Evidence map›Paper›PMID 27620201›Full record

ArticlePathogens and disease2016

Conservation of extrusion as an exit mechanism for Chlamydia.

Meghan Zuck, Ashley Sherrid, Robert Suchland, Tisha Ellis, Kevin Hybiske

Open access · bronzeAbstract readLetter
In one paragraph

Article in Pathogens and disease, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

25 citing papers in PubMed, 38 citations in OpenAlex.

  1. Inclusion Membrane Proteins ofMicroorganisms · 2026
    Review
  2. Review
  3. Anti-International journal of molecular sciences · 2026
    Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Journal of bacteriology · 2025
    Review
  9. mBio · 2024
    Article
  10. Article
  11. Insights into innate immune cell evasion byFrontiers in immunology · 2024
    Review
  12. Article
  13. TheInfection and immunity · 2022
    Article
  14. Article
  15. Frontiers in cellular and infection microbiology · 2022
    Review
  16. Article
  17. Article
  18. Murine Endometrial Organoids to ModelFrontiers in cellular and infection microbiology · 2020
    Article
  19. Frontiers in cellular and infection microbiology · 2020
    Article
  20. 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 1 institution in 1 country.

Meghan ZuckDivision of Allergy and Infectious Diseases, Department of Medicine, University of Washington, Seattle, WA, USA Program in Infectious Diseases, School of Public Health, University of California, Berkeley, Berkeley, CA, USA.
Ashley SherridDivision of Allergy and Infectious Diseases, Department of Medicine, University of Washington, Seattle, WA, USA.
Robert SuchlandDivision of Allergy and Infectious Diseases, Department of Medicine, University of Washington, Seattle, WA, USA.
Tisha EllisDivision of Allergy and Infectious Diseases, Department of Medicine, University of Washington, Seattle, WA, USA.
Kevin HybiskeDivision of Allergy and Infectious Diseases, Department of Medicine, University of Washington, Seattle, WA, USA khybiske@uw.edu.
University of Washington · US

Funding

VENEREAL DISEASET32AI007140 · NIAID · UNIVERSITY OF WASHINGTON · PI Julia Cook Dombrowski · 1985 to 2026
$19.4M
Molecular Determinants of Chlamydia Extrusion from Host CellsR01AI095603 · NIAID · UNIVERSITY OF WASHINGTON · PI HYBISKE, KEVIN · 2011 to 2015
$2.0M
NIAID NIH HHS R01 AI095603NIAID NIH HHS T32 AI007140
6 · The paper itself

Abstract

Chlamydiae exit via membrane-encased extrusion or through lysis of the host cell. Extrusions are novel, pathogen-containing structures that confer infectious advantages to Chlamydia, and are hypothesized to promote cell-to-cell spread, dissemination to distant tissues and facilitate immune evasion. The extrusion phenomenon has been characterized for several Chlamydia trachomatis serovars, but a thorough investigation of extrusion for additional clinically relevant C. trachomatis strains and Chlamydia species has yet to be performed. The key parameters investigated in this study were: (i) the conservation of extrusion across the Chlamydia genus, (ii) the functional requirement for candidate Chlamydia genes in extrusion formation i.e. IncA and CT228 and (iii) extrusion-mediated uptake, and consequent survival of Chlamydia inside macrophages. Inclusion morphology was characterized by live fluorescence microscopy, using an inverted GFP strategy, at early and mid-stages of infection. Enriched extrusions were used to infect bone marrow-derived macrophages, and bacterial viability was measured following macrophage engulfment. Our results demonstrate that extrusion is highly conserved across chlamydiae, including ocular, STD and LGV biovars and divergent Chlamydia species. Consequently, this exit mechanism for Chlamydia may fulfill common advantages important for pathogenesis.

Indexed as

Biological EvolutionCell LineCell Surface ExtensionsChlamydiaChlamydia InfectionsHeLa CellsHost-Pathogen InteractionsHumansMacrophagesChlamydiadisseminationexitextrusionmacrophage

Identifiers

PMID27620201
PMCPMC5985487
OpenAlexW2518772581

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.