Evidence map›Paper›PMID 34082713›Full record

ArticleBMC microbiology2021

Lactobacillus rhamnosus GG modifies the metabolome of pathobionts in gnotobiotic mice.

Jinhee Kim, Iyshwarya Balasubramanian, Sheila Bandyopadhyay, Ian Nadler, Rajbir Singh, Danielle Harlan, Amanda Bumber, Yuling He, Lee J Kerkhof, Nan Gao and 2 more

Open access · goldAbstract read
In one paragraph

Article in BMC microbiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

16 citing papers in PubMed, 27 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

12 authors at 3 institutions in 2 countries.

Jinhee Kim *Department of Pharmacology, Physiology and Neurosciences, Medical Science Building, New Jersey Medical School, Rutgers University, Newark, NJ, 07103, USA.
Iyshwarya Balasubramanian *Department of Biological Sciences, Life Science Center, Rutgers University, Newark, NJ, 07102, USA.
Sheila BandyopadhyayDepartment of Biological Sciences, Life Science Center, Rutgers University, Newark, NJ, 07102, USA.
Ian NadlerDepartment of Pharmacology, Physiology and Neurosciences, Medical Science Building, New Jersey Medical School, Rutgers University, Newark, NJ, 07103, USA.
Rajbir SinghDepartment of Biological Sciences, Life Science Center, Rutgers University, Newark, NJ, 07102, USA.
Danielle HarlanDepartment of Pharmacology, Physiology and Neurosciences, Medical Science Building, New Jersey Medical School, Rutgers University, Newark, NJ, 07103, USA.
Amanda BumberComparative Medicine Resources, Rutgers University, Newark, NJ, 07103, USA.
Yuling HeDepartment of Medicine, Clinical Academic Building, Robert Wood Johnson Medical School, Rutgers University, New Brunswick, NJ, 08901, USA.
Lee J KerkhofDepartment of Marine and Coastal Sciences, Rutgers University, 71 Dudley Rd, New Brunswick, NJ, 08901, USA.
Nan GaoDepartment of Biological Sciences, Life Science Center, Rutgers University, Newark, NJ, 07102, USA.
Xiaoyang SuDepartment of Medicine, Clinical Academic Building, Robert Wood Johnson Medical School, Rutgers University, New Brunswick, NJ, 08901, USA.
Ronaldo P FerrarisDepartment of Pharmacology, Physiology and Neurosciences, Medical Science Building, New Jersey Medical School, Rutgers University, Newark, NJ, 07103, USA. ferraris@njms.rutgers.edu.
Rutgers, The State University of New Jersey · USFirst Affiliated Hospital of GuangXi Medical University · CNJohnson University · US

Funding

Research Supplements to Promote Diversity in Health-Related ResearchR01DK119198 · NIDDK · RUTGERS THE STATE UNIV OF NJ NEWARK · PI GAO, NAN, KIELA, PAWEL R · 2019 to 2023
$1.9M
Endosomal Control of Microbe-Host HomeostasisR01DK102934 · NIDDK · RUTGERS THE STATE UNIV OF NJ NEWARK · PI GAO, NAN · 2014 to 2018
$1.8M
Mucosal modulation by LGG and R. gnavus specific tryptophan metabolitesR01AT010243 · NCCIH · RUTGERS THE STATE UNIV OF NJ NEWARK · PI FERRARIS, RONALDO PARAOAN, GAO, NAN · 2018 to 2021
$1.6M
Salmonella-host interaction is mediated by a novel Cdc42 effector and lipidationsF31DK121428 · NIDDK · RUTGERS THE STATE UNIV OF NJ NEWARK · PI BANDYOPADHYAY, SHEILA · 2019 to 2021
$131k
NCCIH NIH HHS R01 AT010243NIDDK NIH HHS F31 DK121428NIDDK NIH HHS R01 DK102934NIDDK NIH HHS R01 DK119198
6 · The paper itself

Abstract

backgroundLactobacillus rhamnosus GG (LGG) is the most widely used probiotic, but the mechanisms underlying its beneficial effects remain unresolved. Previous studies typically inoculated LGG in hosts with established gut microbiota, limiting the understanding of specific impacts of LGG on host due to numerous interactions among LGG, commensal microbes, and the host. There has been a scarcity of studies that used gnotobiotic animals to elucidate LGG-host interaction, in particular for gaining specific insights about how it modifies the metabolome. To evaluate whether LGG affects the metabolite output of pathobionts, we inoculated with LGG gnotobiotic mice containing Propionibacterium acnes, Turicibacter sanguinis, and Staphylococcus aureus (PTS).

results16S rRNA sequencing of fecal samples by Ion Torrent and MinION platforms showed colonization of germ-free mice by PTS or by PTS plus LGG (LTS). Although the body weights and feeding rates of mice remained similar between PTS and LTS groups, co-associating LGG with PTS led to a pronounced reduction in abundance of P. acnes in the gut. Addition of LGG or its secretome inhibited P. acnes growth in culture. After optimizing procedures for fecal metabolite extraction and metabolomic liquid chromatography-mass spectrometry analysis, unsupervised and supervised multivariate analyses revealed a distinct separation among fecal metabolites of PTS, LTS, and germ-free groups. Variables-important-in-projection scores showed that LGG colonization robustly diminished guanine, ornitihine, and sorbitol while significantly elevating acetylated amino acids, ribitol, indolelactic acid, and histamine. In addition, carnitine, betaine, and glutamate increased while thymidine, quinic acid and biotin were reduced in both PTS and LTS groups. Furthermore, LGG association reduced intestinal mucosal expression levels of inflammatory cytokines, such as IL-1α, IL-1β and TNF-α.

conclusionsLGG co-association had a negative impact on colonization of P. acnes, and markedly altered the metabolic output and inflammatory response elicited by pathobionts.

Indexed as

AnimalsBacillotaCytokinesFemaleGastrointestinal MicrobiomeGerm-Free LifeGram-Positive Bacterial InfectionsHumansLacticaseibacillus rhamnosusMaleMiceMice, Inbred C57BLProbioticsPropionibacterium acnesStaphylococcus aureusCytokinesCompetitive exclusionFecal metabolitesGerm-free miceInflammationLiquid chromatography, mass spectrometryMicrobiotaPropionibacterium acnes

Identifiers

PMID34082713
PMCPMC8176599
OpenAlexW3164106843

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.