Evidence map›Paper›PMID 24914179›Full record

ArticleJournal of bacteriology2014

Leucine-responsive regulatory protein Lrp and PapI homologues influence phase variation of CS31A fimbriae.

Richard Graveline, Philippe Garneau, Christine Martin, Michaël Mourez, Mark A Hancock, Rémi Lavoie, Josée Harel

Open access · bronzeAbstract read
In one paragraph

Article in Journal of bacteriology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Alanine dehydrogenases in mycobacteria.Journal of microbiology (Seoul, Korea) · 2019
    Review
  5. Article
  6. 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

7 authors at 3 institutions in 2 countries.

Richard GravelineGroupe de Recherche sur les Maladies Infectieuses du Porc (GREMIP) and Centre de Recherche en Infectiologie Porcine (CRIP), Université de Montréal, Saint-Hyacinthe, Quebec, Canada.
Philippe GarneauGroupe de Recherche sur les Maladies Infectieuses du Porc (GREMIP) and Centre de Recherche en Infectiologie Porcine (CRIP), Université de Montréal, Saint-Hyacinthe, Quebec, Canada.
Christine MartinInstitut National de la Recherche Agronomique, Saint-Genès-Champanelle, France.
Michaël MourezGroupe de Recherche sur les Maladies Infectieuses du Porc (GREMIP) and Centre de Recherche en Infectiologie Porcine (CRIP), Université de Montréal, Saint-Hyacinthe, Quebec, Canada.
Mark A HancockMcGill University Surface Plasmon Resonance (SPR) Facility, Montréal, Quebec, Canada.
Rémi LavoieGroupe de Recherche sur les Maladies Infectieuses du Porc (GREMIP) and Centre de Recherche en Infectiologie Porcine (CRIP), Université de Montréal, Saint-Hyacinthe, Quebec, Canada.
Josée HarelGroupe de Recherche sur les Maladies Infectieuses du Porc (GREMIP) and Centre de Recherche en Infectiologie Porcine (CRIP), Université de Montréal, Saint-Hyacinthe, Quebec, Canada josee.harel@umontreal.ca.
Université de Montréal · CAInstitut National de la Recherche Agronomique · MAMcGill University · CA

Funding

Canadian Institutes of Health Research
6 · The paper itself

Abstract

CS31A, a K88-related surface antigen specified by the clp operon, is a member of the type P family of adhesive factors and plays a key role in the establishment of disease caused by septicemic and enterotoxigenic Escherichia coli strains. Its expression is under the control of methylation-dependent transcriptional regulation, for which the leucine-responsive regulatory protein (Lrp) is essential. CS31A is preferentially in the OFF state and exhibits distinct regulatory features compared to the regulation of other P family members. In the present study, surface plasmon resonance and DNase I protection assays showed that Lrp binds to the distal moiety of the clp regulatory region with low micromolar affinity compared to its binding to the proximal moiety, which exhibits stronger, nanomolar affinity. The complex formation was also influenced by the addition of PapI or FooI, which increased the affinity of Lrp for the clp distal and proximal regions and was required to induce phase variation. The influence of PapI or FooI, however, was predominantly associated with a more complete shutdown of clp expression, in contrast to what has previously been observed with AfaF (a PapI ortholog). Taken together, these results suggest that the preferential OFF state observed in CS31A cells is mainly due to the weak interaction of the leucine-responsive regulatory protein with the clp distal region and that the PapI homolog favors the OFF phase. Within the large repertoire of fimbrial variants in the P family, our study illustrates that having a fimbrial operon that lacks its own PapI ortholog allows it to be more flexibly regulated by other orthologs in the cell.

Indexed as

Gene Expression Regulation, BacterialAntigens, BacterialDNA, BacterialDNA FootprintingEscherichia coliEscherichia coli ProteinsLeucine-Responsive Regulatory ProteinPromoter Regions, GeneticProtein BindingRepressor ProteinsSurface Plasmon ResonanceAntigens, BacterialclpG protein, E coliDNA, BacterialEscherichia coli ProteinsLeucine-Responsive Regulatory ProteinLrp protein, E coliPapI protein, E coliRepressor Proteins

Identifiers

PMID24914179
PMCPMC4135631
OpenAlexW2038505618

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.