Evidence map›Paper›PMID 26491875›Full record

ArticlePLoS pathogens2015

Dengue Virus Infection of Aedes aegypti Requires a Putative Cysteine Rich Venom Protein.

Berlin Londono-Renteria, Andrea Troupin, Michael J Conway, Diana Vesely, Michael Ledizet, Christopher M Roundy, Erin Cloherty, Samuel Jameson, Dana Vanlandingham, Stephen Higgs and 2 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
8.9field-weighted citation impact, top 2% 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

27 citing papers in PubMed, 59 citations in OpenAlex.

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  16. Molecular Responses to the Zika Virus in Mosquitoes.Pathogens (Basel, Switzerland) · 2018
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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

12 authors at 5 institutions in 1 country.

Berlin Londono-RenteriaDepartment of Pathology, Microbiology & Immunology, University of South Carolina School of Medicine, Columbia, South Carolina, United States of America.
Andrea TroupinDepartment of Pathology, Microbiology & Immunology, University of South Carolina School of Medicine, Columbia, South Carolina, United States of America.
Michael J ConwayFoundational Sciences, Central Michigan University College of Medicine, Mount Pleasant, Michigan, United States of America.
Diana VeselyL2 Diagnostics, New Haven, Connecticut, United States of America.
Michael LedizetL2 Diagnostics, New Haven, Connecticut, United States of America.
Christopher M RoundyDepartment of Tropical Medicine, Tulane University School of Public Health and Tropical Medicine, New Orleans, Louisiana, United States of America.
Erin ClohertyDepartment of Tropical Medicine, Tulane University School of Public Health and Tropical Medicine, New Orleans, Louisiana, United States of America.
Samuel JamesonDepartment of Tropical Medicine, Tulane University School of Public Health and Tropical Medicine, New Orleans, Louisiana, United States of America.
Dana VanlandinghamBiosecurity Research Institute, Kansas State University, Manhattan, Kansas, United States of America; Diagnostic Medicine and Pathobiology, Kansas State University, Manhattan, Kansas, United States of America.
Stephen HiggsBiosecurity Research Institute, Kansas State University, Manhattan, Kansas, United States of America; Diagnostic Medicine and Pathobiology, Kansas State University, Manhattan, Kansas, United States of America.
Erol FikrigSection of Infectious Diseases, Department of Internal Medicine, Yale University School of Medicine, New Haven, Connecticut, United States of America; Howard Hughes Medical Institute, Chevy Chase, Maryland, United States of America.
Tonya M ColpittsDepartment of Pathology, Microbiology & Immunology, University of South Carolina School of Medicine, Columbia, South Carolina, United States of America.
Tulane University · USUniversity of South Carolina · USKansas State University · USCentral Michigan University · USHoward Hughes Medical Institute · US

Funding

Targeting early ceramide elevation in pre-symptomatic eczemaP20GM103641 · NIGMS · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI ENOS, REILLY, NAGARKATTI, PRAKASH S · 2012 to 2023
$20.7M
IMMUNOHEMATOLOGY/TRANSFUSION MEDICINE RESEARCH TRAININGT32HL007974 · NHLBI · YALE UNIVERSITY · PI JEANNE E HENDRICKSON, Diane S Krause · 2001 to 2026
$8.1M
Immunotherapeutics for Treatment of Flavivirus InfectionU01AI070343 · NIAID · YALE UNIVERSITY · PI FIKRIG, EROL · 2006 to 2010
$6.6M
The antiviral role of mosquito ubiquitin Ub3881 during dengue infectionK22AI103067 · NIAID · TULANE UNIVERSITY OF LOUISIANA · PI COLPITTS, TONYA MICHELLE · 2013 to 2014
$270k
Howard Hughes Medical InstituteNHLBI NIH HHS T32 HL007974NIAID NIH HHS K22 AI103067NIAID NIH HHS K22AI103067NIAID NIH HHS U01 AI070343NIAID NIH HHS U01AI070343NIGMS NIH HHS P20 GM103641
6 · The paper itself

Abstract

Dengue virus (DENV) is a mosquito-borne flavivirus that causes serious human disease and mortality worldwide. There is no specific antiviral therapy or vaccine for DENV infection. Alterations in gene expression during DENV infection of the mosquito and the impact of these changes on virus infection are important events to investigate in hopes of creating new treatments and vaccines. We previously identified 203 genes that were ≥5-fold differentially upregulated during flavivirus infection of the mosquito. Here, we examined the impact of silencing 100 of the most highly upregulated gene targets on DENV infection in its mosquito vector. We identified 20 genes that reduced DENV infection by at least 60% when silenced. We focused on one gene, a putative cysteine rich venom protein (SeqID AAEL000379; CRVP379), whose silencing significantly reduced DENV infection in Aedes aegypti cells. Here, we examine the requirement for CRVP379 during DENV infection of the mosquito and investigate the mechanisms surrounding this phenomenon. We also show that blocking CRVP379 protein with either RNAi or specific antisera inhibits DENV infection in Aedes aegypti. This work identifies a novel mosquito gene target for controlling DENV infection in mosquitoes that may also be used to develop broad preventative and therapeutic measures for multiple flaviviruses.

Indexed as

AedesAnimalsArthropod VenomsBlotting, WesternCysteineDengueDengue VirusEnzyme-Linked Immunosorbent AssayFluorescent Antibody TechniqueGene SilencingInsect ProteinsInsect VectorsPolymerase Chain ReactionRNA, Small InterferingTransfectionArthropod VenomsCysteineInsect ProteinsRNA, Small Interfering

Identifiers

PMID26491875
PMCPMC4619585
OpenAlexW2161860613

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.