry, University of Nevada, 4505 Maryland Parkway, Campus Box 4003, Las Vegas, NV, 89154, USA.
Liliko WatanabeDepartment of Chemistry and Biochemistry, University of Nevada, 4505 Maryland Parkway, Campus Box 4003, Las Vegas, NV, 89154, USA.
Efren HerediaDepartment of Chemistry and Biochemistry, University of Nevada, 4505 Maryland Parkway, Campus Box 4003, Las Vegas, NV, 89154, USA.
Ernesto Abel-SantosDepartment of Chemistry and Biochemistry, University of Nevada, 4505 Maryland Parkway, Campus Box 4003, Las Vegas, NV, 89154, USA. ernesto.abelsantos@unlv.edu.

Funding

Effects of estrus cycle stages on murine CDI severityR16AI175022 · NIAID · UNIVERSITY OF NEVADA LAS VEGAS · PI Ernesto V Abel-Santos · 2023 to 2026
$584k
A systems-level approach to probe the effect of a high- fat/high-protein diet in Clostridioides difficile infectionR15AI164346 · NIAID · UNIVERSITY OF NEVADA LAS VEGAS · PI HEDLUND, BRIAN P · 2022 to 2022
$447k
National Institute of Allergy and Infectious Diseases at the National Institute of Health grants numbers R15AI164346, R16AI175022NIAID NIH HHS R15 AI164346NIAID NIH HHS R16 AI175022
6 · The paper itself

Abstract

backgroundStaphylococcus aureus is an opportunistic pathogen that can both colonize the gastrointestinal tract and cause antibiotic associated diarrhea.

methodsTo develop a robust murine model for S. aureus gastrointestinal infection (SAGII) and colonization, mice were (a) treated with varying antibiotic regimes prior to infection, (b) infected with either a methicillin-sensitive S. aureus (MSSA) or a methicillin-resistant S. aureus (MRSA) strain, (c) challenged with different bacterial inocula (d) tested for sexual dimorphism of SAGII virulence, and (e) tested for macronutrient effects on SAGII onset and virulence.

resultsAntibiotic-treated male mice (but not female mice) were highly susceptible to both an MSSA and an MRSA strains. Interestingly, male mice challenged with the laboratory MSSA strain showed more severe and more prolonged SAGII symptomatology than animals challenged with the clinical MRSA strain. Diet composition significantly influenced disease outcome: a high-carbohydrate diet and a high-fat diet led to asymptomatic intestinal colonization followed by delayed SAGII sign onset in male mice. In contrast, a high-protein diet led to an early onset of SAGII signs followed by severe SAGII signs two weeks post-challenge. Furthermore, only the high-protein diet sensitized female mice to SAGII, but their symptomatology remained less severe than in male mice.

conclusionsWe developed a robust murine model for antibiotic-associated S. aureus gastrointestinal infection and colonization. This model shows both sexual dimorphism and macronutrient preference for SAGII signs severity. Diet manipulation can also be used to establish S. aureus colonization of the GI tract. Furthermore, the SAGII murine model demonstrates essential features of S. aureus pathogenesis which could provide understanding about human gastrointestinal colonization and infection mechanisms.

Indexed as

Mice modelMRSAMSSAS. aureus intestinal infection

Identifiers

PMID41243087
PMCPMC12621358

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LicenceCC BY-NC-ND
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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.