Evidence map›Paper›PMID 27590448›Full record

ArticleBMC bioinformatics2016

MMinte: an application for predicting metabolic interactions among the microbial species in a community.

Helena Mendes-Soares, Michael Mundy, Luis Mendes Soares, Nicholas Chia

Open access · goldAbstract read
In one paragraph

Article in BMC bioinformatics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
5.4field-weighted citation impact, top 4% 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

36 citing papers in PubMed, 73 citations in OpenAlex.

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  15. Metabolic modelling approaches for describing and engineering microbial communities.Computational and structural biotechnology journal · 2021
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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

4 authors at 2 institutions in 1 country.

Helena Mendes-SoaresMicrobiome Program, Center for Individualized Medicine, Mayo Clinic, 200 First St. SW, Rochester, 55905, MN, USA. soares.maria@mayo.edu.ORCID http://orcid.org/0000-0002-6727-4327
Michael MundyMicrobiome Program, Center for Individualized Medicine, Mayo Clinic, 200 First St. SW, Rochester, 55905, MN, USA.
Luis Mendes SoaresHarvard Medical School, Boston, MA, USA.
Nicholas ChiaMicrobiome Program, Center for Individualized Medicine, Mayo Clinic, 200 First St. SW, Rochester, 55905, MN, USA. chia.nicholas@mayo.edu.
Mayo Clinic · USHarvard University · US

Funding

Microbial Metabolic Toxicity Drives Colon CancerR01CA179243 · NCI · MAYO CLINIC ROCHESTER · PI CHIA, NICHOLAS · 2014 to 2018
$2.0M
NCI NIH HHS R01 CA179243
6 · The paper itself

Abstract

backgroundThe explosive growth of microbiome research has yielded great quantities of data. These data provide us with many answers, but raise just as many questions. 16S rDNA-the backbone of microbiome analyses-allows us to assess α-diversity, β-diversity, and microbe-microbe associations, which characterize the overall properties of an ecosystem. However, we are still unable to use 16S rDNA data to directly assess the microbe-microbe and microbe-environment interactions that determine the broader ecology of that system. Thus, properties such as competition, cooperation, and nutrient conditions remain insufficiently analyzed. Here, we apply predictive community metabolic models of microbes identified with 16S rDNA data to probe the ecology of microbial communities.

resultsWe developed a methodology for the large-scale assessment of microbial metabolic interactions (MMinte) from 16S rDNA data. MMinte assesses the relative growth rates of interacting pairs of organisms within a community metabolic network and whether that interaction has a positive or negative effect. Moreover, MMinte's simulations take into account the nutritional environment, which plays a strong role in determining the metabolism of individual microbes. We present two case studies that demonstrate the utility of this software. In the first, we show how diet influences the nature of the microbe-microbe interactions. In the second, we use MMinte's modular feature set to better understand how the growth of Desulfovibrio piger is affected by, and affects the growth of, other members in a simplified gut community under metabolic conditions suggested to be determinant for their dynamics.

conclusionBy applying metabolic models to commonly available sequence data, MMinte grants the user insight into the metabolic relationships between microbes, highlighting important features that may relate to ecological stability, susceptibility, and cross-feeding. These relationships are at the foundation of a wide range of ecological questions that impact our ability to understand problems such as microbially-derived toxicity in colon cancer.

Indexed as

MetabolismMicrobiotaSoftwareBacteriaMetabolic Networks and PathwaysModels, BiologicalSpecies Specificity16S rDNAMetabolic network reconstructionMicrobiomeNetworkPredictive community modeling

Identifiers

PMID27590448
PMCPMC5009493
OpenAlexW2507700719

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.