Evidence map›Paper›PMID 24324615›Full record

ArticlePloS one2013

Simultaneous transcriptional profiling of bacteria and their host cells.

Michael S Humphrys, Todd Creasy, Yezhou Sun, Amol C Shetty, Marcus C Chibucos, Elliott F Drabek, Claire M Fraser, Umar Farooq, Naomi Sengamalay, Sandy Ott and 4 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed
6.6field-weighted citation impact, top 3% 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

76 citing papers in PubMed, 137 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Transcriptional profiling ofFrontiers in cellular and infection microbiology · 2025
    Article
  5. Article
  6. Analyzing RNA-Seq Data frombioRxiv : the preprint server for biology · 2024
    Article
  7. Expression activation of over 70% ofInfection and immunity · 2024
    Article
  8. Infection and immunity · 2024
    Article
  9. Review
  10. Article
  11. Frontiers in cellular and infection microbiology · 2023
    Article
  12. Genome organization and genomics inFrontiers in cellular and infection microbiology · 2023
    Review
  13. The role of infected epithelial cells inFrontiers in cellular and infection microbiology · 2023
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review

16 more citing papers are in PubMed but not listed here.

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

14 authors at 1 institution in 1 country.

Michael S HumphrysInstitute for Genome Sciences, University of Maryland School of Medicine, Baltimore, Maryland, United States of America.
Todd Creasy
Yezhou Sun
Amol C Shetty
Marcus C Chibucos
Elliott F Drabek
Claire M Fraser
Umar Farooq
Naomi Sengamalay
Sandy Ott
Huizhong Shou
Patrik M Bavoil
Anup Mahurkar
Garry S A Myers
University of Maryland, Baltimore · US

Funding

Serologic Biomarkers of Human Sexually Transmitted Infection and DiseaseU19AI084044 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI KO, DENNIS CHUN-YONE · 2009 to 2018
$22.8M
NIAID NIH HHS HHSN272200900007CNIAID NIH HHS U19 AI084044NIAID NIH HHS U19AI084044
6 · The paper itself

Abstract

We developed an RNA-Seq-based method to simultaneously capture prokaryotic and eukaryotic expression profiles of cells infected with intracellular bacteria. As proof of principle, this method was applied to Chlamydia trachomatis-infected epithelial cell monolayers in vitro, successfully obtaining transcriptomes of both C. trachomatis and the host cells at 1 and 24 hours post-infection. Chlamydiae are obligate intracellular bacterial pathogens that cause a range of mammalian diseases. In humans chlamydiae are responsible for the most common sexually transmitted bacterial infections and trachoma (infectious blindness). Disease arises by adverse host inflammatory reactions that induce tissue damage & scarring. However, little is known about the mechanisms underlying these outcomes. Chlamydia are genetically intractable as replication outside of the host cell is not yet possible and there are no practical tools for routine genetic manipulation, making genome-scale approaches critical. The early timeframe of infection is poorly understood and the host transcriptional response to chlamydial infection is not well defined. Our simultaneous RNA-Seq method was applied to a simplified in vitro model of chlamydial infection. We discovered a possible chlamydial strategy for early iron acquisition, putative immune dampening effects of chlamydial infection on the host cell, and present a hypothesis for Chlamydia-induced fibrotic scarring through runaway positive feedback loops. In general, simultaneous RNA-Seq helps to reveal the complex interplay between invading bacterial pathogens and their host mammalian cells and is immediately applicable to any bacteria/host cell interaction.

Indexed as

Gene Expression ProfilingMetagenomeTranscriptomeCell Line, TumorChlamydia trachomatisCollagenEpithelial CellsFeedback, PhysiologicalHost-Pathogen InteractionsHumansIntercellular Signaling Peptides and ProteinsSequence Analysis, RNATenascinCollagenGREM1 protein, humanIntercellular Signaling Peptides and ProteinsTenascin

Identifiers

PMID24324615
PMCPMC3851178
OpenAlexW1995896010

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.