Evidence map›Paper›PMID 30638014›Full record

ArticleBiochemistry2019

A Microfluidic-Based Microscopy Platform for Continuous Interrogation of Trypanosoma brucei during Environmental Perturbation.

Charles M Voyton, Jongsu Choi, Yijian Qiu, Meredith T Morris, P Christine Ackroyd, James C Morris, Kenneth A Christensen

Abstract read
In one paragraph

Article in Biochemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 34% 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

3 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

7 authors at 2 institutions in 1 country.

Charles M VoytonDepartment of Chemistry , Clemson University , Clemson , South Carolina 29634 , United States.
Jongsu ChoiDepartment of Chemistry and Biochemistry , Brigham Young University , Provo , Utah 84602 , United States.
Yijian QiuEukaryotic Pathogens Innovation Center, Department of Genetics and Biochemistry , Clemson University , Clemson , South Carolina 29634 , United States.
Meredith T MorrisEukaryotic Pathogens Innovation Center, Department of Genetics and Biochemistry , Clemson University , Clemson , South Carolina 29634 , United States.
P Christine AckroydDepartment of Chemistry and Biochemistry , Brigham Young University , Provo , Utah 84602 , United States.
James C MorrisEukaryotic Pathogens Innovation Center, Department of Genetics and Biochemistry , Clemson University , Clemson , South Carolina 29634 , United States.
Kenneth A ChristensenDepartment of Chemistry , Clemson University , Clemson , South Carolina 29634 , United States.ORCID 0000-0002-3736-5500
Brigham Young University · USClemson University · US

Funding

The role of acetate fermentation in Entamoeba histolytica growth and infectionP20GM109094 · NIGMS · CLEMSON UNIVERSITY · PI TEMESVARI, LESLY A · 2016 to 2020
$10.4M
Identification of kinetoplastid parasite glucose uptake and subcellular localization inhibitors as therapeutic leadsR21AI127575 · NIAID · CLEMSON UNIVERSITY · PI CHRISTENSEN, KENNETH A, GOLDEN, JENNIFER E. · 2017 to 2018
$456k
pH and glucose sensing in Trypanosoma brucei glycosomesR21AI105656 · NIAID · CLEMSON UNIVERSITY · PI CHRISTENSEN, KENNETH A, MORRIS, JAMES CULVIN · 2014 to 2015
$382k
NIAID NIH HHS R21 AI105656NIAID NIH HHS R21 AI127575NIGMS NIH HHS P20 GM109094
6 · The paper itself

Abstract

The African trypanosome, Trypanosoma brucei, is the causative agent of human African trypanosomiasis (HAT). African trypanosomes are extracellular parasites that possess a single flagellum that imparts a high degree of motility to the microorganisms. In addition, African trypanosomes show significant metabolic and structural adaptation to environmental conditions. Analysis of the ways that environmental cues affect these organisms generally requires rapid perfusion experiments in combination with single-cell imaging, which are difficult to apply under conditions of rapid motion. Microfluidic devices have been used previously as a strategy for trapping small motile cells in a variety of organisms, including trypanosomes; however, in the past, such devices required individual fabrication in a cleanroom, limiting their application. Here we demonstrate that a commercial microfluidic device, typically used for bacterial trapping, can trap bloodstream and procyclic form trypanosomes, allowing for rapid buffer exchange via perfusion. As a result, time-lapse single-cell microscopy images of these highly motile parasites were acquired during environmental variations. Using these devices, we have been able to perform and analyze perfusion-based single-cell tracking experiments of the responses of the parasite to changes in glucose availability, which is a major step in resolving the mechanisms of adaptation of kinetoplasts to their individual biological niches; we demonstrate utility of this tool for making measurements of procyclic form trypanosome intracellular glucose levels as a function of changes in extracellular glucose concentrations. These experiments demonstrate that cytosolic glucose equilibrates with external conditions as fast as, or faster than, the rate of solution exchange in the instrument.

Indexed as

Lab-On-A-Chip DevicesFluoresceinGlucoseMicroscopy, FluorescenceSingle-Cell AnalysisTime-Lapse ImagingTrypanosoma brucei bruceiFluoresceinGlucose

Identifiers

PMID30638014
PMCPMC6463508
OpenAlexW2910919149

What OpenQuestion holds

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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.