Evidence map›Paper›PMID 26125937›Full record

ArticlePloS one2015

Identification of Candidate Adherent-Invasive E. coli Signature Transcripts by Genomic/Transcriptomic Analysis.

Yuanhao Zhang, Leahana Rowehl, Julia M Krumsiek, Erika P Orner, Nurmohammad Shaikh, Phillip I Tarr, Erica Sodergren, George M Weinstock, Edgar C Boedeker, Xuejian Xiong and 4 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.2field-weighted citation impact, top 15% 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

23 citing papers in PubMed, 40 citations in OpenAlex.

  1. Journal of bacteriology · 2026
    Review
  2. Decoding the power of the microbiome in human health.Frontiers in cellular and infection microbiology · 2026
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. The Diversity ofMicroorganisms · 2023
    Review
  8. Identification of differences in gene expression implicated in the Adherent-InvasiveFrontiers in cellular and infection microbiology · 2023
    Article
  9. Characterization of Adherent-InvasiveInternational journal of molecular sciences · 2022
    Article
  10. Article
  11. Article
  12. Why the discovery of adherent-invasiveWorld journal of biological chemistry · 2020
    Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 6 institutions in 2 countries.

Yuanhao ZhangDepartment of Applied Mathematics and Statistics, Stony Brook University, Stony Brook, New York, United States of America.
Leahana RowehlDepartment of Medicine, Stony Brook University, Stony Brook, New York, United States of America.
Julia M KrumsiekDepartment of Pediatrics, Stony Brook University, Stony Brook, New York, United States of America.
Erika P OrnerDepartment of Medicine, Stony Brook University, Stony Brook, New York, United States of America.
Nurmohammad ShaikhDepartment of Pediatrics, Washington University St. Louis, St. Louis, Missouri, United States of America.
Phillip I TarrDepartment of Pediatrics, Washington University St. Louis, St. Louis, Missouri, United States of America; Department of Molecular Microbiology, Washington University St. Louis, St. Louis, Missouri, United States of America.
Erica SodergrenThe Genome Institute, Washington University St. Louis, St. Louis, Missouri, United States of America.
George M WeinstockThe Genome Institute, Washington University St. Louis, St. Louis, Missouri, United States of America.
Edgar C BoedekerDepartment of Medicine, University of New Mexico, Albuquerque, New Mexico, United States of America.
Xuejian XiongProgram in Molecular Structure and Function, The Hospital for Sick Children, Toronto, Canada.
John ParkinsonDepartment of Biochemistry & Molecular and Medical Genetics, University of Toronto, Toronto, Canada.
Daniel N FrankDepartment of Medicine, University of Colorado, Denver, Colorado, United States of America.
Ellen LiDepartment of Medicine, Stony Brook University, Stony Brook, New York, United States of America.
Grace GathunguDepartment of Pediatrics, Stony Brook University, Stony Brook, New York, United States of America.
Stony Brook University · USWashington University in St. Louis · USHospital for Sick Children · CAUniversity of Colorado Denver · USUniversity of New Mexico · USUniversity of Toronto · CA

Funding

Washington University DDRCC Supplemental Equipment RequestP30DK052574 · NIDDK · WASHINGTON UNIVERSITY · PI Nicholas O. Davidson · 2000 to 2026
$30.8M
NIDDK NIH HHS 5P30 DK052574
6 · The paper itself

Abstract

Adherent-invasive Escherichia coli (AIEC) strains are detected more frequently within mucosal lesions of patients with Crohn's disease (CD). The AIEC phenotype consists of adherence and invasion of intestinal epithelial cells and survival within macrophages of these bacteria in vitro. Our aim was to identify candidate transcripts that distinguish AIEC from non-invasive E. coli (NIEC) strains and might be useful for rapid and accurate identification of AIEC by culture-independent technology. We performed comparative RNA-Sequence (RNASeq) analysis using AIEC strain LF82 and NIEC strain HS during exponential and stationary growth. Differential expression analysis of coding sequences (CDS) homologous to both strains demonstrated 224 and 241 genes with increased and decreased expression, respectively, in LF82 relative to HS. Transition metal transport and siderophore metabolism related pathway genes were up-regulated, while glycogen metabolic and oxidation-reduction related pathway genes were down-regulated, in LF82. Chemotaxis related transcripts were up-regulated in LF82 during the exponential phase, but flagellum-dependent motility pathway genes were down-regulated in LF82 during the stationary phase. CDS that mapped only to the LF82 genome accounted for 747 genes. We applied an in silico subtractive genomics approach to identify CDS specific to AIEC by incorporating the genomes of 10 other previously phenotyped NIEC. From this analysis, 166 CDS mapped to the LF82 genome and lacked homology to any of the 11 human NIEC strains. We compared these CDS across 13 AIEC, but none were homologous in each. Four LF82 gene loci belonging to clustered regularly interspaced short palindromic repeats region (CRISPR)--CRISPR-associated (Cas) genes were identified in 4 to 6 AIEC and absent from all non-pathogenic bacteria. As previously reported, AIEC strains were enriched for pdu operon genes. One CDS, encoding an excisionase, was shared by 9 AIEC strains. Reverse transcription quantitative polymerase chain reaction assays for 6 genes were conducted on fecal and ileal RNA samples from 22 inflammatory bowel disease (IBD), and 32 patients without IBD (non-IBD). The expression of Cas loci was detected in a higher proportion of CD than non-IBD fecal and ileal RNA samples (p <0.05). These results support a comparative genomic/transcriptomic approach towards identifying candidate AIEC signature transcripts.

Indexed as

Bacterial AdhesionCrohn DiseaseDown-RegulationEscherichia coliEscherichia coli InfectionsGenome, BacterialGenomicsHumansIleumIntestinal MucosaMacrophagesRNA, BacterialSequence Analysis, RNASignal TransductionTranscriptomeUp-RegulationRNA, Bacterial

Identifiers

PMID26125937
PMCPMC4509574
OpenAlexW1538285828

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.