Evidence map›Paper›PMID 26442221›Full record

ArticleFrontiers in cellular and infection microbiology2015

The trans-Golgi SNARE syntaxin 10 is required for optimal development of Chlamydia trachomatis.

Andrea L Lucas, Scot P Ouellette, Emily J Kabeiseman, Kyle H Cichos, Elizabeth A Rucks

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

16 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Review
  3. mSphere · 2024
    Article
  4. Article
  5. Establishing the intracellular niche of obligate intracellular vacuolar pathogens.Frontiers in cellular and infection microbiology · 2023
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Chlamydial Infection From Outside to Inside.Frontiers in microbiology · 2019
    Review
  13. Development of a Proximity Labeling System to Map theFrontiers in cellular and infection microbiology · 2017
    Article
  14. Article
  15. Article
  16. Chlamydia cell biology and pathogenesis.Nature reviews. Microbiology · 2016
    Review
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 2 institutions in 1 country.

Andrea L LucasDivision of Basic Biomedical Sciences, Sanford School of Medicine, University of South Dakota Vermillion, SD, USA.
Scot P OuelletteDivision of Basic Biomedical Sciences, Sanford School of Medicine, University of South Dakota Vermillion, SD, USA.
Emily J KabeisemanDivision of Basic Biomedical Sciences, Sanford School of Medicine, University of South Dakota Vermillion, SD, USA.
Kyle H CichosDivision of Basic Biomedical Sciences, Sanford School of Medicine, University of South Dakota Vermillion, SD, USA.
Elizabeth A RucksDivision of Basic Biomedical Sciences, Sanford School of Medicine, University of South Dakota Vermillion, SD, USA.
University of South Dakota · USUniversity of Alabama at Birmingham · US

Funding

Chlamydial lipid acquisition and host responseR15AI107727 · NIAID · UNIVERSITY OF SOUTH DAKOTA · PI RUCKS, ELIZABETH ANN · 2014 to 2014
$443k
Examination of eukaryotic SNARE syntaxin 6 localization to the chlamydial inclusiK22AI089856 · NIAID · UNIVERSITY OF SOUTH DAKOTA · PI RUCKS, ELIZABETH ANN · 2011 to 2012
$264k
NIAID NIH HHS 1K22AI089856-01A1NIAID NIH HHS 1R15AI107727-01A1NIAID NIH HHS K22 AI089856NIAID NIH HHS R15 AI107727
6 · The paper itself

Abstract

Chlamydia trachomatis, an obligate intracellular pathogen, grows inside of a vacuole, termed the inclusion. Within the inclusion, the organisms differentiate from the infectious elementary body (EB) into the reticulate body (RB). The RB communicates with the host cell through the inclusion membrane to obtain the nutrients necessary to divide, thus expanding the chlamydial population. At late time points within the developmental cycle, the RBs respond to unknown molecular signals to redifferentiate into infectious EBs to perpetuate the infection cycle. One strategy for Chlamydia to obtain necessary nutrients and metabolites from the host is to intercept host vesicular trafficking pathways. In this study we demonstrate that a trans-Golgi soluble N-ethylmaleimide-sensitive factor attachment protein (SNARE), syntaxin 10, and/or syntaxin 10-associated Golgi elements colocalize with the chlamydial inclusion. We hypothesized that Chlamydia utilizes the molecular machinery of syntaxin 10 at the inclusion membrane to intercept specific vesicular trafficking pathways in order to create and maintain an optimal intra-inclusion environment. To test this hypothesis, we used siRNA knockdown of syntaxin 10 to examine the impact of the loss of syntaxin 10 on chlamydial growth and development. Our results demonstrate that loss of syntaxin 10 leads to defects in normal chlamydial maturation including: variable inclusion size with fewer chlamydial organisms per inclusion, fewer infectious progeny, and delayed or halted RB-EB differentiation. These defects in chlamydial development correlate with an overabundance of NBD-lipid retained by inclusions cultured in syntaxin 10 knockdown cells. Overall, loss of syntaxin 10 at the inclusion membrane negatively affects Chlamydia. Understanding host machinery involved in maintaining an optimal inclusion environment to support chlamydial growth and development is critical toward understanding the molecular signals involved in successful progression through the chlamydial developmental cycle.

Indexed as

Host-Pathogen InteractionsChlamydia trachomatisEpithelial CellsGene Knockdown TechniquesHeLa CellsHumansInclusion BodiesQa-SNARE ProteinsRNA, Small InterferingQa-SNARE ProteinsRNA, Small Interferingchlamydial developmentChlamydia trachomatislipid traffickingsyntaxin 10trans-Golgi SNARE

Identifiers

PMID26442221
PMCPMC4585193
OpenAlexW2106443737

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.