Evidence map›Paper›PMID 24116144›Full record

ArticlePloS one2013

Conditional gene expression in Chlamydia trachomatis using the tet system.

Jason Wickstrum, Lindsay R Sammons, Keasha N Restivo, P Scott Hefty

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 81 papers.

0numbers the graph read from it
0cells of the map it votes in
81citing papers in PubMed
7.6field-weighted citation impact, top 2% 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

81 citing papers in PubMed, 94 citations in OpenAlex.

  1. Article
  2. Conditional dCas12-Mediated Gene Knockdown and Complementation in Chlamydia.Methods in molecular biology (Clifton, N.J.) · 2027
    Article
  3. Article
  4. Review
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  6. Article
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  11. Review
  12. Article
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  14. Type III Secretion inMicrobiology and molecular biology reviews : MMBR · 2023
    Review
  15. Requirement of GrgA forbioRxiv : the preprint server for biology · 2023
    Article
  16. Article
  17. Article
  18. Advances in genetic manipulation ofFrontiers in immunology · 2023
    Review
  19. Review
  20. Article

21 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

4 authors at 1 institution in 1 country.

Jason WickstrumDepartment of Molecular Biosciences, University of Kansas, Lawrence, Kansas, United States of America.
Lindsay R Sammons
Keasha N Restivo
P Scott Hefty
University of Kansas · US

Funding

Development and Validation of Conditional Gene Expression Systems in ChlamydiaR21AI103711 · NIAID · UNIVERSITY OF KANSAS LAWRENCE · PI HEFTY, P SCOTT · 2013 to 2014
$403k
NIAID NIH HHS AI103711NIAID NIH HHS R21 AI103711
6 · The paper itself

Abstract

Chlamydia trachomatis is maintained through a complex bi-phasic developmental cycle that incorporates numerous processes that are poorly understood. This is reflective of the previous paucity of genetic tools available. The recent advent of a method for transforming Chlamydia has enabled the development of essential molecular tools to better study these medically important bacteria. Critical for the study of Chlamydia biology and pathogenesis, is a system for tightly controlled inducible gene expression. To accomplish this, a new shuttle vector was generated with gene expression controlled by the Tetracycline repressor and anhydryotetracycline. Evaluation of GFP expression by this system demonstrated tightly controlled gene regulation with rapid protein expression upon induction and restoration of transcription repression following inducer removal. Additionally, induction of expression could be detected relatively early during the developmental cycle and concomitant with conversion into the metabolically active form of Chlamydia. Uniform and strong GFP induction was observed during middle stages of the developmental cycle. Interestingly, variable induced GFP expression by individual organisms within shared inclusions during later stages of development suggesting metabolic diversity is affecting induction and/or expression. These observations support the strong potential of this molecular tool to enable numerous experimental analyses for a better understanding of the biology and pathogenesis of Chlamydia.

Indexed as

AnimalsAntiportersBacterial ProteinsCell Line, TumorChlamydia trachomatisDose-Response Relationship, DrugGene Expression Regulation, BacterialGenetic VectorsGreen Fluorescent ProteinsMiceMicroscopy, FluorescencePromoter Regions, GeneticRepressor ProteinsReverse Transcriptase Polymerase Chain ReactionTetracycline ResistanceTetracyclines4-epianhydrotetracyclineAntiportersBacterial ProteinsGreen Fluorescent ProteinsRepressor ProteinstetA protein, Bacteriatetracycline resistance-encoding transposon repressor proteinTetracyclines

Identifiers

PMID24116144
PMCPMC3792055
OpenAlexW2156718046

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.