Evidence map›Paper›PMID 26567000›Full record

ArticleThe Journal of eukaryotic microbiology2016

A Novel Fluorescent Labeling Method Enables Monitoring of Spatio-Temporal Dynamics of Developing Microsporidia.

Marianita Santiana, Peter M Takvorian, Nihal Altan-Bonnet, Ann Cali

Abstract read
In one paragraph

Article in The Journal of eukaryotic microbiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. Heterologous Expressed NbSWP12 from MicrosporidiaJournal of fungi (Basel, Switzerland) · 2022
    Article
  4. Human microsporidian pathogenJournal of cell science · 2021
    Article
  5. Article
  6. 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

4 authors at 3 institutions in 1 country.

Marianita SantianaFederated Department of Biological Sciences, Rutgers University, Newark, New Jersey, 07102.
Peter M TakvorianFederated Department of Biological Sciences, Rutgers University, Newark, New Jersey, 07102.
Nihal Altan-BonnetLaboratory of Host-Pathogen Dynamics, Cell Biology and Physiology Center, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, Maryland 20892.
Ann CaliFederated Department of Biological Sciences, Rutgers University, Newark, New Jersey, 07102.
Rutgers, The State University of New Jersey · USNational Heart Lung and Blood Institute · USNational Institutes of Health · US

Funding

Virus Egress PathwaysZIAHL006234 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI ALTAN-BONNET, NIHAL · 2017 to 2025
$21.8M
New Opportunistic Infections in AIDS MicrosporidosisR01AI031788 · NIAID · YESHIVA UNIVERSITY · PI WEISS, LOUIS M. · 1992 to 2011
$4.6M
Assembly dynamics and role of PI4P enriched replication organelles for enteroviraR01AI091985 · NIAID · RUTGERS THE STATE UNIV OF NJ NEWARK · PI CALI, ANN · 2011 to 2015
$2.0M
Intramural NIH HHS Z99 HL999999NIAID NIH HHS R01 AI031788NIAID NIH HHS R01 AI091985
6 · The paper itself

Abstract

The microsporidium, Anncaliia algerae (Brachiola algerae), is a eukaryotic obligate intracellular parasite first isolated from mosquitoes and is an important opportunistic human pathogen that can cause morbidity and mortality among immune-compromised individuals including patients with AIDS and those undergoing chemotherapy. There is little known about the Microsporidia-host cell interface in living host cells, due to current approaches being limited by the lack of fluorescent reporters for detecting the parasite lifecycle. Here, we have developed and applied novel vital fluorescent parasite labeling methodologies in conjunction with fluorescent protein-tagged reporters to track simultaneously the dynamics of both parasite and host cell specific components, including the secretory and endocytic trafficking pathways, during the entire infection time period. We have found dramatic changes in the dynamics of host secretory trafficking organelles during the course of infection. The Golgi compartment is gradually disassembled and regenerated into mini-Golgi structures in parallel with cellular microtubule depolymerization. Importantly, we find that Microsporidia progeny are associated with these de novo formed mini-Golgi structures. These host structures appear to create a membrane bound niche environment for parasite development. Our studies presented here provide novel imaging tools and methodologies that will facilitate in understanding the biology of microsporidial parasites in the living host.

Indexed as

Spatio-Temporal AnalysisGolgi ApparatusHeLa CellsHost-Parasite InteractionsHumansLife Cycle StagesMicroscopy, ConfocalMicroscopy, FluorescenceMicrosporidia, UnclassifiedMicrotubulesSpores, FungalStaining and LabelingTransport VesiclesAnncaliia algeraeArf-1-GFPDRAQ5Golgi, HeLa cellslive imagingmicrotubulesorganelle hijacking

Identifiers

PMID26567000
PMCPMC6726495
OpenAlexW2180186440

What OpenQuestion holds

Textmetadata
LicenceTDM
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.