Evidence map›Paper›PMID 39822045›Full record

ArticleJournal of experimental zoology. Part B, Molecular and developmental evolution2025

High Nutritional Conditions Influence Feeding Plasticity in Pristionchus pacificus and Render Worms Non-Predatory.

Veysi Piskobulu, Marina Athanasouli, Hanh Witte, Christian Feldhaus, Adrian Streit, Ralf J Sommer

Abstract read
In one paragraph

Article in Journal of experimental zoology. Part B, Molecular and developmental evolution, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Developmental transcriptomics inGenome research · 2025
    Article
  4. Article
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

6 authors.

Veysi PiskobuluDepartment for Integrative Evolutionary Biology, Max-Planck Institute for Biology Tübingen, Tübingen, Germany.
Marina AthanasouliDepartment for Integrative Evolutionary Biology, Max-Planck Institute for Biology Tübingen, Tübingen, Germany.
Hanh WitteDepartment for Integrative Evolutionary Biology, Max-Planck Institute for Biology Tübingen, Tübingen, Germany.
Christian FeldhausMax-Planck Institute for Biology Tübingen, BioOptics Facility, Tübingen, Germany.
Adrian StreitDepartment for Integrative Evolutionary Biology, Max-Planck Institute for Biology Tübingen, Tübingen, Germany.
Ralf J SommerDepartment for Integrative Evolutionary Biology, Max-Planck Institute for Biology Tübingen, Tübingen, Germany.ORCID http://orcid.org/0000-0003-1503-7749

Funding

This study was supported by Max-Planck-Gesellschaft.
6 · The paper itself

Abstract

Developmental plasticity, the ability of a genotype to produce different phenotypes in response to environmental conditions, has been subject to intense studies in the last four decades. The self-fertilising nematode Pristionchus pacificus has been developed as a genetic model system for studying developmental plasticity due to its mouth-form polyphenism that results in alternative feeding strategies with a facultative predatory and non-predatory mouth form. Many studies linked molecular aspects of the regulation of mouth-form polyphenism with investigations of its evolutionary and ecological significance. Also, several environmental factors influencing P. pacificus feeding structure expression were identified including temperature, culture condition and population density. However, the nutritional plasticity of the mouth form has never been properly investigated although polyphenisms are known to be influenced by changes in nutritional conditions. For instance, studies in eusocial insects and scarab beetles have provided significant mechanistic insights into the nutritional regulation of polyphenisms but also other forms of plasticity. Here, we study the influence of nutrition on mouth-form polyphenism in P. pacificus through experiments with monosaccharide and fatty acid supplementation. We show that in particular glucose supplementation renders worms non-predatory. Subsequent transcriptomic and mutant analyses indicate that de novo fatty acid synthesis and peroxisomal beta-oxidation pathways play an important role in the mediation of this plastic response. Finally, the analysis of fitness consequences through fecundity counts suggests that non-predatory animals have an advantage over predatory animals grown in the glucose-supplemented condition.

Indexed as

Adaptation, PhysiologicalDietNutritional StatusRhabditidaAnimalsEnvironmentFeeding BehaviorGlucoseMouthOleic AcidPredatory BehaviorSelf-FertilizationGlucoseOleic Aciddevelopmental plasticityfatty acidsglucosenutritionpolyphenismPristionchus pacificus

Identifiers

PMID39822045
PMCPMC11788882

What Socratic holds

Textmetadata
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 Socratic graph.