Evidence map›Paper›PMID 37578251›Full record

ArticleJournal of visualized experiments : JoVE2023

Methodology to Metabolically Inactivate Bacteria for Caenorhabditis elegans Research.

Safa Beydoun, Elizabeth S Kitto, Emily Wang, Shijiao Huang, Scott F Leiser

Open access · greenAbstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.3field-weighted citation impact, top 16% 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

10 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. UtilizingPreventive nutrition and food science · 2026
    Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Chemical Genetics inACS chemical biology · 2024
    Article
  10. 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

5 authors at 1 institution in 1 country.

Safa Beydoun *Molecular and Integrative Physiology Department, University of Michigan, Ann Arbor.
Elizabeth S Kitto *Molecular and Integrative Physiology Department, University of Michigan, Ann Arbor.
Emily WangMolecular and Integrative Physiology Department, University of Michigan, Ann Arbor.
Shijiao HuangMolecular and Integrative Physiology Department, University of Michigan, Ann Arbor.
Scott F LeiserMolecular and Integrative Physiology Department, University of Michigan, Ann Arbor; Department of Internal Medicine, University of Michigan, Ann Arbor; leiser@umich.edu.
University of Michigan–Ann Arbor · US

Funding

Research Training in BiogerontologyT32AG000114 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SCOTT PLETCHER · 1985 to 2026
$12.4M
Flavin-containing monooxygenases in endogenous metabolism and agingR01AG075061 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SCOTT F LEISER · 2022 to 2026
$2.1M
Mechanisms of the cell non-autonomous dietary restriction pathwayR01AG059583 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LEISER, SCOTT F · 2018 to 2022
$1.9M
Novel approaches to study emerging roles of xenobiotic enzymesR21AG059117 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LEISER, SCOTT F · 2018 to 2019
$429k
NIA NIH HHS R01 AG059583NIA NIH HHS R01 AG075061NIA NIH HHS R21 AG059117NIA NIH HHS T32 AG000114
6 · The paper itself

Abstract

Caenorhabditis elegans is a common model organism for research in genetics, development, aging, metabolism, and behavior. Because C. elegans consume a diet of live bacteria, the metabolic activity of their food source can confound experiments looking for the direct effects of various interventions on the worm. To avoid the confounding effects of bacterial metabolism, C. elegans researchers have used multiple methods to metabolically inactivate bacteria, including ultraviolet (UV)-irradiation, heat-killing, and antibiotics. UV treatment is relatively low-throughput and cannot be used in liquid culture because each plate must be examined for successful bacterial killing. A second treatment method, heat-killing, negatively affects the texture and nutritional quality of the bacteria, leading to the developmental arrest of C. elegans. Finally, antibiotic treatment can directly alter C. elegans physiology in addition to preventing bacterial growth. This manuscript describes an alternative method to metabolically inactivate bacteria using paraformaldehyde (PFA). PFA treatment cross-links proteins within bacterial cells to prevent metabolic activity while preserving cellular structure and nutritional content. This method is high-throughput and can be used in liquid culture or solid plates, as testing one plate of PFA-treated bacteria for growth validates the whole batch. Metabolic inactivation through PFA treatment can be used to eliminate the confounding effects of bacterial metabolism on studies of drug or metabolite supplementation, stress resistance, metabolomics, and behavior in C. elegans.

Indexed as

Caenorhabditis elegansEscherichia coliFormaldehydeMicrobiological TechniquesAnimal ExperimentationAnimalsMetabolomicsModels, AnimalPolymersFormaldehydeparaformPolymers

Identifiers

PMID37578251
PMCPMC11064985
OpenAlexW4385332203

What OpenQuestion holds

Textmetadata
LicenceTDM
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.