Abstract
Middle East respiratory syndrome (MERS) is associated with a mortality rate of >35%. We previously showed that MERS coronavirus (MERS-CoV) could infect human macrophages and dendritic cells and induce cytokine dysregulation. Here, we further investigated the interplay between human primary T cells and MERS-CoV in disease pathogenesis. Importantly, our results suggested that MERS-CoV efficiently infected T cells from the peripheral blood and from human lymphoid organs, including the spleen and the tonsil. We further demonstrated that MERS-CoV infection induced apoptosis in T cells, which involved the activation of both the extrinsic and intrinsic apoptosis pathways. Remarkably, immunostaining of spleen sections from MERS-CoV-infected common marmosets demonstrated the presence of viral nucleoprotein in their CD3+ T cells. Overall, our results suggested that the unusual capacity of MERS-CoV to infect T cells and induce apoptosis might partly contribute to the high pathogenicity of the virus.
Original language | English |
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Pages (from-to) | 904-914 |
Number of pages | 11 |
Journal | Journal of Infectious Diseases |
Volume | 213 |
Issue number | 6 |
DOIs | |
Publication status | Published - Mar 15 2016 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2015 The Author. All rights reserved.
ASJC Scopus Subject Areas
- General Medicine
Keywords
- MERS-CoV
- T lymphocytes
- apoptosis
- caspase
- marmosets
- spleen
- tonsil