Evidence map›Paper›PMID 37453420›Full record

ArticleCell host & microbe2023

Discovery of a glutathione utilization pathway in Francisella that shows functional divergence between environmental and pathogenic species.

Yaxi Wang, Hannah E Ledvina, Catherine A Tower, Stanimir Kambarev, Elizabeth Liu, James C Charity, Lieselotte S M Kreuk, Qing Tang, Qiwen Chen, Larry A Gallagher and 13 more

Open access · hybridAbstract read
In one paragraph

Article in Cell host & microbe, 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
1.4field-weighted citation impact, top 19% 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, 9 citations in OpenAlex.

  1. Metabolic engineering ofbioRxiv : the preprint server for biology · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. [Metabolic reprogramming by glutathione S-transferase enhances environmental adaptation ofHua xi kou qiang yi xue za zhi = Huaxi kouqiang yixue zazhi = West China journal of stomatology · 2025
    Article
  6. Article
  7. Review
  8. Diverse roles of low-molecular weight thiol GSH inCurrent research in microbial sciences · 2024
    Article
  9. Review
  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

23 authors at 4 institutions in 1 country.

Yaxi WangDepartment of Microbiology, University of Washington, Seattle, WA 98109, USA.
Hannah E LedvinaDepartment of Microbiology, University of Washington, Seattle, WA 98109, USA.
Catherine A TowerDepartment of Microbiology, University of Washington, Seattle, WA 98109, USA.
Stanimir KambarevPaul G. Allen School for Global Health, Washington State University, Pullman, WA 99164, USA.
Elizabeth LiuDepartment of Microbiology, University of Washington, Seattle, WA 98109, USA.
James C CharityDivision of Infectious Diseases, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Lieselotte S M KreukDepartment of Microbiology, University of Washington, Seattle, WA 98109, USA.
Qing TangDepartment of Microbiology, University of Washington, Seattle, WA 98109, USA.
Qiwen ChenDepartment of Microbiology, University of Washington, Seattle, WA 98109, USA.
Larry A GallagherDepartment of Microbiology, University of Washington, Seattle, WA 98109, USA.
Matthew C RadeyDepartment of Microbiology, University of Washington, Seattle, WA 98109, USA.
Guilhem F RerolleDepartment of Medicine, University of Washington, Seattle, WA 98195, USA.
Yaqiao LiDepartment of Microbiology, University of Washington, Seattle, WA 98109, USA; Institute for Systems Biology, Seattle, WA 98109, USA.
Kelsi M PenewitDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, WA 98195, USA.
Serdar TurkarslanInstitute for Systems Biology, Seattle, WA 98109, USA.
Shawn J SkerrettDepartment of Medicine, University of Washington, Seattle, WA 98195, USA.
Stephen J SalipanteDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, WA 98195, USA.
Nitin S BaligaInstitute for Systems Biology, Seattle, WA 98109, USA.
Joshua J WoodwardDepartment of Microbiology, University of Washington, Seattle, WA 98109, USA.
Simon L DoveDivision of Infectious Diseases, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA.
S Brook PetersonDepartment of Microbiology, University of Washington, Seattle, WA 98109, USA.
Jean CelliPaul G. Allen School for Global Health, Washington State University, Pullman, WA 99164, USA.
Joseph D MougousDepartment of Microbiology, University of Washington, Seattle, WA 98109, USA; Microbial Interactions and Microbiome Center, University of Washington, Seattle, WA 98195, USA; Howard Hughes Medical Institute, University of Washington, Seattle, WA 98109, USA. Electronic address: mougous@uw.edu.
University of Washington · USBoston Children's Hospital · USInstitute for Systems Biology · USWashington State University · US

Funding

Translational Research Center to Expedite Novel Therapies in Cystic FibrosisP30DK089507 · NIDDK · SEATTLE CHILDREN'S HOSPITAL · PI Christopher Hooper Goss · 2010 to 2026
$21.4M
Identity, function and control of Francisella effectors encoded outside its pathogenicity islandR01AI145954 · NIAID · UNIVERSITY OF WASHINGTON · PI DOVE, SIMON L, MOUGOUS, JOSEPH DAVID · 2019 to 2023
$3.7M
NIAID NIH HHS R01 AI145954NIDDK NIH HHS P30 DK089507
6 · The paper itself

Abstract

Glutathione (GSH) is an abundant metabolite within eukaryotic cells that can act as a signal, a nutrient source, or serve in a redox capacity for intracellular bacterial pathogens. For Francisella, GSH is thought to be a critical in vivo source of cysteine; however, the cellular pathways permitting GSH utilization by Francisella differ between strains and have remained poorly understood. Using genetic screening, we discovered a unique pathway for GSH utilization in Francisella. Whereas prior work suggested GSH catabolism initiates in the periplasm, the pathway we define consists of a major facilitator superfamily (MFS) member that transports intact GSH and a previously unrecognized bacterial cytoplasmic enzyme that catalyzes the first step of GSH degradation. Interestingly, we find that the transporter gene for this pathway is pseudogenized in pathogenic Francisella, explaining phenotypic discrepancies in GSH utilization among Francisella spp. and revealing a critical role for GSH in the environmental niche of these bacteria.

Indexed as

FrancisellaFrancisella tularensisAnimalsBacterial ProteinsDNA Transposable ElementsGlutathioneMacrophagesMembrane Transport ProteinsMicePhylogenyTularemiaBacterial ProteinsDNA Transposable ElementsGlutathioneglutathione transporterMembrane Transport Proteins

Identifiers

PMID37453420
PMCPMC10763578
OpenAlexW4384344018

What OpenQuestion holds

Textmetadata
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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.