Evidence map›Paper›PMID 26752057›Full record

ArticlePloS one2016

Tools for Single-Cell Kinetic Analysis of Virus-Host Interactions.

Jay W Warrick, Andrea Timm, Adam Swick, John Yin

Abstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
–field-weighted citation impact
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

32 citing papers in PubMed.

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  18. Mammary adipose stromal cells derived from obese women reduce sensitivity to the aromatase inhibitor anastrazole in an organotypic breast model.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
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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.

Jay W WarrickSystems Biology Theme, Wisconsin Institute for Discovery, Department of Chemical and Biological Engineering, University of Wisconsin-Madison, Madison, WI, United States of America.
Andrea TimmSystems Biology Theme, Wisconsin Institute for Discovery, Department of Chemical and Biological Engineering, University of Wisconsin-Madison, Madison, WI, United States of America.
Adam SwickSystems Biology Theme, Wisconsin Institute for Discovery, Department of Chemical and Biological Engineering, University of Wisconsin-Madison, Madison, WI, United States of America.
John YinSystems Biology Theme, Wisconsin Institute for Discovery, Department of Chemical and Biological Engineering, University of Wisconsin-Madison, Madison, WI, United States of America.

Funding

Wisconsin Infant Study Cohort (WISC)U19AI104317 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI Irene M Ong · 2013 to 2026
$22.5M
RV-Mediated Mechanisms of Neutrophil Motility /InflammatU19AI070503 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI GERN, JAMES E. · 2006 to 2010
$6.8M
Virology Training ProgramT32AI078985 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI LAMBERT, PAUL F. · 2009 to 2018
$3.3M
Evolution of Virus-Host InteractionsR01AI091646 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI YIN, JOHN · 2011 to 2015
$2.0M
NIAID NIH HHS R01 AI091646NIAID NIH HHS R01-AI091646NIAID NIH HHS T32 AI078985NIAID NIH HHS T32-AI078985NIAID NIH HHS U19-AI0104317NIAID NIH HHS U19 AI070503NIAID NIH HHS U19 AI104317
6 · The paper itself

Abstract

Measures of cellular gene expression or behavior, when performed on individual cells, inevitably reveal a diversity of behaviors and outcomes that can correlate with normal or diseased states. For virus infections, the potential diversity of outcomes are pushed to an extreme, where measures of infection reflect features of the specific infecting virus particle, the individual host cell, as well as interactions between viral and cellular components. Single-cell measures, while revealing, still often rely on specialized fluid handling capabilities, employ end-point measures, and remain labor-intensive to perform. To address these limitations, we consider a new microwell-based device that uses simple pipette-based fluid handling to isolate individual cells. Our design allows different experimental conditions to be implemented in a single device, permitting easier and more standardized protocols. Further, we utilize a recently reported dual-color fluorescent reporter system that provides dynamic readouts of viral and cellular gene expression during single-cell infections by vesicular stomatitis virus. In addition, we develop and show how free, open-source software can enable streamlined data management and batch image analysis. Here we validate the integration of the device and software using the reporter system to demonstrate unique single-cell dynamic measures of cellular responses to viral infection.

Indexed as

Gene Expression RegulationSoftwareApoptosis Regulatory ProteinsCell Line, TumorDEAD Box Protein 58DEAD-box RNA HelicasesEpithelial CellsFluorescent DyesGenes, ReporterGreen Fluorescent ProteinsHigh-Throughput Screening AssaysHost-Pathogen InteractionsHumansInterferon Regulatory Factor-3Interferon Regulatory Factor-7Interferon Type IApoptosis Regulatory ProteinsDEAD Box Protein 58DEAD-box RNA HelicasesFluorescent DyesGreen Fluorescent ProteinsIFIT2 protein, humanInterferon Regulatory Factor-3Interferon Regulatory Factor-7Interferon Type IIRF3 protein, humanIRF7 protein, humanLuminescent ProteinsProteinsReceptors, ImmunologicRed Fluorescent ProteinRIGI protein, humanRNA-Binding Proteins

Identifiers

PMID26752057
PMCPMC4713429

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.