Early Immune Responses to SARS Coronavirus in Ferrets

• Main Author: Danesh, Abdolali
• Other Authors: Kelvin, David J.
• Language: en_ca
• Published: 2012
• Subjects: Immunology; Infectious diseases; SARS; Ferret; Chemokines; Interferon; 0982
• Online Access: http://hdl.handle.net/1807/36278

Severe acute respiratory syndrome (SARS) was defined as an invasive respiratory disease in 2002, which originally came from China and rapidly spread all over the globe. Acute pneumonia and lower respiratory tract involvement most affected the middle aged individuals and elderly with a mortality rate of 11%. While SARS Corona virus (SARS-CoV) has maintained its potential capacity to reemerge, clinical study of the immune system of SARS patients, as well as controlled studies may lead to application of new treatment strategies in future. Throughout this work, I have focused on early immune responses to SARS-CoV in humans and in ferrets. CXCL0 has been associated with alterations in the clinical course of several infectious diseases, including SARS and influenza. Here I have cloned ferret CXCL10 gene and have expressed its recombinant protein. I demonstrate that the CXCL10 plasma level in SARS patients is associated with the severity of disease. I also show that endogenous ferret CXCL10 exhibits similar mRNA expression patterns in the lungs of deceased SARS patients and ferrets experimentally infected with SARS-CoV. Type I interferons (IFNs) are indispensable parts of the innate immunity during early stages of infection. A clear distinction between genes upregulated by direct virus-cell interactions and genes upregulated by secondary IFN production has not been made yet. Here, I have investigated differential gene regulation in ferrets upon subcutaneous administration of IFN-a2b and during SARS-CoV infection. In vivo experiments revealed that IFN-a2b causes upregulation of abundant IFN response genes (IRGs), chemokine receptors, and other genes that participate in phagocytosis and leukocyte migration. SARS-CoV infection of ferrets leads to upregulation of varieties of IRGs and a broad range of genes involved in cell migration and inflammation. This work allowed dissection of several molecular signatures present during SARS-CoV infection, which are part of a robust IFN antiviral response. Since localization of CD8+ Tcells may contribute to tissue injury, I have characterized ferret CD8 gene and have generated reagents that can be used in future studies with the aim of evaluating CD8+ T cells localization in the ferret lung during infection with SARS-CoV.