Evidence map›Paper›PMID 38890352›Full record

ArticleNature communications2024

Disruption of myelin structure and oligodendrocyte maturation in a macaque model of congenital Zika infection.

Jennifer Tisoncik-Go, Caleb Stokes, Leanne S Whitmore, Daniel J Newhouse, Kathleen Voss, Andrew Gustin, Cheng-Jung Sung, Elise Smith, Jennifer Stencel-Baerenwald, Edward Parker and 6 more

Abstract read
In one paragraph

Article in Nature communications, 2024. 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
–field-weighted citation impact
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.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors.

Jennifer Tisoncik-Go *Center for Innate Immunity and Immune Disease, Department of Immunology, University of Washington, Seattle, WA, USA. tisoncik@uw.edu.ORCID http://orcid.org/0000-0003-1381-265X
Caleb Stokes *Center for Innate Immunity and Immune Disease, Department of Immunology, University of Washington, Seattle, WA, USA. caleb.stokes@seattlechildrens.org.ORCID http://orcid.org/0000-0003-3741-0057
Leanne S WhitmoreCenter for Innate Immunity and Immune Disease, Department of Immunology, University of Washington, Seattle, WA, USA.ORCID http://orcid.org/0000-0002-8721-8701
Daniel J NewhouseCenter for Innate Immunity and Immune Disease, Department of Immunology, University of Washington, Seattle, WA, USA.
Kathleen VossCenter for Innate Immunity and Immune Disease, Department of Immunology, University of Washington, Seattle, WA, USA.ORCID http://orcid.org/0000-0003-1033-7670
Andrew GustinCenter for Innate Immunity and Immune Disease, Department of Immunology, University of Washington, Seattle, WA, USA.ORCID http://orcid.org/0000-0002-8760-8320
Cheng-Jung SungCenter for Innate Immunity and Immune Disease, Department of Immunology, University of Washington, Seattle, WA, USA.ORCID http://orcid.org/0000-0001-7858-8308
Elise SmithCenter for Innate Immunity and Immune Disease, Department of Immunology, University of Washington, Seattle, WA, USA.
Jennifer Stencel-BaerenwaldCenter for Innate Immunity and Immune Disease, Department of Immunology, University of Washington, Seattle, WA, USA.
Edward ParkerDepartment of Ophthalmology, NEI Core for Vision Research, University of Washington, Seattle, WA, USA.
Jessica M SnyderDepartment of Comparative Medicine, University of Washington, Seattle, WA, USA.
Dennis W ShawDepartment of Radiology, University of Washington, Seattle, WA, USA.
Lakshmi RajagopalDepartment of Pediatrics, University of Washington, Seattle, WA, USA.ORCID http://orcid.org/0000-0003-3373-2323
Raj P KapurDepartment of Pathology, University of Washington, Seattle, WA, USA.ORCID http://orcid.org/0000-0002-5718-407X
Kristina M Adams WaldorfDepartment of Global Health, University of Washington, Seattle, WA, USA.ORCID http://orcid.org/0000-0002-6939-7224
Michael GaleCenter for Innate Immunity and Immune Disease, Department of Immunology, University of Washington, Seattle, WA, USA. mgale@uw.edu.ORCID http://orcid.org/0000-0002-6332-7436

Funding

Washington National Primate Research CenterP51OD010425 · OD · UNIVERSITY OF WASHINGTON · PI Mari Ostendorf · 2012 to 2026
$201.8M
WaNPRC Macaca nemestrina SPF Breeding ColonyU42OD011123 · OD · UNIVERSITY OF WASHINGTON · PI Melissa R Berg, Cindy Buckmaster · 2012 to 2026
$34.4M
Vision Research CoreP30EY001730 · NEI · UNIVERSITY OF WASHINGTON · PI JAMES Bryant HURLEY · 1985 to 2026
$23.5M
Diseases of Public Health Importance Training GrantT32AI007509 · NIAID · UNIVERSITY OF WASHINGTON · PI LUND, JENNIFER M · 1997 to 2024
$6.3M
JAK-STAT Control of Zika Virus-Induced Fetal InjuryR01AI143265 · NIAID · UNIVERSITY OF WASHINGTON · PI ADAMS WALDORF, KRISTINA M., GALE, MICHAEL · 2019 to 2023
$4.6M
Innate Immune Regulation of Zika Virus InfectionR01AI145296 · NIAID · UNIVERSITY OF WASHINGTON · PI COYNE, CAROLYN B, DIAMOND, MICHAEL S · 2019 to 2023
$4.1M
Innate Immunity of Zika Virus Infection In Human Neural ProgenitorsK08AI150996 · NIAID · UNIVERSITY OF WASHINGTON · PI STOKES, CALEB · 2020 to 2024
$975k
Division of Intramural Research, National Institute of Allergy and Infectious Diseases (Division of Intramural Research of the NIAID) 5R01AI143265NEI NIH HHS P30 EY001730NIAID NIH HHS K08 AI150996NIAID NIH HHS R01 AI143265NIAID NIH HHS R01 AI145296NIAID NIH HHS T32 AI007509NIH HHS P51 OD010425NIH HHS U42 OD011123U.S. Department of Health & Human Services | NIH | National Eye Institute (NEI) P30EY001730U.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases (NIAID) AI145296U.S. Department of Health & Human Services | NIH | NIH Office of the Director (OD) OD010425
6 · The paper itself

Abstract

Zika virus (ZikV) infection during pregnancy can cause congenital Zika syndrome (CZS) and neurodevelopmental delay in infants, of which the pathogenesis remains poorly understood. We utilize an established female pigtail macaque maternal-to-fetal ZikV infection/exposure model to study fetal brain pathophysiology of CZS manifesting from ZikV exposure in utero. We find prenatal ZikV exposure leads to profound disruption of fetal myelin, with extensive downregulation in gene expression for key components of oligodendrocyte maturation and myelin production. Immunohistochemical analyses reveal marked decreases in myelin basic protein intensity and myelinated fiber density in ZikV-exposed animals. At the ultrastructural level, the myelin sheath in ZikV-exposed animals shows multi-focal decompaction, occurring concomitant with dysregulation of oligodendrocyte gene expression and maturation. These findings define fetal neuropathological profiles of ZikV-linked brain injury underlying CZS resulting from ZikV exposure in utero. Because myelin is critical for cortical development, ZikV-related perturbations in oligodendrocyte function may have long-term consequences on childhood neurodevelopment, even in the absence of overt microcephaly.

Indexed as

Disease Models, AnimalMyelin SheathOligodendrogliaZika VirusZika Virus InfectionAnimalsBrainFemaleHumansMacaca nemestrinaMyelin Basic ProteinPregnancyPregnancy Complications, InfectiousMyelin Basic Protein

Identifiers

PMID38890352
PMCPMC11189406

What OpenQuestion holds

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Registered trials

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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.