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Artikel: Fluoxetine Can Inhibit SARS-CoV-2 In Vitro

Dechaumes, Arthur / Nekoua, Magloire Pandoua / Belouzard, Sandrine / Sane, Famara / Engelmann, Ilka / Dubuisson, Jean / Alidjinou, Enagnon Kazali / Hober, Didier

Microorganisms. 2021 Feb. 09, v. 9, no. 2

2021

Abstract: An outbreak of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) resulted in the coronavirus disease pandemic, drastically affecting global health and economy. Though the understanding of the disease has improved, fighting the virus remains ... ...

Abstract	An outbreak of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) resulted in the coronavirus disease pandemic, drastically affecting global health and economy. Though the understanding of the disease has improved, fighting the virus remains challenging. One of the strategies is repurposing existing drugs as inhibitors of SARS-CoV-2. Fluoxetine (FLX), a selective serotonin reuptake inhibitor, reportedly inhibits the replication of RNA viruses, especially Coxsackieviruses B (CVB), such as CV-B4 in vitro and in vivo. Therefore, in this study, we investigated the in vitro antiviral activity of FLX against SARS-CoV-2 in a model of acute infection. When 10 μM of FLX was added to SARS-CoV-2-infected Vero E6 cells, the virus-induced cytopathic effect was not observed. In this model, the level of infectious particles in the supernatant was lower than that in controls. The level was below the limit of detection of the assay up to day 3 post-infection when FLX was administered before viral inoculation or simultaneously followed by daily inoculation. In conclusion, FLX can inhibit SARS-CoV-2 in vitro. Further studies are needed to investigate the potential value of FLX to combat SARS-CoV-2 infections, treat SARS-CoV-2-induced diseases, and explain the antiviral mechanism of this molecule to pave way for novel treatment strategies.
Schlagwörter	Enterovirus ; RNA ; Severe acute respiratory syndrome coronavirus 2 ; antiviral properties ; cytopathogenicity ; detection limit ; fluoxetine ; models ; pandemic ; serotonin ; viruses
Sprache	Englisch
Erscheinungsverlauf	2021-0209
Erscheinungsort	Multidisciplinary Digital Publishing Institute
Dokumenttyp	Artikel
ZDB-ID	2720891-6
ISSN	2076-2607
ISSN	2076-2607
DOI	10.3390/microorganisms9020339
Datenquelle	NAL Katalog (AGRICOLA)

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Artikel: Fluoxetine Can Inhibit SARS-CoV-2 In Vitro.

Dechaumes, Arthur / Nekoua, Magloire Pandoua / Belouzard, Sandrine / Sane, Famara / Engelmann, Ilka / Dubuisson, Jean / Alidjinou, Enagnon Kazali / Hober, Didier

Microorganisms

2021 Band 9, Heft 2

Abstract	An outbreak of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) resulted in the coronavirus disease pandemic, drastically affecting global health and economy. Though the understanding of the disease has improved, fighting the virus remains challenging. One of the strategies is repurposing existing drugs as inhibitors of SARS-CoV-2. Fluoxetine (FLX), a selective serotonin reuptake inhibitor, reportedly inhibits the replication of RNA viruses, especially Coxsackieviruses B (CVB), such as CV-B4 in vitro and in vivo. Therefore, in this study, we investigated the in vitro antiviral activity of FLX against SARS-CoV-2 in a model of acute infection. When 10 μM of FLX was added to SARS-CoV-2-infected Vero E6 cells, the virus-induced cytopathic effect was not observed. In this model, the level of infectious particles in the supernatant was lower than that in controls. The level was below the limit of detection of the assay up to day 3 post-infection when FLX was administered before viral inoculation or simultaneously followed by daily inoculation. In conclusion, FLX can inhibit SARS-CoV-2 in vitro. Further studies are needed to investigate the potential value of FLX to combat SARS-CoV-2 infections, treat SARS-CoV-2-induced diseases, and explain the antiviral mechanism of this molecule to pave way for novel treatment strategies.
Sprache	Englisch
Erscheinungsdatum	2021-02-09
Erscheinungsland	Switzerland
Dokumenttyp	Journal Article
ZDB-ID	2720891-6
ISSN	2076-2607
ISSN	2076-2607
DOI	10.3390/microorganisms9020339
Datenquelle	MEDical Literature Analysis and Retrieval System OnLINE

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Artikel: Enteroviral Pathogenesis of Type 1 Diabetes: The Role of Natural Killer Cells.

Nekoua, Magloire Pandoua / Dechaumes, Arthur / Sane, Famara / Alidjinou, Enagnon Kazali / Moutairou, Kabirou / Yessoufou, Akadiri / Hober, Didier

Microorganisms

2020 Band 8, Heft 7

Abstract: Enteroviruses, especially group B coxsackieviruses (CV-B), have been associated with the development of chronic diseases such as type 1 diabetes (T1D). The pathological mechanisms that trigger virus-induced autoimmunity against islet antigens in T1D are ... ...

Abstract	Enteroviruses, especially group B coxsackieviruses (CV-B), have been associated with the development of chronic diseases such as type 1 diabetes (T1D). The pathological mechanisms that trigger virus-induced autoimmunity against islet antigens in T1D are not fully elucidated. Animal and human studies suggest that NK cells response to CV-B infection play a crucial role in the enteroviral pathogenesis of T1D. Indeed, CV-B-infected cells can escape from cytotoxic T cells recognition and destruction by inhibition of cell surface expression of HLA class I antigen through non-structural viral proteins, but they can nevertheless be killed by NK cells. Cytolytic activity of NK cells towards pancreatic beta cells persistently-infected with CV-B has been reported and defective viral clearance by NK cells of patients with T1D has been suggested as a mechanism leading to persistence of CV-B and triggering autoimmunity reported in these patients. The knowledge about host antiviral defense against CV-B infection is not only crucial to understand the susceptibility to virus-induced T1D but could also contribute to the design of new preventive or therapeutic approaches for individuals at risk for T1D or newly diagnosed patients.
Sprache	Englisch
Erscheinungsdatum	2020-07-01
Erscheinungsland	Switzerland
Dokumenttyp	Journal Article ; Review
ZDB-ID	2720891-6
ISSN	2076-2607
ISSN	2076-2607
DOI	10.3390/microorganisms8070989
Datenquelle	MEDical Literature Analysis and Retrieval System OnLINE

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Artikel ; Online: Fluoxetine Can Inhibit SARS-CoV-2 In Vitro

Arthur Dechaumes / Magloire Pandoua Nekoua / Sandrine Belouzard / Famara Sane / Ilka Engelmann / Jean Dubuisson / Enagnon Kazali Alidjinou / Didier Hober

Microorganisms, Vol 9, Iss 2, p

2021 Band 339

Abstract	An outbreak of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) resulted in the coronavirus disease pandemic, drastically affecting global health and economy. Though the understanding of the disease has improved, fighting the virus remains challenging. One of the strategies is repurposing existing drugs as inhibitors of SARS-CoV-2. Fluoxetine (FLX), a selective serotonin reuptake inhibitor, reportedly inhibits the replication of RNA viruses, especially Coxsackieviruses B (CVB), such as CV-B4 in vitro and in vivo. Therefore, in this study, we investigated the in vitro antiviral activity of FLX against SARS-CoV-2 in a model of acute infection. When 10 μM of FLX was added to SARS-CoV-2-infected Vero E6 cells, the virus-induced cytopathic effect was not observed. In this model, the level of infectious particles in the supernatant was lower than that in controls. The level was below the limit of detection of the assay up to day 3 post-infection when FLX was administered before viral inoculation or simultaneously followed by daily inoculation. In conclusion, FLX can inhibit SARS-CoV-2 in vitro. Further studies are needed to investigate the potential value of FLX to combat SARS-CoV-2 infections, treat SARS-CoV-2-induced diseases, and explain the antiviral mechanism of this molecule to pave way for novel treatment strategies.
Schlagwörter	SARS-CoV-2 ; coronavirus ; fluoxetine ; in vitro ; Biology (General) ; QH301-705.5
Thema/Rubrik (Code)	570
Sprache	Englisch
Erscheinungsdatum	2021-02-01T00:00:00Z
Verlag	MDPI AG
Dokumenttyp	Artikel ; Online
Datenquelle	BASE - Bielefeld Academic Search Engine (Lebenswissenschaftliche Auswahl)

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Artikel: Desmin aggrephagy in rat and human ischemic heart failure through PKCζ and GSK3β as upstream signaling pathways.

Bouvet, Marion / Dubois-Deruy, Emilie / Turkieh, Annie / Mulder, Paul / Peugnet, Victoriane / Chwastyniak, Maggy / Beseme, Olivia / Dechaumes, Arthur / Amouyel, Philippe / Richard, Vincent / Lamblin, Nicolas / Pinet, Florence

Cell death discovery

2021 Band 7, Heft 1, Seite(n) 153

Abstract: Post-translational modifications of cardiac proteins could participate to left contractile dysfunction resulting in heart failure. Using a rat model of ischemic heart failure, we showed an accumulation of phosphorylated desmin leading to toxic aggregates ...

Abstract	Post-translational modifications of cardiac proteins could participate to left contractile dysfunction resulting in heart failure. Using a rat model of ischemic heart failure, we showed an accumulation of phosphorylated desmin leading to toxic aggregates in cardiomyocytes, but the cellular mechanisms are unknown. The same rat model was used to decipher the kinases involved in desmin phosphorylation and the proteolytic systems present in rat and human failing hearts. We used primary cultures of neonate rat cardiomyocytes for testing specific inhibitors of kinases and for characterizing the autophagic processes able to clear desmin aggregates. We found a significant increase of active PKCζ, no modulation of ubitiquitin-proteasome system, a defect in macroautophagy, and an activation of chaperone-mediated autophagy in heart failure rats. We validated in vitro that PKCζ inhibition induced a significant decrease of GSK3β and of soluble desmin. In vitro activation of ubiquitination of proteins and of chaperone-mediated autophagy is able to decrease soluble and insoluble forms of desmin in cardiomyocytes. These data demonstrate a novel signaling pathway implicating activation of PKCζ in desmin phosphorylation associated with a defect of proteolytic systems in ischemic heart failure, leading to desmin aggrephagy. Our in vitro data demonstrated that ubiquitination of proteins and chaperone-mediated autophagy are required for eliminating desmin aggregates with the contribution of its chaperone protein, α-crystallin Β-chain. Modulation of the kinases involved under pathological conditions may help preserving desmin intermediate filaments structure and thus protect the structural integrity of contractile apparatus of cardiomyocytes by limiting desmin aggregates formation.
Sprache	Englisch
Erscheinungsdatum	2021-06-26
Erscheinungsland	United States
Dokumenttyp	Journal Article
ISSN	2058-7716
ISSN	2058-7716
DOI	10.1038/s41420-021-00549-2
Datenquelle	MEDical Literature Analysis and Retrieval System OnLINE

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Artikel ; Online: Coxsackievirus-B4 Infection of Human Primary Pancreatic Ductal Cell Cultures Results in Impairment of Differentiation into Insulin-Producing Cells.

Bertin, Antoine / Sane, Famara / Gmyr, Valery / Lobert, Delphine / Dechaumes, Arthur / Kerr-Conte, Julie / Pattou, François / Hober, Didier

Viruses

2019 Band 11, Heft 7

Abstract: Coxsackievirus-B4 (CV-B4) E2 can persist in the pancreatic ductal-like cells (Panc-1 cell line), which results in an impaired differentiation of these cells into islet-like cell aggregates (ICA). In this study, primary pancreatic ductal cells obtained as ...

Abstract	Coxsackievirus-B4 (CV-B4) E2 can persist in the pancreatic ductal-like cells (Panc-1 cell line), which results in an impaired differentiation of these cells into islet-like cell aggregates (ICA). In this study, primary pancreatic ductal cells obtained as a by-product of islet isolation from the pancreas of seven brain-dead adults were inoculated with CV-B4 E2, followed-up for 29 days, and the impact was investigated. Viral titers in culture supernatants were analyzed throughout the culture. Intracellular viral RNA was detected by RT-PCR. Levels of ductal cell marker CK19 mRNA and of
Mesh-Begriff(e)	Cell Differentiation ; Cells, Cultured ; Coxsackievirus Infections/metabolism ; Coxsackievirus Infections/physiopathology ; Coxsackievirus Infections/virology ; Enterovirus B, Human/genetics ; Enterovirus B, Human/physiology ; Epithelial Cells ; Humans ; Insulin/metabolism ; Insulin-Secreting Cells/cytology ; Insulin-Secreting Cells/metabolism ; Pancreatic Ducts/virology
Chemische Substanzen	Insulin
Sprache	Englisch
Erscheinungsdatum	2019-07-02
Erscheinungsland	Switzerland
Dokumenttyp	Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID	2516098-9
ISSN	1999-4915 ; 1999-4915
ISSN (online)	1999-4915
ISSN	1999-4915
DOI	10.3390/v11070597
Datenquelle	MEDical Literature Analysis and Retrieval System OnLINE

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Artikel ; Online: Enteroviral Pathogenesis of Type 1 Diabetes

Magloire Pandoua Nekoua / Arthur Dechaumes / Famara Sane / Enagnon Kazali Alidjinou / Kabirou Moutairou / Akadiri Yessoufou / Didier Hober

Microorganisms, Vol 8, Iss 989, p

The Role of Natural Killer Cells

2020 Band 989

Abstract	Enteroviruses, especially group B coxsackieviruses (CV-B), have been associated with the development of chronic diseases such as type 1 diabetes (T1D). The pathological mechanisms that trigger virus-induced autoimmunity against islet antigens in T1D are not fully elucidated. Animal and human studies suggest that NK cells response to CV-B infection play a crucial role in the enteroviral pathogenesis of T1D. Indeed, CV-B-infected cells can escape from cytotoxic T cells recognition and destruction by inhibition of cell surface expression of HLA class I antigen through non-structural viral proteins, but they can nevertheless be killed by NK cells. Cytolytic activity of NK cells towards pancreatic beta cells persistently-infected with CV-B has been reported and defective viral clearance by NK cells of patients with T1D has been suggested as a mechanism leading to persistence of CV-B and triggering autoimmunity reported in these patients. The knowledge about host antiviral defense against CV-B infection is not only crucial to understand the susceptibility to virus-induced T1D but could also contribute to the design of new preventive or therapeutic approaches for individuals at risk for T1D or newly diagnosed patients.
Schlagwörter	enteroviruses ; NK cells ; HLA class I ; persistence ; type 1 diabetes ; Biology (General) ; QH301-705.5
Thema/Rubrik (Code)	610
Sprache	Englisch
Erscheinungsdatum	2020-07-01T00:00:00Z
Verlag	MDPI AG
Dokumenttyp	Artikel ; Online
Datenquelle	BASE - Bielefeld Academic Search Engine (Lebenswissenschaftliche Auswahl)

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Artikel: Coxsackievirus-B4 Infection Can Induce the Expression of Human Endogenous Retrovirus W in Primary Cells.

Dechaumes, Arthur / Bertin, Antoine / Sane, Famara / Levet, Sandrine / Varghese, Jennifer / Charvet, Benjamin / Gmyr, Valéry / Kerr-Conte, Julie / Pierquin, Justine / Arunkumar, Govindakarnavar / Pattou, François / Perron, Hervé / Hober, Didier

Microorganisms

2020 Band 8, Heft 9

Abstract: Human Endogenous Retrovirus W Envelope (HERV-W ENV) mRNA or protein can be found in peripheral blood mononuclear cells (PBMCs) and exocrine pancreas of patients with type 1 diabetes (T1D). Further, previous observations have shown an association between ... ...

Abstract	Human Endogenous Retrovirus W Envelope (HERV-W ENV) mRNA or protein can be found in peripheral blood mononuclear cells (PBMCs) and exocrine pancreas of patients with type 1 diabetes (T1D). Further, previous observations have shown an association between enteroviral infection and development of T1D; specifically, coxsackievirus-B (CV-B) has been detected in the blood and pancreas of patients with T1D. Notably, viruses can activate HERV-W expression. Hence, we evaluated the effect of CV-B4 infection on HERV-W
Sprache	Englisch
Erscheinungsdatum	2020-09-01
Erscheinungsland	Switzerland
Dokumenttyp	Journal Article
ZDB-ID	2720891-6
ISSN	2076-2607
ISSN	2076-2607
DOI	10.3390/microorganisms8091335
Datenquelle	MEDical Literature Analysis and Retrieval System OnLINE

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Artikel: Interplay Between Phosphorylation and O-GlcNAcylation of Sarcomeric Proteins in Ischemic Heart Failure.

Mercier, Thomas / Bouvet, Marion / Dubois-Deruy, Emilie / Dechaumes, Arthur / Beseme, Olivia / Richard, Vincent / Mulder, Paul / Pinet, Florence

Frontiers in endocrinology

2018 Band 9, Seite(n) 598

Abstract: Post-translational modifications (PTMs) of sarcomeric proteins could participate to left ventricular (LV) remodeling and contractile dysfunction leading in advanced heart failure (HF) with altered ejection fraction. Using an experimental rat model of HF ( ...

Abstract	Post-translational modifications (PTMs) of sarcomeric proteins could participate to left ventricular (LV) remodeling and contractile dysfunction leading in advanced heart failure (HF) with altered ejection fraction. Using an experimental rat model of HF (ligation of left coronary artery) and phosphoproteomic analysis, we identified an increase of desmin phosphorylation and a decrease of desmin O-N-acetylglucosaminylation (O-GlcNAcylation). We aim to characterize interplay between phosphorylation and O-GlcNAcylation for desmin in primary cultures of cardiomyocyte by specific O-GlcNAcase (OGA) inhibition with thiamet G and silencing O-GlcNAc transferase (OGT) and, in perfused heart perfused with thiamet G in sham- and HF-rats. In each model, we found an efficiency of O-GlcNAcylation modulation characterized by the levels of O-GlcNAcylated proteins and OGT expression (for silencing experiments in cells). In perfused heart, we found an improvement of cardiac function under OGA inhibition. But none of the treatments either in
Sprache	Englisch
Erscheinungsdatum	2018-10-05
Erscheinungsland	Switzerland
Dokumenttyp	Journal Article
ZDB-ID	2592084-4
ISSN	1664-2392
ISSN	1664-2392
DOI	10.3389/fendo.2018.00598
Datenquelle	MEDical Literature Analysis and Retrieval System OnLINE

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Artikel: Coxsackievirus-B4 Infection Can Induce the Expression of Human Endogenous Retrovirus W in Primary Cells

Microorganisms. 2020 Sept. 01, v. 8, no. 9

2020

Abstract	Human Endogenous Retrovirus W Envelope (HERV-W ENV) mRNA or protein can be found in peripheral blood mononuclear cells (PBMCs) and exocrine pancreas of patients with type 1 diabetes (T1D). Further, previous observations have shown an association between enteroviral infection and development of T1D; specifically, coxsackievirus-B (CV-B) has been detected in the blood and pancreas of patients with T1D. Notably, viruses can activate HERV-W expression. Hence, we evaluated the effect of CV-B4 infection on HERV-W ENV mRNA expression. Primary human pancreatic ductal cells were obtained from five brain-dead donors. In the pancreatic cells of three donors, the HERV-W ENV mRNA level measured using RT-qPCR was upregulated upon CV-B4 infection. The HERV-W ENV protein was detected in the infected cells using the immunoblot assay. In human PBMCs inoculated with CV-B4 or when CV-B4 was incubated with an enhancing serum, the HERV-W ENV mRNA level was higher than the background RNA level. In monocyte-derived macrophages obtained from 5 of 13 donors, the HERV-W ENV mRNA level was higher in cultures inoculated with CV-B4 than in the control. Therefore, CV-B4 can upregulate or induce the transcription of a certain HERV-W ENV copy (or copies) in primary cell cultures, such as monocytes, macrophages, and pancreatic cells.
Schlagwörter	Retroviridae ; blood serum ; gene expression ; humans ; insulin-dependent diabetes mellitus ; macrophages ; monocytes ; pancreas
Sprache	Englisch
Erscheinungsverlauf	2020-0901
Erscheinungsort	Multidisciplinary Digital Publishing Institute
Dokumenttyp	Artikel
ZDB-ID	2720891-6
ISSN	2076-2607
ISSN	2076-2607
DOI	10.3390/microorganisms8091335
Datenquelle	NAL Katalog (AGRICOLA)

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