Evidence map›Paper›PMID 37762089›Full record

ArticleInternational journal of molecular sciences2023

Probiotics Modulate Host Immune Response and Interact with the Gut Microbiota: Shaping Their Composition and Mediating Antibiotic Resistance.

Walaa K Mousa, Sara Mousa, Rose Ghemrawi, Dana Obaid, Muhammad Sarfraz, Fadia Chehadeh, Shannon Husband

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

19 citing papers in PubMed, 23 citations in OpenAlex.

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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

7 authors at 4 institutions in 3 countries.

Walaa K MousaCollege of Pharmacy, Al Ain University, Abu Dhabi P.O. Box 64141, United Arab Emirates.
Sara MousaCollege of Pharmacy, Al Ain University, Abu Dhabi P.O. Box 64141, United Arab Emirates.
Rose GhemrawiCollege of Pharmacy, Al Ain University, Abu Dhabi P.O. Box 64141, United Arab Emirates.ORCID 0000-0002-2465-0812
Dana ObaidCollege of Pharmacy, Al Ain University, Abu Dhabi P.O. Box 64141, United Arab Emirates.
Muhammad SarfrazCollege of Pharmacy, Al Ain University, Abu Dhabi P.O. Box 64141, United Arab Emirates.ORCID 0000-0002-0516-4966
Fadia ChehadehAnschutz Medical Campus, Colorado School of Public Health, University of Colorado, Aurora, CO 173364, USA.
Shannon HusbandDepartment of Biology, Whitman College, Walla Walla, WA 99362, USA.
Al Ain University · AEColorado School of Public Health · USMansoura University · EGWhitman College · US

Funding

Al Ain University of Science and Technology Ph2022-3-100
6 · The paper itself

Abstract

The consortium of microbes inhabiting the human body, together with their encoded genes and secreted metabolites, is referred to as the "human microbiome." Several studies have established a link between the composition of the microbiome and its impact on human health. This impact spans local gastrointestinal inflammation to systemic autoimmune disorders and neurodegenerative diseases such as Alzheimer's and Autism. Some of these links have been validated by rigorous experiments that identify specific strains as mediators or drivers of a particular condition. Consequently, the development of probiotics to compensate for a missing beneficial microbe(s) has advanced and become popular, especially in the treatment of irritable bowel diseases and to restore disrupted gut flora after antibiotic administration. The widespread use of probiotics is often advocated as a natural ecological therapy. However, this perception is not always accurate, as there is a potential for unexpected interactions when administering live microbial cultures. Here, we designed this research to explore the intricate interactions among probiotics, the host, and microbes through a series of experiments. Our objectives included assessing their immunomodulatory effects, response to oral medications, impact on microbial population dynamics, and mediation of antibiotic resistance. To achieve these goals, we employed diverse experimental protocols, including cell-based enzyme -linked immunosorbent assay (ELISA), antibiotic susceptibility testing, antimicrobial activity assays, computational prediction of probiotic genes responsible for antibiotic resistance, polymerase chain reaction (PCR)-based validation of predicted genes, and survival assays of probiotics in the presence of selected oral medications. Our findings highlight that more than half of the tested probiotics trigger an inflammatory response in the Caco-2 cell line, are influenced by oral medications, exhibit antibacterial activity, and possess genes encoding antimicrobial resistance. These results underscore the necessity for a reevaluation of probiotic usage and emphasize the importance of establishing regulations to govern probiotic testing, approval, and administration.

Indexed as

Gastrointestinal MicrobiomeAnti-Bacterial AgentsCaco-2 CellsDrug Resistance, MicrobialHumansImmunityAnti-Bacterial Agentsantibioticsimmune reactionsinflammationmicrobiomeprobioticsresistance

Identifiers

PMID37762089
PMCPMC10531388
OpenAlexW4386525970

What OpenQuestion holds

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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.