Evidence map›Paper›PMID 26100020›Full record

ArticleMolecular and cellular biology2015

Salmonella Engages Host MicroRNAs To Modulate SUMOylation: a New Arsenal for Intracellular Survival.

Smriti Verma, Gayatree Mohapatra, Salman Mustfa Ahmad, Sarika Rana, Swati Jain, Jasneet Kaur Khalsa, C V Srikanth

Abstract read
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Article in Molecular and cellular biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

42 citing papers in PubMed.

  1. Review
  2. Gut microbes · 2025
    Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. iScience · 2022
    Article
  16. Article
  17. Emerging role of protein modification in inflammatory bowel disease.Journal of Zhejiang University. Science. B · 2022
    Review
  18. Article
  19. International journal of molecular sciences · 2021
    Article
  20. Review
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

7 authors.

Smriti VermaRegional Centre for Biotechnology, Faridabad, India.
Gayatree MohapatraRegional Centre for Biotechnology, Faridabad, India Manipal University, Karnataka, India.
Salman Mustfa AhmadRegional Centre for Biotechnology, Faridabad, India Manipal University, Karnataka, India.
Sarika RanaRegional Centre for Biotechnology, Faridabad, India.
Swati JainRegional Centre for Biotechnology, Faridabad, India.
Jasneet Kaur KhalsaNational Institute of Immunology, New Delhi, India.
C V SrikanthRegional Centre for Biotechnology, Faridabad, India cvsrikanth@rcb.res.in.

Funding

Wellcome Trust
6 · The paper itself

Abstract

Posttranslational modifications (PTMs) can alter many fundamental properties of a protein. One or combinations of them have been known to regulate the dynamics of many cellular pathways and consequently regulate all vital processes. Understandably, pathogens have evolved sophisticated strategies to subvert these mechanisms to achieve instantaneous control over host functions. Here, we present the first report of modulation by intestinal pathogen Salmonella enterica serovar Typhimurium (S. Typhimurium) of host SUMOylation, a PTM pathway central to all fundamental cellular processes. Both in cell culture and in a mouse model, we observed that S. Typhimurium infection led to a dynamic SUMO-conjugated proteome alteration. The intracellular survival of S. Typhimurium was dependent on SUMO status as revealed by reduced infection and Salmonella-induced filaments (SIFs) in SUMO-upregulated cells. S. Typhimurium-dependent SUMO modulation was seen as a result of depletion of crucial SUMO pathway enzymes Ubc-9 and PIAS1, at both the protein and the transcript levels. Mechanistically, depletion of Ubc-9 relied on upregulation of small noncoding RNAs miR30c and miR30e during S. Typhimurium infection. This was necessary and sufficient for both down-modulation of Ubc-9 and a successful infection. Thus, we demonstrate a novel strategy of pathogen-mediated perturbation of host SUMOylation, an integral mechanism underlying S. Typhimurium infection and intracellular survival.

Indexed as

AnimalsCell Line, TumorFemaleHeLa CellsHost-Pathogen InteractionsHumansMiceMice, Inbred C57BLMicroRNAsProtein Inhibitors of Activated STATSalmonella InfectionsSalmonella typhimuriumSumoylationUbiquitin-Conjugating EnzymesUbiquitin-Conjugating Enzyme UBC9MicroRNAsMirn30d microRNA, mousePias1 protein, mouseProtein Inhibitors of Activated STATUbiquitin-Conjugating EnzymesUbiquitin-Conjugating Enzyme UBC9

Identifiers

PMID26100020
PMCPMC4525320

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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.