دورية أكاديمية

An Antiviral Role for TRIM14 in Ebola Virus Infection.

التفاصيل البيبلوغرافية
العنوان: An Antiviral Role for TRIM14 in Ebola Virus Infection.
المؤلفون: Kuroda M; Influenza Research Institute, Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, Madison, Wisconsin, USA., Halfmann PJ; Influenza Research Institute, Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, Madison, Wisconsin, USA., Thackray LB; Department of Medicine, Washington University School of Medicine, St Louis, Missouri, USA., Diamond MS; Department of Medicine, Washington University School of Medicine, St Louis, Missouri, USA.; Department of Pathology and Immunology, Washington University School of Medicine, St Louis, Missouri, USA.; Department of Molecular Microbiology, Washington University School of Medicine, St Louis, Missouri, USA.; The Andrew M. and Jane M. Bursky Center for Human Immunology and Immunotherapy Programs, Washington University School of Medicine, St Louis, Missouri, USA.; Center for Vaccines and Immunity to Microbial Pathogens, Washington University School of Medicine, St Louis, Missouri, USA., Feldmann H; Laboratory of Virology, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, Montana, USA., Marzi A; Laboratory of Virology, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, Montana, USA., Kawaoka Y; Influenza Research Institute, Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, Madison, Wisconsin, USA.; Division of Virology, Department of Microbiology and Immunology, Institute of Medical Science, University of Tokyo, Tokyo, Japan.; The Research Center for Global Viral Diseases, National Center for Global Health and Medicine Research Institute, Tokyo, Japan.; Pandemic Preparedness, Infection and Advanced Research Center, University of Tokyo, Tokyo, Japan.
المصدر: The Journal of infectious diseases [J Infect Dis] 2023 Nov 15; Vol. 228 (Suppl 7), pp. S514-S521.
نوع المنشور: Journal Article; Research Support, N.I.H., Extramural
اللغة: English
بيانات الدورية: Publisher: Oxford University Press Country of Publication: United States NLM ID: 0413675 Publication Model: Print Cited Medium: Internet ISSN: 1537-6613 (Electronic) Linking ISSN: 00221899 NLM ISO Abbreviation: J Infect Dis Subsets: MEDLINE
أسماء مطبوعة: Publication: Jan. 2011- : Oxford : Oxford University Press
Original Publication: 1904-2010 : Chicago, IL : University of Chicago Press
مواضيع طبية MeSH: Ebolavirus*/genetics , Hemorrhagic Fever, Ebola*, Animals ; Mice ; Interferon Type I/metabolism ; Viral Proteins/metabolism
مستخلص: Ebola virus (EBOV) is a highly pathogenic virus that encodes 7 multifunctional structural proteins. Multiple host factors have been reported to interact with the EBOV proteins. Here, we found that tripartite motif-containing 14 (TRIM14), an interferon-stimulated gene that mediates cellular signaling pathways associated with type I interferon and inflammatory cytokine production, interacts with EBOV nucleoprotein to enhance interferon-β (IFN-β) and nuclear factor-κB (NF-κB) promotor activation. Moreover, TRIM14 overexpression reduced viral replication in an infectious but biologically contained EBOVΔVP30 system by approximately 10-fold without affecting viral protein expression. Furthermore, TRM14-deficient mice were more susceptible to mouse-adapted EBOV infection than wild-type mice. Our data suggest that TRIM14 is a host factor with anti-EBOV activity that limits EBOV pathogenesis.
Competing Interests: Potential conflicts of interest . Y.K. has received unrelated funding support from FUJIFILM Toyama Chemical Co. LTD, Shionogi & Co. LTD, Daiichi Sankyo Pharmaceutical, Otsuka Pharmaceutical, KM Biologics, Kyoritsu Seiyaku, Fuji Rebio, Tauns Laboratories, Inc., and FluGen.
(© The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.)
References: J Virol. 2007 Dec;81(24):13469-77. (PMID: 17928350)
Front Immunol. 2017 Jan 03;7:662. (PMID: 28096803)
J Virol. 2006 Jun;80(11):5168-78. (PMID: 16698997)
Nat Commun. 2020 Jun 11;11(1):2953. (PMID: 32528005)
Genes Immun. 2021 May;22(1):56-63. (PMID: 33864033)
Front Microbiol. 2019 Feb 26;10:344. (PMID: 30873142)
Nature. 2014 Jan 30;505(7485):691-5. (PMID: 24284630)
J Virol. 2006 Jun;80(11):5156-67. (PMID: 16698996)
Adv Sci (Weinh). 2019 Nov 11;7(1):1901261. (PMID: 31921549)
J Pathol. 2015 Jan;235(2):153-74. (PMID: 25297522)
J Virol. 2014 Nov;88(21):12500-10. (PMID: 25142601)
J Virol. 2020 Jul 30;94(16):. (PMID: 32493824)
Nat Rev Microbiol. 2015 Nov;13(11):663-76. (PMID: 26439085)
Proc Natl Acad Sci U S A. 2014 Jan 14;111(2):E245-54. (PMID: 24379373)
J Virol. 2010 Jan;84(2):1169-75. (PMID: 19889762)
Nature. 2018 Nov;563(7729):137-140. (PMID: 30333622)
J Virol. 2006 Apr;80(8):3743-51. (PMID: 16571791)
Cell Host Microbe. 2013 Jul 17;14(1):74-84. (PMID: 23870315)
Mol Cell. 2016 Oct 6;64(1):105-119. (PMID: 27666593)
Philos Trans R Soc Lond B Biol Sci. 2017 May 26;372(1721):. (PMID: 28396469)
Annu Rev Pathol. 2017 Jan 24;12:387-418. (PMID: 27959626)
PLoS Pathog. 2022 Jul 28;18(7):e1010616. (PMID: 35900983)
Cell Rep. 2018 May 8;23(6):1806-1816. (PMID: 29742435)
J Gen Virol. 2010 Feb;91(Pt 2):352-61. (PMID: 19828757)
Mol Cell. 2017 Oct 19;68(2):293-307.e5. (PMID: 29053956)
Sci Rep. 2016 Aug 31;6:32336. (PMID: 27578425)
Proc Natl Acad Sci U S A. 2008 Jan 29;105(4):1129-33. (PMID: 18212124)
Cell Mol Immunol. 2021 Mar;18(3):539-555. (PMID: 33462384)
Biochim Biophys Acta. 2014 Nov;1843(11):2754-2764. (PMID: 25116307)
J Infect Dis. 2018 Nov 22;218(suppl_5):S453-S457. (PMID: 29878128)
Nat Rev Immunol. 2008 Nov;8(11):849-60. (PMID: 18836477)
Front Immunol. 2018 Aug 13;9:1872. (PMID: 30150992)
معلومات مُعتمدة: U19 AI106772 United States AI NIAID NIH HHS; U19AI106772 United States NH NIH HHS
فهرسة مساهمة: Keywords: Ebola virus; NF-κB; TRIM14; interferon
المشرفين على المادة: 0 (Interferon Type I)
0 (Viral Proteins)
0 (Trim14 protein, mouse)
تواريخ الأحداث: Date Created: 20230810 Date Completed: 20231130 Latest Revision: 20240213
رمز التحديث: 20240213
مُعرف محوري في PubMed: PMC10651195
DOI: 10.1093/infdis/jiad325
PMID: 37562033
قاعدة البيانات: MEDLINE
الوصف
تدمد:1537-6613
DOI:10.1093/infdis/jiad325