Evidence map›Paper›PMID 27353652›Full record

ArticleJournal of bacteriology2016

cis-Encoded Small RNAs, a Conserved Mechanism for Repression of Polysaccharide Utilization in Bacteroides.

Yanlu Cao, Konrad U Förstner, Jörg Vogel, C Jeffrey Smith

Open access · bronzeAbstract read
In one paragraph

Article in Journal of bacteriology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

22 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
  2. Gene regulation inMicrobiology and molecular biology reviews : MMBR · 2025
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Small RNAs Go Global in Human GutJournal of bacteriology · 2021
    Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Receptor uptake arrays for vitamin BEcology and evolution · 2017
    Review
  18. Article
  19. 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

4 authors at 2 institutions in 2 countries.

Yanlu CaoDepartment of Microbiology & Immunology, East Carolina University, Greenville, North Carolina, USA.
Konrad U FörstnerCore Unit Systems Medicine, University of Würzburg, Würzburg, Germany.
Jörg VogelInstitute for Molecular Infection Biology, University of Würzburg, Würzburg, Germany.
C Jeffrey SmithDepartment of Microbiology & Immunology, East Carolina University, Greenville, North Carolina, USA smithcha@ecu.edu.
East Carolina University · USUniversity of Würzburg · DE

Funding

ROLE OF B.FRAGILIS OXYGEN STRESS RESPONSE IN INFECTIONR01AI040588 · NIAID · EAST CAROLINA UNIVERSITY · PI SMITH, CHARLES J. · 1999 to 2014
$3.5M
ROLE OF B.FRAGILIS OXYGEN STRESS RESPONSE IN INFECTIONR56AI040588 · NIAID · EAST CAROLINA UNIVERSITY · PI ROCHA, EDSON R, SMITH, CHARLES J. · 2009 to 2009
$334k
NIAID NIH HHS R01 AI040588NIAID NIH HHS R56 AI040588
6 · The paper itself

Abstract

unlabelledBacteroides is a major component of the human gut microbiota which has a broad impact on the development and physiology of its host and a potential role in a wide range of disease syndromes. The predominance of this genus is due in large part to expansion of paralogous gene clusters, termed polysaccharide utilization loci (PULs), dedicated to the uptake and catabolism of host-derived and dietary polysaccharides. The nutritive value and availability of polysaccharides in the gut vary greatly; thus, their utilization is hierarchical and strictly controlled. A typical PUL includes regulatory genes that induce PUL expression in response to the presence of specific glycan substrates. However, the existence of additional regulatory mechanisms has been predicted to explain phenomena such as hierarchical control and catabolite repression. In this report, a previously unknown layer of regulatory control was discovered in Bacteroides fragilis Exploratory transcriptome sequencing (RNA-seq) analysis revealed the presence of cis-encoded antisense small RNAs (sRNAs) associated with 15 (30%) of the B. fragilis PULs. A model system using the Don (degradation of N-glycans) PUL showed that the donS sRNA negatively regulated Don expression at the transcriptional level, resulting in a decrease in N-glycan utilization. Additional studies performed with other Bacteroides species indicated that this regulatory mechanism is highly conserved and, interestingly, that the regulated PULs appear to be closely linked to the utilization of host-derived glycans rather than dietary plant polysaccharides. The findings described here demonstrate a global control mechanism underlying known PUL regulatory circuits and provide insight into regulation of Bacteroides physiology. IMPORTANCE: The human gut is colonized by a dense microbiota which is essential to the health and normal development of the host. A key to gut homeostasis is the preservation of a stable, diverse microbiota. Bacteroides is a dominant genus in the gut, and the ability of Bacteroides species to efficiently compete for a wide range of glycan energy sources is a crucial advantage for colonization. Glycan utilization is mediated by a large number of polysaccharide utilization loci (PULs) which are regulated by substrate induction. In this report, a novel family of antisense sRNAs is described whose members repress gene expression in a distinct subset of PULs. This repression downregulates PUL expression in the presence of energy sources that are more readily utilized such as glucose, thereby allowing efficient glycan utilization.

Indexed as

BacteroidesDown-RegulationGene Expression Regulation, BacterialPolysaccharidesRNA, BacterialRNA InterferenceRNA, Small InterferingSigma FactorPolysaccharidesRNA, BacterialRNA, Small InterferingSigma Factor

Identifiers

PMID27353652
PMCPMC4999932
OpenAlexW2461179028

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.