Middle East respiratory syndrome coronavirus shows poor replication but significant induction of antiviral responses in human monocyte-derived macrophages and dendritic cells

J Gen Virol. 2016 Feb;97(2):344-355. doi: 10.1099/jgv.0.000351. Epub 2015 Nov 24.

Abstract

In this study we assessed the ability of Middle East respiratory syndrome coronavirus (MERS-CoV) to replicate and induce innate immunity in human monocyte-derived macrophages and dendritic cells (MDDCs), and compared it with severe acute respiratory syndrome coronavirus (SARS-CoV). Assessments of viral protein and RNA levels in infected cells showed that both viruses were impaired in their ability to replicate in these cells. Some induction of IFN-λ1, CXCL10 and MxA mRNAs in both macrophages and MDDCs was seen in response to MERS-CoV infection, but almost no such induction was observed in response to SARS-CoV infection. ELISA and Western blot assays showed clear production of CXCL10 and MxA in MERS-CoV-infected macrophages and MDDCs. Our data suggest that SARS-CoV and MERS-CoV replicate poorly in human macrophages and MDDCs, but MERS-CoV is nonetheless capable of inducing a readily detectable host innate immune response. Our results highlight a clear difference between the viruses in activating host innate immune responses in macrophages and MDDCs, which may contribute to the pathogenesis of infection.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Chemokine CXCL10 / metabolism
  • Dendritic Cells / immunology*
  • Dendritic Cells / virology*
  • Humans
  • Immunity, Innate
  • Macrophages / immunology*
  • Macrophages / virology*
  • Middle East Respiratory Syndrome Coronavirus / immunology*
  • Middle East Respiratory Syndrome Coronavirus / physiology*
  • Myxovirus Resistance Proteins / metabolism
  • RNA, Viral / analysis
  • Severe acute respiratory syndrome-related coronavirus / immunology
  • Severe acute respiratory syndrome-related coronavirus / physiology
  • Viral Proteins / analysis
  • Virus Replication*

Substances

  • CXCL10 protein, human
  • Chemokine CXCL10
  • MX1 protein, human
  • Myxovirus Resistance Proteins
  • RNA, Viral
  • Viral Proteins