Evidence map›Paper›PMID 42275076›Full record

ArticleThe ISME journal2026

Aggregative chimeric multicellularity in the absence of lethal kin discrimination.

Michael L Weltzer, Pravas C Roy, Jack Govaerts, Daniel Wall

Abstract read
In one paragraph

Article in The ISME journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Michael L WeltzerDepartment of Molecular Biology, University of Wyoming, 1000 E University Avenue, Laramie, WY 82071,  United States.
Pravas C RoyDepartment of Molecular Biology, University of Wyoming, 1000 E University Avenue, Laramie, WY 82071,  United States.
Jack GovaertsDepartment of Molecular Biology, University of Wyoming, 1000 E University Avenue, Laramie, WY 82071,  United States.
Daniel WallDepartment of Molecular Biology, University of Wyoming, 1000 E University Avenue, Laramie, WY 82071,  United States.ORCID 0000-0002-0273-1371

Funding

Self-nonself recognition and multicellularity in myxobacteria: Equipment supplementR35GM140886 · NIGMS · UNIVERSITY OF WYOMING · PI DANIEL WALL · 2021 to 2026
$2.1M
NIGMS NIH HHS R35 GM140886NIH HHS GM140886
6 · The paper itself

Abstract

Aggregative multicellularity is a cooperative strategy used by some microbes. Unlike plant and animal development, which proceeds through clonal expansion from a single progenitor cell, aggregation is susceptible to genetic conflict and cheating, threatening multicellular stability. Myxococcus xanthus and Dictyostelium spp. are soil-dwelling models that form spore-producing fruiting bodies by aggregation upon starvation. Studies of natural M. xanthus fruiting bodies show that this process is confined to clonemates or close relatives, whereas Dictyostelium spp. can form polyclonal fruiting bodies. Here, we examine kin recognition by co-culturing two distantly related M. xanthus strains under vegetative and starvation conditions. We show that strains segregate and antagonize via their type VI secretion systems (T6SS), yielding monoclonal fruiting bodies. In contrast, mixtures of T6SS mutant strains do not antagonize and form chimeric swarms and fruiting bodies with spores from both strains. Nevertheless, within these T6SS mutant swarms and fruiting bodies, strains segregate, thus revealing that nonlethal kin discrimination mechanisms also exist in this species. These findings further suggest that T6SS are a major mediator of lethal kin discrimination between distantly related strains. Thus, lethal kin discrimination ensures homogeneous populations and monoclonal fruiting body development, whereas nonlethal mechanisms play a more subtle and less discriminatory role similar to Dictyostelium spp.

Indexed as

DictyosteliumMyxococcus xanthusMicrobial InteractionsType VI Secretion SystemsType VI Secretion Systemsfruiting body developmentkin discriminationmyxobacteriatype VI secretion system

Identifiers

PMID42275076
PMCPMC13310138

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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.