Evidence map›Paper›PMID 41529073›Full record

ArticlePLoS computational biology2026

Novel artificial selection method improves function of simulated microbial communities.

Björn Vessman, Pablo Guridi-Fernández, Flor Inés Arias-Sánchez, Sara Mitri

Abstract read
In one paragraph

Article in PLoS computational biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

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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.

Björn VessmanDepartment of Fundamental Microbiology, University of Lausanne, Lausanne, Switzerland.
Pablo Guridi-FernándezDepartment of Fundamental Microbiology, University of Lausanne, Lausanne, Switzerland.
Flor Inés Arias-SánchezBIH Center for Regenerative Therapies (BCRT), Charité - Universitätsmedizin Berlin, Berlin, Germany.
Sara MitriDepartment of Fundamental Microbiology, University of Lausanne, Lausanne, Switzerland.ORCID https://orcid.org/0000-0003-3930-5357

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is increasing interest in artificially selecting or breeding microbial communities, but experiments have reported modest success. Here, we develop computational models to simulate two previously known selection methods and compare them to a new "disassembly" method. We evaluate all three methods in their ability to find a community that could efficiently degrade toxins, whereby investment into degradation results in slower growth. Our disassembly method relies on repeatedly competing different communities of known species combinations against one another, while regularly shuffling around their species combinations. This approach allows many species combinations to be explored, thereby maintaining enough between-community diversity for selection to act on, and resulting in communities with high performance. Nevertheless, selection at the community level in our simulations did not counteract selection at the individual level, nor the communities' ecological dynamics. Species in our model evolved to invest less into community function and more into growth, but increased growth compensated for reduced investment, such that overall community performance was barely affected by within-species evolution. Within-community ecological dynamics were more of a challenge, as we could control them during the selection process, but community composition and function dropped in the longer term. Our work shows that the strength of disassembly lies mainly in its ability to explore different species combinations, and helps to propose alternative designs for community selection experiments.

Indexed as

MicrobiotaModels, BiologicalSelection, GeneticComputational BiologyComputer Simulation

Identifiers

PMID41529073
PMCPMC12829962

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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.