Evidence map›Paper›PMID 31136639›Full record

ArticlePloS one2019

Transcriptome profiling in Rift Valley fever virus infected cells reveals modified transcriptional and alternative splicing programs.

Katherine E Havranek, Luke Adam White, Jean-Marc Lanchy, J Stephen Lodmell

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

18 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
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  6. Mechanism of Immune Evasion in Mosquito-Borne Diseases.Pathogens (Basel, Switzerland) · 2023
    Review
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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 at 1 institution in 1 country.

Katherine E HavranekDivision of Biological Sciences, The University of Montana, Missoula, MT, United States of America.
Luke Adam WhiteDivision of Biological Sciences, The University of Montana, Missoula, MT, United States of America.ORCID 0000-0003-4548-0661
Jean-Marc LanchyDivision of Biological Sciences, The University of Montana, Missoula, MT, United States of America.
J Stephen LodmellDivision of Biological Sciences, The University of Montana, Missoula, MT, United States of America.ORCID 0000-0002-8087-5362
University of Montana · US

Funding

Surveillance genome sequencing to detect SARS-CoV-2 virus variants in MontanaP20GM103546 · NIGMS · UNIVERSITY OF MONTANA · PI BOWLER, BRUCE E · 2012 to 2021
$19.2M
Mechanism of RVFV nucleocapsid targeting drugsR15AI105737 · NIAID · UNIVERSITY OF MONTANA · PI LODMELL, J. STEPHEN · 2014 to 2014
$432k
A role for snoRNAs in RVFV-induced enhancement of alternative splicingR03AI137620 · NIAID · UNIVERSITY OF MONTANA · PI LODMELL, J. STEPHEN · 2019 to 2020
$145k
Integrated Phosphor and Fluorescence Imager (Typhoon FLA9500)S10OD021710 · OD · UNIVERSITY OF MONTANA · PI NUNBERG, JACK H · 2016 to 2016
$138k
NIAID NIH HHS R03 AI137620NIAID NIH HHS R15 AI105737NIGMS NIH HHS P20 GM103546NIH HHS S10 OD021710
6 · The paper itself

Abstract

Rift Valley fever virus (RVFV) is a negative-sense RNA virus belonging to the Phenuiviridae family that infects both domestic livestock and humans. The NIAID has designated RVFV as a Category A priority emerging pathogen due to the devastating public health outcomes associated with epidemic outbreaks. However, there is no licensed treatment or vaccine approved for human use. Therefore it is of great interest to understand RVFV pathogenesis in infected hosts in order to facilitate creation of targeted therapies and treatment options. Here we provide insight into the host-pathogen interface in human HEK293 cells during RVFV MP-12 strain infection using high-throughput mRNA sequencing technology. Gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis of differentially expressed genes showed robust innate immune and cytokine-mediated inflammatory pathway activation as well as alterations in pathways associated with fatty acid metabolism and extracellular matrix receptor signaling. We also analyzed the promoter regions of DEGs for patterns in transcription factor binding sites, and found several that are known to act synergistically to impact apoptosis, immunity, metabolism, and cell growth and differentiation. Lastly, we noted dramatic changes in host alternative splicing patterns in genes associated with mRNA decay and surveillance, RNA transport, and DNA repair. This study has improved our understanding of RVFV pathogenesis and has provided novel insight into pathways and signaling modules important for RVFV diagnostics and therapeutic development.

Indexed as

Alternative SplicingGene Expression ProfilingGene Expression Regulation, ViralTranscription, GeneticHEK293 CellsHumansRift Valley FeverRift Valley fever virus

Identifiers

PMID31136639
PMCPMC6538246
OpenAlexW2947099818

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.