Evidence map›Paper›PMID 27066744›Full record

ArticleCell host & microbe2016

A Mouse Model of Zika Virus Pathogenesis.

Helen M Lazear, Jennifer Govero, Amber M Smith, Derek J Platt, Estefania Fernandez, Jonathan J Miner, Michael S Diamond

Open access · bronzeAbstract read
In one paragraph

Article in Cell host & microbe, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 662 papers.

0numbers the graph read from it
0cells of the map it votes in
662citing papers in PubMed
158.9field-weighted citation impact, top 1% 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

662 citing papers in PubMed, 911 citations in OpenAlex.

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602 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Helen M LazearDepartment of Microbiology and Immunology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Jennifer GoveroDepartment of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.
Amber M SmithDepartment of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.
Derek J PlattDepartment of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.
Estefania FernandezDepartment of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.
Jonathan J MinerDepartment of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.
Michael S DiamondDepartment of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA; Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO 63110, USA; Department of Pathology & Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA; The Center for Human Immunology and Immunotherapy Programs, Washington University School of Medicine, St. Louis, MO 63110, USA. Electronic address: diamond@borcim.wustl.edu.
Washington University in St. Louis · USUniversity of North Carolina at Chapel Hill · US

Funding

TRAINING PROGRAM IN IMMUNOLOGY AND IMMUNOGENETICST32AI007163 · NIAID · WASHINGTON UNIVERSITY · PI Kenneth M Murphy, Kodi S Ravichandran · 1985 to 2026
$14.8M
Antibody-based Protection against FlavivirsesR01AI073755 · NIAID · WASHINGTON UNIVERSITY · PI DIAMOND, MICHAEL S, FREMONT, DAVED H. · 2007 to 2022
$11.4M
OPPORTUNITIES IN GENOMICS RESEARCH: INCREASING DIVERSITY AND RETENTION IN STEMR25HG006687 · NHGRI · WASHINGTON UNIVERSITY · PI MITRA, ROBI D, SKEATH, JAMES BENJAMIN · 2012 to 2025
$4.1M
ISG CONTROL OF FLAVIVIRUS INFECTIONR01AI104972 · NIAID · WASHINGTON UNIVERSITY · PI CHANDA, SUMIT K, DIAMOND, MICHAEL S · 2013 to 2017
$3.0M
NHGRI NIH HHS R25 HG006687NIAID NIH HHS R01 AI073755NIAID NIH HHS R01 AI104972NIAID NIH HHS T32 AI007163
6 · The paper itself

Abstract

The ongoing Zika virus (ZIKV) epidemic and unexpected clinical outcomes, including Guillain-Barré syndrome and birth defects, has brought an urgent need for animal models. We evaluated infection and pathogenesis with contemporary and historical ZIKV strains in immunocompetent mice and mice lacking components of the antiviral response. Four- to six-week-old Irf3(-/-)Irf5(-/-)Irf7(-/-) triple knockout mice, which produce little interferon α/β, and mice lacking the interferon receptor (Ifnar1(-/-)) developed neurological disease and succumbed to ZIKV infection, whereas single Irf3(-/-), Irf5(-/-), and Mavs(-/-) knockout mice exhibited no overt illness. Ifnar1(-/-) mice sustained high viral loads in the brain and spinal cord, consistent with evidence that ZIKV causes neurodevelopmental defects in human fetuses. The testes of Ifnar1(-/-) mice had the highest viral loads, which is relevant to sexual transmission of ZIKV. This model of ZIKV pathogenesis will be valuable for evaluating vaccines and therapeutics as well as understanding disease pathogenesis.

Indexed as

Disease Models, AnimalAnimalsChlorocebus aethiopsHumansMaleMiceMice, Inbred C57BLMice, KnockoutVero CellsZika VirusZika Virus Infection

Identifiers

PMID27066744
PMCPMC4866885
OpenAlexW2327959547

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.