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  1. Article ; Online: Evaluation of two inoculation routes of an adenovirus-mediated viral protein inhibitor in a Crimean-Congo hemorrhagic fever mouse model.

    Scholte, Florine E M / Spengler, Jessica R / Welch, Stephen R / Harmon, Jessica R / Coleman-McCray, JoAnn D / Davies, Katherine A / Pegan, Scott D / Montgomery, Joel M / Spiropoulou, Christina F / Bergeron, Éric

    Virus research

    2024  , Page(s) 199398

    Abstract: ... such as CC4 is their requirement for intracellular delivery, e.g., by viral vectors. In this study ...

    Abstract Crimean-Congo hemorrhagic fever virus (CCHFV) is a tick-borne nairovirus with a wide geographic spread that can cause severe and lethal disease. No specific medical countermeasures are approved to combat this illness. The CCHFV L protein contains an ovarian tumor OTU domain with a cysteine protease thought to modulate cellular immune responses by removing ubiquitin and ISG15 post-translational modifications from host and viral proteins. Viral deubiquitinases like CCHFV OTU are attractive drug targets, as blocking their activity may enhance cellular immune responses to infection, and potentially inhibit viral replication itself. We previously demonstrated that the engineered ubiquitin variant CC4 is a potent inhibitor of CCHFV replication in vitro. A major challenge of the therapeutic use of small protein inhibitors such as CC4 is their requirement for intracellular delivery, e.g., by viral vectors. In this study, we examined the feasibility of in vivo CC4 delivery by a replication-deficient recombinant adenovirus (Ad-CC4) in a lethal CCHFV mouse model. Since the liver is a primary target of CCHFV infection, we aimed to optimize delivery to this organ by comparing intravenous (tail vein) and intraperitoneal injection of Ad-CC4. While tail vein injection is a traditional route for adenovirus delivery, in our hands intraperitoneal injection resulted in higher and more widespread levels of adenovirus genome in tissues, including, as intended, the liver. However, despite promising in vitro results, neither route of in vivo CC4 treatment resulted in protection from a lethal CCHFV infection.
    Language English
    Publishing date 2024-05-14
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 605780-9
    ISSN 1872-7492 ; 0168-1702
    ISSN (online) 1872-7492
    ISSN 0168-1702
    DOI 10.1016/j.virusres.2024.199398
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: How ISG15 combats viral infection.

    Freitas, Brendan T / Scholte, Florine E M / Bergeron, Éric / Pegan, Scott D

    Virus research

    2020  Volume 286, Page(s) 198036

    Abstract: Interferon (IFN)-stimulated gene product 15 (ISG15) is a ubiquitin-like protein critical for the control of microbial infections. ISG15 appears to serve a wide variety of functions, which regulate multiple cellular responses contributing to the ... ...

    Abstract Interferon (IFN)-stimulated gene product 15 (ISG15) is a ubiquitin-like protein critical for the control of microbial infections. ISG15 appears to serve a wide variety of functions, which regulate multiple cellular responses contributing to the development of an antiviral state. ISG15 is a versatile molecule directly modulating both host and virus protein function which regulate many signaling pathways, including its own synthesis. Here we review the various roles ISG15 plays in the antiviral immune response, and examine the mechanisms by which viruses attempt to mitigate or exploit ISG15 activity.
    MeSH term(s) Animals ; Cytokines/genetics ; Cytokines/metabolism ; Humans ; Immunity, Innate/immunology ; Interferon Type I/immunology ; Macrophages/immunology ; Mice ; Neutrophils/immunology ; Signal Transduction/genetics ; Signal Transduction/immunology ; Ubiquitins/genetics ; Ubiquitins/metabolism ; Viral Proteins/metabolism ; Virus Diseases/immunology ; Virus Internalization ; Virus Replication/immunology
    Chemical Substances Cytokines ; Interferon Type I ; Ubiquitins ; Viral Proteins ; ISG15 protein, human (60267-61-0)
    Keywords covid19
    Language English
    Publishing date 2020-05-31
    Publishing country Netherlands
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Review
    ZDB-ID 605780-9
    ISSN 1872-7492 ; 0168-1702
    ISSN (online) 1872-7492
    ISSN 0168-1702
    DOI 10.1016/j.virusres.2020.198036
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Exploring inactivation of SARS-CoV-2, MERS-CoV, Ebola, Lassa, and Nipah viruses on N95 and KN95 respirator material using photoactivated methylene blue to enable reuse.

    Scholte, Florine E M / Kabra, Kareem B / Tritsch, Sarah R / Montgomery, Joel M / Spiropoulou, Christina F / Mores, Christopher N / Harcourt, Brian H

    American journal of infection control

    2022  Volume 50, Issue 8, Page(s) 863–870

    Abstract: Background: The COVID-19 pandemic resulted in a worldwide shortage of N95 respirators, prompting the development of decontamination methods to enable limited reuse. Countries lacking reliable supply chains would also benefit from the ability to safely ... ...

    Abstract Background: The COVID-19 pandemic resulted in a worldwide shortage of N95 respirators, prompting the development of decontamination methods to enable limited reuse. Countries lacking reliable supply chains would also benefit from the ability to safely reuse PPE. Methylene blue (MB) is a light-activated dye with demonstrated antimicrobial activity used to sterilize blood plasma. Decontamination of respirators using photoactivated MB requires no specialized equipment, making it attractive for use in the field during outbreaks.
    Methods: We examined decontamination of N95 and KN95 respirators using photoactivated MB and 3 variants of SARS-CoV-2, the virus that causes COVID-19; and 4 World Health Organization priority pathogens: Ebola virus, Middle East respiratory syndrome coronavirus, Nipah virus, and Lassa virus. Virus inactivation by pretreating respirator material was also tested.
    Results: Photoactivated MB inactivated all tested viruses on respirator material, albeit with varying efficiency. Virus applied to respirator material pre-treated with MB was also inactivated, thus MB pretreatment may potentially protect respirator wearers from virus exposure in real-time.
    Conclusions: These results demonstrate that photoactivated MB represents a cost-effective, rapid, and widely deployable method to decontaminate N95 respirators for reuse during supply shortages.
    MeSH term(s) COVID-19/prevention & control ; Decontamination/methods ; Equipment Reuse ; Hemorrhagic Fever, Ebola/prevention & control ; Humans ; Methylene Blue/pharmacology ; Middle East Respiratory Syndrome Coronavirus ; N95 Respirators ; Nipah Virus ; Pandemics/prevention & control ; SARS-CoV-2 ; Ventilators, Mechanical
    Chemical Substances Methylene Blue (T42P99266K)
    Language English
    Publishing date 2022-07-28
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 392362-9
    ISSN 1527-3296 ; 0196-6553
    ISSN (online) 1527-3296
    ISSN 0196-6553
    DOI 10.1016/j.ajic.2022.02.016
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: The alphavirus nonstructural protein 2 NTPase induces a host translational shut-off through phosphorylation of eEF2 via cAMP-PKA-eEF2K signaling.

    Emmely E Treffers / Ali Tas / Florine E M Scholte / Arnoud H de Ru / Eric J Snijder / Peter A van Veelen / Martijn J van Hemert

    PLoS Pathogens, Vol 19, Iss 2, p e

    2023  Volume 1011179

    Abstract: Chikungunya virus (CHIKV) is a reemerging alphavirus. Since 2005, it has infected millions of people during outbreaks in Africa, Asia, and South/Central America. CHIKV replication depends on host cell factors at many levels and is expected to have a ... ...

    Abstract Chikungunya virus (CHIKV) is a reemerging alphavirus. Since 2005, it has infected millions of people during outbreaks in Africa, Asia, and South/Central America. CHIKV replication depends on host cell factors at many levels and is expected to have a profound effect on cellular physiology. To obtain more insight into host responses to infection, stable isotope labeling with amino acids in cell culture and liquid chromatography-tandem mass spectrometry were used to assess temporal changes in the cellular phosphoproteome during CHIKV infection. Among the ~3,000 unique phosphorylation sites analyzed, the largest change in phosphorylation status was measured on residue T56 of eukaryotic elongation factor 2 (eEF2), which showed a >50-fold increase at 8 and 12 h p.i. Infection with other alphaviruses (Semliki Forest, Sindbis and Venezuelan equine encephalitis virus (VEEV)) triggered a similarly strong eEF2 phosphorylation. Expression of a truncated form of CHIKV or VEEV nsP2, containing only the N-terminal and NTPase/helicase domains (nsP2-NTD-Hel), sufficed to induce eEF2 phosphorylation, which could be prevented by mutating key residues in the Walker A and B motifs of the NTPase domain. Alphavirus infection or expression of nsP2-NTD-Hel resulted in decreased cellular ATP levels and increased cAMP levels. This did not occur when catalytically inactive NTPase mutants were expressed. The wild-type nsP2-NTD-Hel inhibited cellular translation independent of the C-terminal nsP2 domain, which was previously implicated in directing the virus-induced host shut-off for Old World alphaviruses. We hypothesize that the alphavirus NTPase activates a cellular adenylyl cyclase resulting in increased cAMP levels, thus activating PKA and subsequently eukaryotic elongation factor 2 kinase. This in turn triggers eEF2 phosphorylation and translational inhibition. We conclude that the nsP2-driven increase of cAMP levels contributes to the alphavirus-induced shut-off of cellular protein synthesis that is shared between Old and New World ...
    Keywords Immunologic diseases. Allergy ; RC581-607 ; Biology (General) ; QH301-705.5
    Subject code 572
    Language English
    Publishing date 2023-02-01T00:00:00Z
    Publisher Public Library of Science (PLoS)
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  5. Article ; Online: ISG15: It's Complicated.

    Dzimianski, John V / Scholte, Florine E M / Bergeron, Éric / Pegan, Scott D

    Journal of molecular biology

    2019  Volume 431, Issue 21, Page(s) 4203–4216

    Abstract: Interferon-stimulated gene product 15 (ISG15) is a key component of host responses to microbial infection. Despite having been known for four decades, grasping the functions and features of ISG15 has been a slow and elusive process. Substantial work over ...

    Abstract Interferon-stimulated gene product 15 (ISG15) is a key component of host responses to microbial infection. Despite having been known for four decades, grasping the functions and features of ISG15 has been a slow and elusive process. Substantial work over the past two decades has greatly enhanced this understanding, revealing the complex and variable nature of this protein. This has unveiled multiple mechanisms of action that are only now beginning to be understood. In addition, it has uncovered diversity not only between how ISG15 affects different pathogens but also between the function and structure of ISG15 itself between different host species. Here we review the complexity of ISG15 within the context of viral infection, focusing primarily on its antiviral function and the mechanisms viruses employ to thwart its effects. We highlight what is known regarding the impact of ISG15 sequence and structural diversity on these interactions and discuss the aspects presenting the next frontier toward elucidating a more complete picture of ISG15 function.
    MeSH term(s) Animals ; Cytokines/chemistry ; Cytokines/genetics ; Cytokines/metabolism ; Deubiquitinating Enzymes/genetics ; Deubiquitinating Enzymes/metabolism ; Humans ; Protein Structure, Secondary ; Ubiquitin Thiolesterase/chemistry ; Ubiquitin Thiolesterase/genetics ; Ubiquitin Thiolesterase/metabolism ; Ubiquitins/chemistry ; Ubiquitins/genetics ; Ubiquitins/metabolism ; Virus Diseases/metabolism
    Chemical Substances Cytokines ; Ubiquitins ; ISG15 protein, human (60267-61-0) ; Deubiquitinating Enzymes (EC 3.4.19.12) ; USP18 protein, human (EC 3.4.19.12) ; Ubiquitin Thiolesterase (EC 3.4.19.12)
    Keywords covid19
    Language English
    Publishing date 2019-03-16
    Publishing country Netherlands
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Review
    ZDB-ID 80229-3
    ISSN 1089-8638 ; 0022-2836
    ISSN (online) 1089-8638
    ISSN 0022-2836
    DOI 10.1016/j.jmb.2019.03.013
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Characterization of humoral responses to Nipah virus infection in the Syrian Hamster model of disease.

    Scholte, Florine E M / Rodriguez, Sergio E / Welch, Stephen R / Davies, Katherine A / Genzer, Sarah C / Coleman-McCray, JoAnn D / Harmon, Jessica R / Sorvillo, Teresa E / Lo, Michael K / Karaaslan, Elif / Bergeron, Eric / Montgomery, Joel M / Spengler, Jessica R / Spiropoulou, Christina F

    The Journal of infectious diseases

    2023  

    Abstract: Nipah virus (NiV) is a highly pathogenic paramyxovirus. The Syrian hamster model recapitulates key features of human NiV disease and is a critical tool for evaluating antivirals and vaccines. Here we describe longitudinal humoral immune responses in NiV- ... ...

    Abstract Nipah virus (NiV) is a highly pathogenic paramyxovirus. The Syrian hamster model recapitulates key features of human NiV disease and is a critical tool for evaluating antivirals and vaccines. Here we describe longitudinal humoral immune responses in NiV-infected Syrian hamsters. Samples were obtained 1-28 days after infection and analyzed by ELISA, neutralization, and Fc-mediated effector function assays. NiV infection elicited robust antibody responses against the nucleoprotein and attachment glycoprotein. Levels of neutralizing antibodies were modest and only detectable in surviving animals. Fc-mediated effector functions were mostly observed in nucleoprotein-targeting antibodies. Antibody levels and activities positively correlated with challenge dose.
    Language English
    Publishing date 2023-12-08
    Publishing country United States
    Document type Journal Article
    ZDB-ID 3019-3
    ISSN 1537-6613 ; 0022-1899
    ISSN (online) 1537-6613
    ISSN 0022-1899
    DOI 10.1093/infdis/jiad557
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: The alphavirus nonstructural protein 2 NTPase induces a host translational shut-off through phosphorylation of eEF2 via cAMP-PKA-eEF2K signaling.

    Treffers, Emmely E / Tas, Ali / Scholte, Florine E M / de Ru, Arnoud H / Snijder, Eric J / van Veelen, Peter A / van Hemert, Martijn J

    PLoS pathogens

    2023  Volume 19, Issue 2, Page(s) e1011179

    Abstract: Chikungunya virus (CHIKV) is a reemerging alphavirus. Since 2005, it has infected millions of people during outbreaks in Africa, Asia, and South/Central America. CHIKV replication depends on host cell factors at many levels and is expected to have a ... ...

    Abstract Chikungunya virus (CHIKV) is a reemerging alphavirus. Since 2005, it has infected millions of people during outbreaks in Africa, Asia, and South/Central America. CHIKV replication depends on host cell factors at many levels and is expected to have a profound effect on cellular physiology. To obtain more insight into host responses to infection, stable isotope labeling with amino acids in cell culture and liquid chromatography-tandem mass spectrometry were used to assess temporal changes in the cellular phosphoproteome during CHIKV infection. Among the ~3,000 unique phosphorylation sites analyzed, the largest change in phosphorylation status was measured on residue T56 of eukaryotic elongation factor 2 (eEF2), which showed a >50-fold increase at 8 and 12 h p.i. Infection with other alphaviruses (Semliki Forest, Sindbis and Venezuelan equine encephalitis virus (VEEV)) triggered a similarly strong eEF2 phosphorylation. Expression of a truncated form of CHIKV or VEEV nsP2, containing only the N-terminal and NTPase/helicase domains (nsP2-NTD-Hel), sufficed to induce eEF2 phosphorylation, which could be prevented by mutating key residues in the Walker A and B motifs of the NTPase domain. Alphavirus infection or expression of nsP2-NTD-Hel resulted in decreased cellular ATP levels and increased cAMP levels. This did not occur when catalytically inactive NTPase mutants were expressed. The wild-type nsP2-NTD-Hel inhibited cellular translation independent of the C-terminal nsP2 domain, which was previously implicated in directing the virus-induced host shut-off for Old World alphaviruses. We hypothesize that the alphavirus NTPase activates a cellular adenylyl cyclase resulting in increased cAMP levels, thus activating PKA and subsequently eukaryotic elongation factor 2 kinase. This in turn triggers eEF2 phosphorylation and translational inhibition. We conclude that the nsP2-driven increase of cAMP levels contributes to the alphavirus-induced shut-off of cellular protein synthesis that is shared between Old and New World alphaviruses. MS Data are available via ProteomeXchange with identifier PXD009381.
    MeSH term(s) Humans ; Alphavirus/metabolism ; Nucleoside-Triphosphatase/metabolism ; Peptide Elongation Factor 2/metabolism ; Eukaryota ; Phosphorylation ; Chikungunya virus/physiology ; Chikungunya Fever ; Viral Nonstructural Proteins/metabolism ; Virus Replication ; Elongation Factor 2 Kinase/metabolism
    Chemical Substances Nucleoside-Triphosphatase (EC 3.6.1.15) ; Peptide Elongation Factor 2 ; Viral Nonstructural Proteins ; EEF2K protein, human (EC 2.7.1.17) ; Elongation Factor 2 Kinase (EC 2.7.11.20)
    Language English
    Publishing date 2023-02-27
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2205412-1
    ISSN 1553-7374 ; 1553-7374
    ISSN (online) 1553-7374
    ISSN 1553-7374
    DOI 10.1371/journal.ppat.1011179
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article: How ISG15 combats viral infection

    Freitas, Brendan T / Scholte, Florine E.M / Bergeron, Éric / Pegan, Scott D

    Elsevier B.V. Virus research. 2020 Sept., v. 286

    2020  

    Abstract: Interferon (IFN)-stimulated gene product 15 (ISG15) is a ubiquitin-like protein critical for the control of microbial infections. ISG15 appears to serve a wide variety of functions, which regulate multiple cellular responses contributing to the ... ...

    Abstract Interferon (IFN)-stimulated gene product 15 (ISG15) is a ubiquitin-like protein critical for the control of microbial infections. ISG15 appears to serve a wide variety of functions, which regulate multiple cellular responses contributing to the development of an antiviral state. ISG15 is a versatile molecule directly modulating both host and virus protein function which regulate many signaling pathways, including its own synthesis. Here we review the various roles ISG15 plays in the antiviral immune response, and examine the mechanisms by which viruses attempt to mitigate or exploit ISG15 activity.
    Keywords genes ; immune response ; interferons ; signal transduction ; viral proteins ; viruses
    Language English
    Dates of publication 2020-09
    Publishing place Elsevier B.V.
    Document type Article
    ZDB-ID 605780-9
    ISSN 1872-7492 ; 0168-1702
    ISSN (online) 1872-7492
    ISSN 0168-1702
    DOI 10.1016/j.virusres.2020.198036
    Database NAL-Catalogue (AGRICOLA)

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  9. Article ; Online: Defective Interfering Viral Particle Treatment Reduces Clinical Signs and Protects Hamsters from Lethal Nipah Virus Disease.

    Welch, Stephen R / Spengler, Jessica R / Harmon, Jessica R / Coleman-McCray, JoAnn D / Scholte, Florine E M / Genzer, Sarah C / Lo, Michael K / Montgomery, Joel M / Nichol, Stuart T / Spiropoulou, Christina F

    mBio

    2022  Volume 13, Issue 2, Page(s) e0329421

    Abstract: Defective interfering particles (DIs) contain a considerably smaller genome than the parental virus but retain replication competency. As DIs can directly or indirectly alter propagation kinetics of the parental virus, they offer a novel approach to ... ...

    Abstract Defective interfering particles (DIs) contain a considerably smaller genome than the parental virus but retain replication competency. As DIs can directly or indirectly alter propagation kinetics of the parental virus, they offer a novel approach to antiviral therapy, capitalizing on knowledge from natural infection. However, efforts to translate
    MeSH term(s) Animals ; Cricetinae ; Disease Models, Animal ; Henipavirus Infections/prevention & control ; Mesocricetus ; Nipah Virus ; Virion
    Language English
    Publishing date 2022-03-17
    Publishing country United States
    Document type Journal Article ; Research Support, U.S. Gov't, P.H.S.
    ZDB-ID 2557172-2
    ISSN 2150-7511 ; 2161-2129
    ISSN (online) 2150-7511
    ISSN 2161-2129
    DOI 10.1128/mbio.03294-21
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article: How ISG15 combats viral infection

    Freitas, Brendan T / Scholte, Florine E M / Bergeron, Éric / Pegan, Scott D

    Virus Res

    Abstract: Interferon (IFN)-stimulated gene product 15 (ISG15) is a ubiquitin-like protein critical for the control of microbial infections. ISG15 appears to serve a wide variety of functions, which regulate multiple cellular responses contributing to the ... ...

    Abstract Interferon (IFN)-stimulated gene product 15 (ISG15) is a ubiquitin-like protein critical for the control of microbial infections. ISG15 appears to serve a wide variety of functions, which regulate multiple cellular responses contributing to the development of an antiviral state. ISG15 is a versatile molecule directly modulating both host and virus protein function which regulate many signaling pathways, including its own synthesis. Here we review the various roles ISG15 plays in the antiviral immune response, and examine the mechanisms by which viruses attempt to mitigate or exploit ISG15 activity.
    Keywords covid19
    Publisher WHO
    Document type Article
    Note WHO #Covidence: #625038
    Database COVID19

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