Evidence map›Paper›PMID 31659191›Full record

ArticleScientific reports2019

Identification of novel targets for host-directed therapeutics against intracellular Staphylococcus aureus.

Natalia Bravo-Santano, Pablo Capilla-Lasheras, Luis M Mateos, Yolanda Calle, Volker Behrends, Michal Letek

Abstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Review
  3. Host-directed microRNA-based intervention against intracellularFrontiers in cellular and infection microbiology · 2026
    Article
  4. Frontiers in bioinformatics · 2026
    Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. 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

6 authors.

Natalia Bravo-SantanoHealth Sciences Research Centre, University of Roehampton, London, UK.ORCID http://orcid.org/0000-0001-9642-6863
Pablo Capilla-LasherasCentre for Ecology and Conservation, University of Exeter, Penryn Campus, Cornwall, UK.
Luis M MateosDepartment of Molecular Biology, Area of Microbiology, University of León, León, Spain.
Yolanda CalleHealth Sciences Research Centre, University of Roehampton, London, UK.
Volker BehrendsHealth Sciences Research Centre, University of Roehampton, London, UK. Volker.Behrends@roehampton.ac.uk.ORCID http://orcid.org/0000-0003-4855-5497
Michal LetekHealth Sciences Research Centre, University of Roehampton, London, UK. Michal.Letek@roehampton.ac.uk.ORCID http://orcid.org/0000-0002-9509-5174

Funding

REGULATION OF CAPILLARY PERFUSION IN MALIGNANT GLIOMASF32CA009122 · NCI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI SHAFFREY, MARK E · 1991 to 1992
–
Biotechnology and Biological Sciences Research Council BB/M009122/1
6 · The paper itself

Abstract

During patient colonization, Staphylococcus aureus is able to invade and proliferate within human cells to evade the immune system and last resort drugs such as vancomycin. Hijacking specific host molecular factors and/or pathways is necessary for pathogens to successfully establish an intracellular infection. In this study, we employed an unbiased shRNA screening coupled with ultra-fast sequencing to screen 16,000 human genes during S. aureus infection and we identified several host genes important for this intracellular pathogen. In addition, we interrogated our screening results to find novel host-targeted therapeutics against intracellular S. aureus. We found that silencing the human gene TRAM2 resulted in a significant reduction of intracellular bacterial load while host cell viability was restored, showing its importance during intracellular infection. Furthermore, TRAM2 is an interactive partner of the endoplasmic reticulum SERCA pumps and treatment with the SERCA-inhibitor Thapsigargin halted intracellular MRSA survival. Our results suggest that Thapsigargin could be repurposed to tackle S. aureus host cell infection in combination with conventional antibiotics.

Indexed as

Drug Delivery SystemsHeLa CellsHumansHuman Umbilical Vein Endothelial CellsMembrane GlycoproteinsMethicillin-Resistant Staphylococcus aureusSarcoplasmic Reticulum Calcium-Transporting ATPasesStaphylococcal InfectionsThapsigarginMembrane GlycoproteinsSarcoplasmic Reticulum Calcium-Transporting ATPasesThapsigarginTRAM2 protein, human

Identifiers

PMID31659191
PMCPMC6817851

What OpenQuestion holds

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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.