Evidence map›Paper›PMID 29390129›Full record

ArticlePathogens and disease2018

Direct visualization of the expression and localization of chlamydial effector proteins within infected host cells.

Xiaogang Wang, Kevin Hybiske, Richard S Stephens

Open access · bronzeAbstract read
In one paragraph

Article in Pathogens and disease, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

19 citing papers in PubMed, 28 citations in OpenAlex.

  1. Split-GFP Reporter-Based Detection of Chlamydia trachomatis Inclusion Damage.Methods in molecular biology (Clifton, N.J.) · 2027
    Article
  2. Review
  3. Article
  4. Article
  5. Experimental Approaches to Visualize Effector Protein Translocation During Host-Pathogen Interactions.BioEssays : news and reviews in molecular, cellular and developmental biology · 2025
    Review
  6. Article
  7. Article
  8. ThemBio · 2023
    Article
  9. Article
  10. TheInfection and immunity · 2022
    Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. The multiple functions of the numerousMicrobial cell (Graz, Austria) · 2019
    Review
  17. Article
  18. A renewed tool kit to exploreF1000Research · 2019
    Review
  19. 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

3 authors at 2 institutions in 1 country.

Xiaogang WangProgram in Infectious Diseases, School of Public Health, University of California, 51 Koshland Hall, Berkeley, CA 94720, USA.
Kevin HybiskeDivision of Allergy and Infectious Diseases, Department of Medicine, University of Washington, 750 Republican St Seattle, WA 98109, USA.
Richard S StephensProgram in Infectious Diseases, School of Public Health, University of California, 51 Koshland Hall, Berkeley, CA 94720, USA.
University of California, Berkeley · USUniversity of Washington · US

Funding

Mechanisms of Host Cell Infection by ChlamydiaR01AI091851 · NIAID · UNIVERSITY OF CALIFORNIA BERKELEY · PI STEPHENS, RICHARD S · 2011 to 2015
$1.9M
NIAID NIH HHS R01 AI091851NIH HHS AI091851
6 · The paper itself

Abstract

Chlamydia secrete into host cells a diverse array of effector proteins, but progress in characterizing the spatiotemporal localization of these proteins has been hindered by a paucity of genetic approaches in Chlamydia and also by the challenge of studying these proteins within the live cellular environment. We adapted a split-green fluorescent protein (GFP) system for use in Chlamydia to label chlamydial effector proteins and track their localization in host cells under native environment. The efficacy of this system was demonstrated by detecting several known Chlamydia proteins including IncA, CT005 and CT694. We further used this approach to detect two chlamydial deubiquitinases (CT867 and CT868) within live cells during the infection. CT868 localized only to the inclusion membrane at early and late developmental stages. CT867 localized to the chlamydial inclusion membrane at an early developmental stage and was concomitantly localized to the host plasma membrane at a late stage during the infection. These data suggest that chlamydial deubiquitinase play important roles for chlamydial pathogenesis by targeting proteins at both the plasma membrane and the chlamydial inclusion membrane. The split-GFP technology was demonstrated to be a robust and efficient approach to identify the secretion and cellular localization of important chlamydial virulence factors.

Indexed as

Bacterial ProteinsEpithelial CellsGenes, ReporterGreen Fluorescent ProteinsHeLa CellsHumansRecombinant Fusion ProteinsSpatio-Temporal AnalysisStaining and LabelingVirulence FactorsBacterial ProteinsGreen Fluorescent ProteinsRecombinant Fusion ProteinsVirulence Factors

Identifiers

PMID29390129
PMCPMC6251622
OpenAlexW2794086022

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.