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

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

2020Microorganisms23 citationsDOIOpen Access PDF

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.

Topics & Concepts

Peripheral blood mononuclear cellBiologyCoxsackievirusVirologyMessenger RNAEndogenous retrovirusMolecular biologyEnterovirusDownregulation and upregulationMonocyteCell cultureImmunologyVirusIn vitroGeneGenomeBiochemistryGeneticsViral Infections and Immunology ResearchViral gastroenteritis research and epidemiologyRNA and protein synthesis mechanisms
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