Evidence map›Paper›PMID 31611645›Full record

ArticleNature microbiology2019

BioID screen of Salmonella type 3 secreted effectors reveals host factors involved in vacuole positioning and stability during infection.

Vanessa M D'Costa, Etienne Coyaud, Kirsten C Boddy, Estelle M N Laurent, Jonathan St-Germain, Taoyingnan Li, Sergio Grinstein, Brian Raught, John H Brumell

Abstract read
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In one paragraph

Article in Nature microbiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing 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

38 citing papers in PubMed.

  1. Article
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  4. A conserved peptidase governs glucose homeostasis inbioRxiv : the preprint server for biology · 2026
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  9. Proximity biotinylation at the host-bioRxiv : the preprint server for biology · 2025
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  10. Review
  11. The interplay betweenCell insight · 2025
    Review
  12. MappingmBio · 2025
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  15. Functional Divergence of the ParalogInternational journal of molecular sciences · 2024
    Review
  16. Microbiology spectrum · 2024
    Article
  17. mBio · 2023
    Article
  18. Article
  19. Article
  20. 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.

Vanessa M D'CostaCell Biology Program, Hospital for Sick Children, Toronto, Ontario, Canada. vdcosta@uottawa.ca.ORCID http://orcid.org/0000-0003-4340-7778
Etienne CoyaudPrincess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.
Kirsten C BoddyCell Biology Program, Hospital for Sick Children, Toronto, Ontario, Canada.
Estelle M N LaurentPrincess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.
Jonathan St-GermainPrincess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.
Taoyingnan LiCell Biology Program, Hospital for Sick Children, Toronto, Ontario, Canada.
Sergio GrinsteinCell Biology Program, Hospital for Sick Children, Toronto, Ontario, Canada.ORCID http://orcid.org/0000-0002-0795-4160
Brian Raught *Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.
John H Brumell *Cell Biology Program, Hospital for Sick Children, Toronto, Ontario, Canada. john.brumell@sickkids.ca.ORCID http://orcid.org/0000-0002-5802-7789

Funding

CIHR 119289CIHR 143202CIHR 154329
6 · The paper itself

Abstract

Many bacterial pathogens express virulence proteins that are translocated into host cells (herein referred to as effectors), where they can interact with target proteins to manipulate host cell processes. These effector-host protein interactions are often dynamic and transient in nature, making them difficult to identify using traditional interaction-based methods. Here, we performed a systematic comparison between proximity-dependent biotin labelling (BioID) and immunoprecipitation coupled with mass spectrometry to investigate a series of Salmonella type 3 secreted effectors that manipulate host intracellular trafficking (SifA, PipB2, SseF, SseG and SopD2). Using BioID, we identified 632 candidate interactions with 381 unique human proteins, collectively enriched for roles in vesicular trafficking, cytoskeleton components and transport activities. From the subset of proteins exclusively identified by BioID, we report that SifA interacts with BLOC-2, a protein complex that regulates dynein motor activity. We demonstrate that the BLOC-2 complex is necessary for SifA-mediated positioning of Salmonella-containing vacuoles, and affects stability of the vacuoles during infection. Our study provides insight into the coordinated activities of Salmonella type 3 secreted effectors and demonstrates the utility of BioID as a powerful, complementary tool to characterize effector-host protein interactions.

Indexed as

Bacterial ProteinsBiotinGene Knockdown TechniquesHEK293 CellsHeLa CellsHost-Pathogen InteractionsHumansIntracellular Signaling Peptides and ProteinsProtein TransportSalmonellaSalmonella InfectionsSalmonella typhimuriumStaining and LabelingVacuolesBacterial ProteinsBiotinHPS3 protein, humanIntracellular Signaling Peptides and ProteinsSifA protein, Salmonella

Identifiers

What OpenQuestion holds

Textmetadata
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.