Evidence map›Paper›PMID 26795869›Full record

ReviewVirus research2016

Systems biology: A tool for charting the antiviral landscape.

James R Bowen, Martin T Ferris, Mehul S Suthar

Open access · greenAbstract readReview
In one paragraph

Review in Virus research, 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
0.6field-weighted citation impact, top 32% 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. Article
  2. Article
  3. A dissection of SARS‑CoV2 with clinical implications (Review).International journal of molecular medicine · 2020
    Review
  4. Article
  5. Review
  6. 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

3 authors at 3 institutions in 1 country.

James R BowenDepartment of Pediatrics and Children's Healthcare of Atlanta, Emory University School of Medicine, Atlanta, GA 30329, USA; Emory Vaccine Center, Yerkes National Primate Research Center, Atlanta, GA 30329, USA.
Martin T FerrisDepartment of Genetics, University of North Carolina at Chapel Hill, Chapel Hill NC 27599, USA.
Mehul S SutharDepartment of Pediatrics and Children's Healthcare of Atlanta, Emory University School of Medicine, Atlanta, GA 30329, USA; Emory Vaccine Center, Yerkes National Primate Research Center, Atlanta, GA 30329, USA. Electronic address: mehul.s.suthar@emory.edu.
Emory Healthcare · USEmory University · USUniversity of North Carolina at Chapel Hill · US

Funding

Systems Biology Identifies Restriction Factors for West Nile VirusU19AI106772 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI WATERS, KATRINA M. · 2013 to 2017
$26.1M
West Nile Virus and host control of innate defensesU19AI083019 · NIAID · UNIVERSITY OF WASHINGTON · PI GALE, MICHAEL · 2009 to 2018
$22.5M
Identifying host genetic determinants that regulate dendritic cell activationR21AI113485 · NIAID · EMORY UNIVERSITY · PI SUTHAR, MEHUL SHAMAL · 2015 to 2016
$494k
Regulation of T cell immunity by the cytosolic RIG-I like receptorsR56AI110516 · NIAID · EMORY UNIVERSITY · PI SUTHAR, MEHUL SHAMAL · 2014 to 2014
$443k
Generation of MAVS conditional KO mice to study cell-type specific immunityR03AI109194 · NIAID · EMORY UNIVERSITY · PI SUTHAR, MEHUL SHAMAL · 2014 to 2015
$179k
NIAID NIH HHS R03 AI109194NIAID NIH HHS R21 AI113485NIAID NIH HHS R56 AI110516NIAID NIH HHS U19 AI083019NIAID NIH HHS U19 AI106772
6 · The paper itself

Abstract

The host antiviral programs that are initiated following viral infection form a dynamic and complex web of responses that we have collectively termed as "the antiviral landscape". Conventional approaches to studying antiviral responses have primarily used reductionist systems to assess the function of a single or a limited subset of molecules. Systems biology is a holistic approach that considers the entire system as a whole, rather than individual components or molecules. Systems biology based approaches facilitate an unbiased and comprehensive analysis of the antiviral landscape, while allowing for the discovery of emergent properties that are missed by conventional approaches. The antiviral landscape can be viewed as a hierarchy of complexity, beginning at the whole organism level and progressing downward to isolated tissues, populations of cells, and single cells. In this review, we will discuss how systems biology has been applied to better understand the antiviral landscape at each of these layers. At the organismal level, the Collaborative Cross is an invaluable genetic resource for assessing how genetic diversity influences the antiviral response. Whole tissue and isolated bulk cell transcriptomics serves as a critical tool for the comprehensive analysis of antiviral responses at both the tissue and cellular levels of complexity. Finally, new techniques in single cell analysis are emerging tools that will revolutionize our understanding of how individual cells within a bulk infected cell population contribute to the overall antiviral landscape.

Indexed as

AnimalsDengue VirusEbolavirusHemorrhagic Fever, EbolaHost-Pathogen InteractionsHumansInfluenza A virusInfluenza, HumanRotavirusRotavirus InfectionsSevere DengueSingle-Cell AnalysisSystems BiologyWest Nile FeverWest Nile virusAntiviral responseCollaborative CrossSingle cell analysisSystems biologyTranscriptomicsVirology

Identifiers

PMID26795869
PMCPMC4902762
OpenAlexW2234073726

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.