Middle East Respiratory Syndrome Coronavirus Efficiently Infects Human Primary T Lymphocytes and Activates the Extrinsic and Intrinsic Apoptosis Pathways

Hin Chu(Biology of Infection), Jie Zhou(Biology of Infection), Bosco Ho‐Yin Wong, Cun Li, Jasper Fuk‐Woo Chan(Biology of Infection), Zhongshan Cheng, Dong Yang, Dong Wang, Andrew Chak-Yiu Lee, Chuangen Li, Man Lung Yeung(Biology of Infection), Jian‐Piao Cai, Ivy Hau-Yee Chan(University of Hong Kong), Wai‐Kuen Ho(University of Hong Kong), Kelvin Kai‐Wang To(Biology of Infection), Bo‐Jian Zheng(Biology of Infection), Yanfeng Yao(Academy of Medical Sciences), Chuan Qin(Institute of Laboratory Animal Science), Kwok‐Yung Yuen(Biology of Infection)
The Journal of Infectious Diseases
July 22, 2015
Cited by 472Open Access
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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.


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