Evidence map›Paper›PMID 24810289›Full record

ArticlePloS one2014

Expanding the RpoS/σS-network by RNA sequencing and identification of σS-controlled small RNAs in Salmonella.

Corinne Lévi-Meyrueis, Véronique Monteil, Odile Sismeiro, Marie-Agnès Dillies, Marc Monot, Bernd Jagla, Jean-Yves Coppée, Bruno Dupuy, Françoise Norel

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

33 citing papers in PubMed, 57 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
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  7. Article
  8. Article
  9. RpoS contributes in a host-dependent manner toFrontiers in microbiology · 2022
    Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. σFrontiers in microbiology · 2021
    Article
  17. Article
  18. RpoS-regulatedVirulence · 2020
    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 at 3 institutions in 1 country.

Corinne Lévi-MeyrueisInstitut Pasteur, Unité de Génétique Moléculaire, Département de Microbiologie, Paris, France; CNRS, ERL3526, Paris, France; Université Paris Sud XI, Orsay, France.
Véronique MonteilInstitut Pasteur, Unité de Génétique Moléculaire, Département de Microbiologie, Paris, France; CNRS, ERL3526, Paris, France.
Odile SismeiroInstitut Pasteur, Plate-forme Transcriptome et Epigénome, Département Génomes et génétique, Paris, France.
Marie-Agnès DilliesInstitut Pasteur, Plate-forme Transcriptome et Epigénome, Département Génomes et génétique, Paris, France.
Marc MonotInstitut Pasteur, Laboratoire Pathogenèse des bactéries anaérobies, Département de Microbiologie, Paris, France.
Bernd JaglaInstitut Pasteur, Plate-forme Transcriptome et Epigénome, Département Génomes et génétique, Paris, France.
Jean-Yves CoppéeInstitut Pasteur, Plate-forme Transcriptome et Epigénome, Département Génomes et génétique, Paris, France.
Bruno DupuyInstitut Pasteur, Laboratoire Pathogenèse des bactéries anaérobies, Département de Microbiologie, Paris, France.
Françoise NorelInstitut Pasteur, Unité de Génétique Moléculaire, Département de Microbiologie, Paris, France; CNRS, ERL3526, Paris, France.
Institut Pasteur · FRCentre National de la Recherche Scientifique · FRUniversité Paris-Sud · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The RpoS/σS sigma subunit of RNA polymerase (RNAP) controls a global adaptive response that allows many Gram-negative bacteria to survive starvation and various stresses. σS also contributes to biofilm formation and virulence of the food-borne pathogen Salmonella enterica serovar Typhimurium (S. Typhimurium). In this study, we used directional RNA-sequencing and complementary assays to explore the σS-dependent transcriptome of S. Typhimurium during late stationary phase in rich medium. This study confirms the large regulatory scope of σS and provides insights into the physiological functions of σS in Salmonella. Extensive regulation by σS of genes involved in metabolism and membrane composition, and down-regulation of the respiratory chain functions, were important features of the σS effects on gene transcription that might confer fitness advantages to bacterial cells and/or populations under starving conditions. As an example, we show that arginine catabolism confers a competitive fitness advantage in stationary phase. This study also provides a firm basis for future studies to address molecular mechanisms of indirect regulation of gene expression by σS. Importantly, the σS-controlled downstream network includes small RNAs that might endow σS with post-transcriptional regulatory functions. Of these, four (RyhB-1/RyhB-2, SdsR, SraL) were known to be controlled by σS and deletion of the sdsR locus had a competitive fitness cost in stationary phase. The σS-dependent control of seven additional sRNAs was confirmed in Northern experiments. These findings will inspire future studies to investigate molecular mechanisms and the physiological impact of post-transcriptional regulation by σS.

Indexed as

Sequence Analysis, RNAGene Expression ProfilingGenetic LociRNA, BacterialRNA, Small UntranslatedSalmonella typhimuriumSigma FactorRNA, BacterialRNA, Small UntranslatedSigma Factor

Identifiers

PMID24810289
PMCPMC4014581
OpenAlexW1987191095

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.