دورية أكاديمية

Entry receptor LDLRAD3 is required for Venezuelan equine encephalitis virus peripheral infection and neurotropism leading to pathogenesis in mice.

التفاصيل البيبلوغرافية
العنوان: Entry receptor LDLRAD3 is required for Venezuelan equine encephalitis virus peripheral infection and neurotropism leading to pathogenesis in mice.
المؤلفون: Kafai NM; Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA; Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA., Janova H; Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA., Cain MD; Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA., Alippe Y; Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA., Muraro S; Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA., Sariol A; Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA., Elam-Noll M; Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA., Klein RS; Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA; Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA; Department of Neuroscience, Washington University School of Medicine, St. Louis, MO 63110, USA., Diamond MS; Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA; Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA; Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO 63110, USA; The Andrew M. and Jane M. Bursky Center for Human Immunology and Immunotherapy Programs, Washington University School of Medicine, St. Louis, MO 63110, USA. Electronic address: mdiamond@wustl.edu.
المصدر: Cell reports [Cell Rep] 2023 Aug 29; Vol. 42 (8), pp. 112946. Date of Electronic Publication: 2023 Aug 08.
نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, Non-P.H.S.
اللغة: English
بيانات الدورية: Publisher: Cell Press Country of Publication: United States NLM ID: 101573691 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2211-1247 (Electronic) NLM ISO Abbreviation: Cell Rep Subsets: MEDLINE
أسماء مطبوعة: Original Publication: [Cambridge, MA] : Cell Press, c 2012-
مواضيع طبية MeSH: Encephalomyelitis, Venezuelan Equine*/pathology , Receptors, LDL*/physiology, Animals ; Mice ; Brain/pathology ; Central Nervous System ; Encephalitis Virus, Venezuelan Equine/physiology
مستخلص: Venezuelan equine encephalitis virus (VEEV) is an encephalitic alphavirus responsible for epidemics of neurological disease across the Americas. Low-density lipoprotein receptor class A domain-containing 3 (LDLRAD3) is a recently reported entry receptor for VEEV. Here, using wild-type and Ldlrad3-deficient mice, we define a critical role for LDLRAD3 in controlling steps in VEEV infection, pathogenesis, and neurotropism. Our analysis shows that LDLRAD3 is required for efficient VEEV infection and pathogenesis prior to and after central nervous system invasion. Ldlrad3-deficient mice survive intranasal and intracranial VEEV inoculation and show reduced infection of neurons in different brain regions. As LDLRAD3 is a determinant of pathogenesis and an entry receptor required for VEEV infection of neurons of the brain, receptor-targeted therapies may hold promise as countermeasures.
Competing Interests: Declaration of interests M.S.D. is a consultant for Inbios, Vir Biotechnology, Ocugen, Topspin Therapeutics, Moderna, and Immunome. The Diamond laboratory has received unrelated funding support in sponsored research agreements from Moderna, Vir Biotechnology, Generate Biomedicines, and Emergent BioSolutions.
(Copyright © 2023 The Author(s). Published by Elsevier Inc. All rights reserved.)
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معلومات مُعتمدة: F30 AI164842 United States AI NIAID NIH HHS; R01 AI014367 United States AI NIAID NIH HHS; R01 AI164653 United States AI NIAID NIH HHS; T32 AI007172 United States AI NIAID NIH HHS
فهرسة مساهمة: Keywords: CP: Microbiology; alphavirus, pathogenesis, receptor, tropism, brain, mice, animal model, infection, neuron
المشرفين على المادة: 0 (Receptors, LDL)
تواريخ الأحداث: Date Created: 20230809 Date Completed: 20230926 Latest Revision: 20240210
رمز التحديث: 20240210
مُعرف محوري في PubMed: PMC10529316
DOI: 10.1016/j.celrep.2023.112946
PMID: 37556325
قاعدة البيانات: MEDLINE
الوصف
تدمد:2211-1247
DOI:10.1016/j.celrep.2023.112946