Evidence map›Paper›PMID 31103782›Full record

ArticleInsect biochemistry and molecular biology2019

Induction of RNA interference to block Zika virus replication and transmission in the mosquito Aedes aegypti.

Tereza Magalhaes, Nicholas A Bergren, Susan L Bennett, Erin M Borland, Daniel A Hartman, Konstantinos Lymperopoulos, Richard Sayre, Bradley R Borlee, Corey L Campbell, Brian D Foy and 4 more

Open access · greenAbstract read
In one paragraph

Article in Insect biochemistry and molecular biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

13 citing papers in PubMed, 26 citations in OpenAlex.

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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

14 authors at 1 institution in 1 country.

Tereza MagalhaesColorado State, University, Department of Microbiology, Immunology and Pathology, Arthropod-borne and Infectious Diseases Laboratory (AIDL), Fort Collins, CO, 80523, USA. Electronic address: Tereza.Magalhaes@colostate.edu.
Nicholas A BergrenColorado State, University, Department of Microbiology, Immunology and Pathology, Arthropod-borne and Infectious Diseases Laboratory (AIDL), Fort Collins, CO, 80523, USA. Electronic address: Nicholas.Bergren@colostate.edu.
Susan L BennettColorado State, University, Department of Microbiology, Immunology and Pathology, Arthropod-borne and Infectious Diseases Laboratory (AIDL), Fort Collins, CO, 80523, USA. Electronic address: Susi.Bennett@colostate.edu.
Erin M BorlandColorado State, University, Department of Microbiology, Immunology and Pathology, Arthropod-borne and Infectious Diseases Laboratory (AIDL), Fort Collins, CO, 80523, USA. Electronic address: Erin.Borland@colostate.edu.
Daniel A HartmanColorado State, University, Department of Microbiology, Immunology and Pathology, Arthropod-borne and Infectious Diseases Laboratory (AIDL), Fort Collins, CO, 80523, USA. Electronic address: Daniel.Anthony.Hartman@colostate.edu.
Konstantinos LymperopoulosPebble Labs USA Inc., Little Fly Division, Los Alamos, NM, 87544, USA. Electronic address: klymperopoulos@pebblelabs.com.
Richard SayrePebble Labs USA Inc., Little Fly Division, Los Alamos, NM, 87544, USA. Electronic address: rsayre@pebblelabs.com.
Bradley R BorleeColorado State, University, Department of Microbiology, Immunology and Pathology, Arthropod-borne and Infectious Diseases Laboratory (AIDL), Fort Collins, CO, 80523, USA. Electronic address: Brad.Borlee@colostate.edu.
Corey L CampbellColorado State, University, Department of Microbiology, Immunology and Pathology, Arthropod-borne and Infectious Diseases Laboratory (AIDL), Fort Collins, CO, 80523, USA. Electronic address: Corey.Campbell@colostate.edu.
Brian D FoyColorado State, University, Department of Microbiology, Immunology and Pathology, Arthropod-borne and Infectious Diseases Laboratory (AIDL), Fort Collins, CO, 80523, USA. Electronic address: Brian.Foy@colostate.edu.
Kenneth E OlsonColorado State, University, Department of Microbiology, Immunology and Pathology, Arthropod-borne and Infectious Diseases Laboratory (AIDL), Fort Collins, CO, 80523, USA. Electronic address: Kenneth.Olson@colostate.edu.
Carol D BlairColorado State, University, Department of Microbiology, Immunology and Pathology, Arthropod-borne and Infectious Diseases Laboratory (AIDL), Fort Collins, CO, 80523, USA. Electronic address: Carol.Blair@colostate.edu.
William BlackColorado State, University, Department of Microbiology, Immunology and Pathology, Arthropod-borne and Infectious Diseases Laboratory (AIDL), Fort Collins, CO, 80523, USA. Electronic address: William.Black@colostate.edu.
Rebekah C KadingColorado State, University, Department of Microbiology, Immunology and Pathology, Arthropod-borne and Infectious Diseases Laboratory (AIDL), Fort Collins, CO, 80523, USA. Electronic address: Rebekah.Kading@colostate.edu.
Colorado State University · US

Funding

Engineering resistance to Zika virus in Aedes aegypti for Cas9 driven population modificationR01AI130085 · NIAID · COLORADO STATE UNIVERSITY · PI OLSON, KENNETH E · 2018 to 2021
$2.7M
Zika virus urogenital tropism, pathogenesis and sexual transmissionR21AI129464 · NIAID · COLORADO STATE UNIVERSITY · PI FOY, BRIAN DAVID · 2017 to 2018
$377k
NIAID NIH HHS R01 AI130085NIAID NIH HHS R21 AI129464
6 · The paper itself

Abstract

The yellow fever mosquito, Aedes aegypti, serves as the primary vector for epidemic transmission of yellow fever, dengue, Zika (ZIKV), and chikungunya viruses to humans. Control of Ae. aegypti is currently limited to insecticide applications and larval habitat management; however, to combat growing challenges with insecticide resistance, novel genetic approaches for vector population reduction or transmission interruption are being aggressively pursued. The objectives of this study were to assess the ability of the Ae. aegypti antiviral exogenous-small interfering RNA (exo-siRNA) response to inhibit ZIKV infection and transmission, and to identify the optimal RNA interference (RNAi) target region in the ZIKV genome. We accomplished these objectives by in vitro transcription of five long double-stranded RNAs (dsRNAs) from the genome region spanning the NS2B-NS3-NS4A genes, which were the most highly conserved among ZIKV RNA sequences representing both East and West African and Asian-American clades, and evaluation of the ability of these dsRNAs to trigger an effective antiviral exo-siRNA response after intrathoracic injection into Ae. aegypti. In a pilot study, five ZIKV dsRNAs were tested by intrathoracic inoculation of 250 ng dsRNA into groups of approximately 5-day-old mosquitoes. Three days post-inoculation, mosquitoes were provided an infectious blood-meal containing ZIKV strain PRVABC59 (Puerto Rico), MR766 (Uganda), or 41525 (Senegal). On days 7 and 14 post-infection individual whole mosquito bodies were assessed for ZIKV infectious titer by plaque assays. Based on the results of this initial assessment, three dsRNAs were selected for further evaluation of viral loads of matched body and saliva expectorants using a standardized infectious dose of 1 × 10

Indexed as

RNA InterferenceAedesAnimalsCattleChlorocebus aethiopsMosquito VectorsPilot ProjectsRNA, Double-StrandedRNA, Small InterferingSalivaSequence Analysis, RNAVero CellsViral LoadVirus ReplicationZika VirusZika Virus InfectionRNA, Double-StrandedRNA, Small Interfering

Identifiers

PMID31103782
PMCPMC7012353
OpenAlexW2946397801

What OpenQuestion holds

Textmetadata
LicenceTDM
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.