4.6 Article

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

Journal

MICROORGANISMS
Volume 8, Issue 9, Pages -

Publisher

MDPI
DOI: 10.3390/microorganisms8091335

Keywords

enterovirus; endogenous retrovirus; pancreatic cells; macrophages; PBMCs

Categories

Funding

  1. Laboratoire de Virologie ULR 3610, Universite de Lille et CHU de Lille
  2. Geneuro Innovation Lyon
  3. Universite de Lille
  4. Mobilex scholarship from the Universite de Lille

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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-WENVmRNA expression. Primary human pancreatic ductal cells were obtained from five brain-dead donors. In the pancreatic cells of three donors, the HERV-WENVmRNA 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-WENVmRNA level was higher than the background RNA level. In monocyte-derived macrophages obtained from 5 of 13 donors, the HERV-WENVmRNA 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-WENVcopy (or copies) in primary cell cultures, such as monocytes, macrophages, and pancreatic cells.

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