Evidence map›Paper›PMID 11443077›Full record

ArticleJournal of bacteriology2001

Novel topology of BfpE, a cytoplasmic membrane protein required for type IV fimbrial biogenesis in enteropathogenic Escherichia coli.

T E Blank, M S Donnenberg

Open access · greenAbstract read
In one paragraph

Article in Journal of bacteriology, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

25 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
  2. Type IV pili ofEcoSal Plus · 2024
    Review
  3. Article
  4. Article
  5. Article
  6. Editorial.FEMS microbiology reviews · 2015
    Article
  7. Review
  8. Article
  9. Type IV pili in Gram-positive bacteria.Microbiology and molecular biology reviews : MMBR · 2013
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Type IV pili: paradoxes in form and function.Current opinion in structural biology · 2008
    Review
  18. 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

2 authors at 1 institution in 1 country.

T E BlankDivision of Infectious Diseases, Department of Medicine, University of Maryland School of Medicine, 10 South Pine Street, Baltimore, MD 21201, USA.
M S Donnenberg
University of Maryland, Baltimore · US

Funding

MOLECULAR BASIS OF LOCALIZED ADHERENCE IN E. COLIR01AI037606 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI DONNENBERG, MICHAEL S · 1995 to 2009
$2.5M
BFPE STRUCTURE/FUNCTION IN TYPE IV PILUS BIOGENESISF32AI010191 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI BLANK, ERIC T · 1998 to 2000
$39k
NIAID NIH HHS F32 AI010191NIAID NIH HHS F32 AI-10191NIAID NIH HHS R01 AI037606NIAID NIH HHS R01 AI-37606
6 · The paper itself

Abstract

Enteropathogenic Escherichia coli (EPEC) produces the bundle-forming pilus (BFP), a type IV fimbria that has been implicated in virulence, autoaggregation, and localized adherence to epithelial cells. The bfpE gene is one of a cluster of bfp genes previously shown to encode functions that direct BFP biosynthesis. Here, we show that an EPEC strain carrying a nonpolar mutation in bfpE fails to autoaggregate, adhere to HEp-2 cells, or form BFP, thereby demonstrating that BfpE is required for BFP biogenesis. BfpE is a cytoplasmic membrane protein of the GspF family. To determine the membrane topology of BfpE, we fused bfpE derivatives containing 3' truncations and/or internal deletions to alkaline phosphatase and/or beta-galactosidase reporter genes, whose products are active only when localized to the periplasm or cytoplasm, respectively. In addition, we constructed BfpE sandwich fusions using a dual alkaline phosphatase/beta-galactosidase reporter cassette and analyzed BfpE deletion derivatives by sucrose density flotation gradient fractionation. The data from these analyses support a topology in which BfpE contains four hydrophobic transmembrane (TM) segments, a large cytoplasmic segment at its N terminus, and a large periplasmic segment near its C terminus. This topology is dramatically different from that of OutF, another member of the GspF family, which has three TM segments and is predominantly cytoplasmic. These findings provide a structural basis for predicting protein-protein interactions required for assembly of the BFP biogenesis machinery.

Indexed as

Escherichia coli ProteinsAlkaline PhosphataseAmino Acid SequenceBacterial Proteinsbeta-GalactosidaseCyclin-Dependent KinasesEscherichia coliFimbriae, BacterialGene ExpressionGenes, ReporterLac OperonMembrane ProteinsMolecular Sequence DataMutagenesisPhenotypeRecombinant Fusion ProteinsAlkaline PhosphataseBacterial Proteinsbeta-GalactosidaseBfpE protein, E coliCyclin-Dependent KinasesEscherichia coli ProteinsMembrane ProteinsphoA protein, E coliRecombinant Fusion Proteins

Identifiers

PMID11443077
PMCPMC95337
OpenAlexW2102720719

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.