Evidence map›Paper›PMID 34242364›Full record

ArticlePLoS pathogens2021

ARHGEF26 enhances Salmonella invasion and inflammation in cells and mice.

Jeffrey S Bourgeois, Liuyang Wang, Agustin F Rabino, Jeffrey Everitt, Monica I Alvarez, Sahezeel Awadia, Erika S Wittchen, Rafael Garcia-Mata, Dennis C Ko

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Human variation impactingCell genomics · 2023
    Article
  7. International journal of molecular sciences · 2022
    Review
  8. Article
  9. Tannic Acid InhibitsFrontiers in microbiology · 2021
    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

9 authors at 4 institutions in 1 country.

Jeffrey S BourgeoisDepartment of Molecular Genetics and Microbiology, School of Medicine, Duke University, Durham, North Carolina, United States of America.ORCID 0000-0001-9037-8418
Liuyang WangDepartment of Molecular Genetics and Microbiology, School of Medicine, Duke University, Durham, North Carolina, United States of America.
Agustin F RabinoDepartment of Biological Sciences, University of Toledo, Toledo, Ohio, United States of America.ORCID 0000-0001-7630-6231
Jeffrey EverittDepartment of Pathology, Duke University Medical Center, Durham, North Carolina, United States of America.ORCID 0000-0003-0273-6284
Monica I AlvarezDepartment of Molecular Genetics and Microbiology, School of Medicine, Duke University, Durham, North Carolina, United States of America.
Sahezeel AwadiaDepartment of Biological Sciences, University of Toledo, Toledo, Ohio, United States of America.ORCID 0000-0003-4082-6985
Erika S WittchenDepartment of Cell Biology and Physiology, University of North Carolina, Chapel Hill, North Carolina, United States of America.ORCID 0000-0003-3177-6808
Rafael Garcia-MataDepartment of Biological Sciences, University of Toledo, Toledo, Ohio, United States of America.ORCID 0000-0002-7116-4411
Dennis C KoDepartment of Molecular Genetics and Microbiology, School of Medicine, Duke University, Durham, North Carolina, United States of America.ORCID 0000-0002-0113-5981
Duke University · USUniversity of Toledo · USDuke Medical Center · USUniversity of North Carolina at Chapel Hill · US

Funding

HUMAN GENETIC VARIATION REGULATING SALMONELLA HOST-PATHOGEN INTERACTIONS AND DISEASE SUSCEPTIBILITYR01AI118903 · NIAID · DUKE UNIVERSITY · PI KO, DENNIS CHUN-YONE · 2015 to 2024
$4.2M
Genetics and Genomics Training GrantT32GM136627 · NIGMS · DUKE UNIVERSITY · PI ALLISON E ASHLEY-KOCH · 2020 to 2026
$3.1M
Regulation of epithelial junctions and lumen morphogenesis by the Scribble/SGEF/Dlg1 complexR01GM136826 · NIGMS · UNIVERSITY OF TOLEDO · PI GARCIA-MATA, RAFAEL · 2020 to 2023
$1.5M
Regulation of Salmonella virulence by interspecies methylthioadenosine signalingR21AI144586 · NIAID · DUKE UNIVERSITY · PI KO, DENNIS CHUN-YONE · 2019 to 2020
$428k
Mechanisms of methylthioadenosine signaling during Salmonella infectionF31AI143147 · NIAID · DUKE UNIVERSITY · PI BOURGEOIS, JEFFREY · 2019 to 2021
$105k
NIAID NIH HHS F31 AI143147NIAID NIH HHS R01 AI118903NIAID NIH HHS R21 AI144586NIGMS NIH HHS R01 GM136826NIGMS NIH HHS T32 GM136627
6 · The paper itself

Abstract

Salmonella hijack host machinery in order to invade cells and establish infection. While considerable work has described the role of host proteins in invasion, much less is known regarding how natural variation in these invasion-associated host proteins affects Salmonella pathogenesis. Here we leveraged a candidate cellular GWAS screen to identify natural genetic variation in the ARHGEF26 (Rho Guanine Nucleotide Exchange Factor 26) gene that renders lymphoblastoid cells susceptible to Salmonella Typhi and Typhimurium invasion. Experimental follow-up redefined ARHGEF26's role in Salmonella epithelial cell infection. Specifically, we identified complex serovar-by-host interactions whereby ARHGEF26 stimulation of S. Typhi and S. Typhimurium invasion into host cells varied in magnitude and effector-dependence based on host cell type. While ARHGEF26 regulated SopB- and SopE-mediated S. Typhi (but not S. Typhimurium) infection of HeLa cells, the largest effect of ARHGEF26 was observed with S. Typhimurium in polarized MDCK cells through a SopB- and SopE2-independent mechanism. In both cell types, knockdown of the ARHGEF26-associated protein DLG1 resulted in a similar phenotype and serovar specificity. Importantly, we show that ARHGEF26 plays a critical role in S. Typhimurium pathogenesis by contributing to bacterial burden in the enteric fever murine model, as well as inflammation in the colitis infection model. In the enteric fever model, SopB and SopE2 are required for the effects of Arhgef26 deletion on bacterial burden, and the impact of sopB and sopE2 deletion in turn required ARHGEF26. In contrast, SopB and SopE2 were not required for the impacts of Arhgef26 deletion on colitis. A role for ARHGEF26 on inflammation was also seen in cells, as knockdown reduced IL-8 production in HeLa cells. Together, these data reveal pleiotropic roles for ARHGEF26 during infection and highlight that many of the interactions that occur during infection that are thought to be well understood likely have underappreciated complexity.

Indexed as

AnimalsGenetic Predisposition to DiseaseGuanine Nucleotide Exchange FactorsHeLa CellsHumansInflammationMiceSalmonella InfectionsSalmonella typhiARHGEF26 protein, humanGuanine Nucleotide Exchange Factors

Identifiers

PMID34242364
PMCPMC8294491
OpenAlexW3182767444

What OpenQuestion 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 OpenQuestion graph.