Evidence map›Paper›PMID 19878715›Full record

ArticleMicrobial pathogenesis2010

Development of a live oral attaching and effacing Escherichia coli vaccine candidate using Vibrio cholerae CVD 103-HgR as antigen vector.

Rogeria Keller, Tamara D Hilton, Hernam Rios, Edgar C Boedeker, James B Kaper

Abstract read
In one paragraph

Article in Microbial pathogenesis, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

5 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Review
  3. Live bacterial vaccine vectors: an overview.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2014
    Review
  4. Progress inFrontiers in biology · 2013
    Article
  5. 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

5 authors at 3 institutions in 1 country.

Rogeria KellerCenter for Vaccine Development and Department of Microbiology & Immunology, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Tamara D Hilton
Hernam Rios
Edgar C Boedeker
James B Kaper
University of Maryland, Baltimore · USStanford University · USUniversity of New Mexico · US

Funding

Vaccine strategy for broad spectrum protection agains non-typhoidal salmonellU54AI057168 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI LEVINE, MYRON MAX · 2003 to 2013
$91.5M
DEVELOPMENT OF A LIVE ORAL CHOLERA VACCINER01AI019716 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI KAPER, JAMES B · 1989 to 2010
$4.4M
NOVEL E. COLI 0157:H7 INTESTINAL COLONIZATION FACTORSR01DK058957 · NIDDK · UNIVERSITY OF MARYLAND BALTIMORE · PI KAPER, JAMES B · 2000 to 2009
$3.1M
Intervention strategies of hemorrhagic colitis and HUSR01DK059012 · NIDDK · UNIVERSITY OF NEW MEXICO · PI BOEDEKER, EDGAR C. · 2001 to 2004
$1.1M
DEVELOPMENT OF A LIVE ORAL CHOLERA VACCINER22AI019716 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI KAPER, JAMES B · 1985 to 1991
–
NIAID NIH HHS AI19716NIAID NIH HHS R01 AI019716NIAID NIH HHS U54 AI057168NIAID NIH HHS U54 AI57168NIDDK NIH HHS DK 059012NIDDK NIH HHS DK58957NIDDK NIH HHS R01 DK058957NIDDK NIH HHS R01 DK059012
6 · The paper itself

Abstract

Attaching and effacing Escherichia coli (AEEC) share the ability to induce pedestal formation and intimate adherence of the bacteria to the intestinal epithelial cell and effacement of microvilli of epithelial tissue. The Locus of Enterocyte Effacement (LEE) pathogenicity island encodes the ability to induce attaching and effacing (A/E) lesions and contains the gene eae, which encodes intimin, an outer membrane protein that is an adhesin for A/E lesion formation. Here we show the utility of using intimin as a vaccine to protect rabbits from challenge with rabbit Enteropathogenic E. coli (REPEC), a member of the AEEC family. The C-terminal portion of intimin was delivered by the attenuated Vibrio cholerae vaccine strain CVD 103-HgR. To export intimin, a fusion was engineered with ClyA, a secreted protein from Salmonella enterica serovar Typhi. After immunization, antibodies specific to intimin from serum and bile samples were detected and moderate protection against challenge with a virulent REPEC strain was observed. Compared to animals immunized with vector alone, intimin-immunized rabbits exhibited reduced fecal bacterial shedding, milder diarrheal symptoms, lower weight loss, and reduced colonization of REPEC in the cecum. V. cholerae CVD 103-HgR shows promise as a vector to deliver antigens and confer protection against AEEC pathogens.

Indexed as

Genetic VectorsAdhesins, BacterialAnimalsAntibodies, BacterialAntigens, BacterialBacterial SheddingBileCholera VaccinesColony Count, MicrobialDisease Models, AnimalEscherichia coli InfectionsEscherichia coli ProteinsEscherichia coli VaccinesFecesHumansIleumAdhesins, BacterialAntibodies, BacterialAntigens, Bacterialcholera vaccine CVD 103-HgRCholera VaccineseaeA protein, E coliEscherichia coli ProteinsEscherichia coli VaccinesVaccines, Attenuated

Identifiers

PMID19878715
PMCPMC2814881
OpenAlexW2039006787

What OpenQuestion holds

Textmetadata
LicenceTDM
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.