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SAS-Coronavirus: Diagnosis, Antibody Responses and Biosafty Conserns Cheng Cao Beijing Institute of Biotechnology, China
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2003 SARS Hit the World Outbroke in Guangdong Province in Nov, 2002 Hundreds Infected with >10% mortality including healthcare workers in 2 months Great terror spread all-over china Vinegar sold out in southern china (Anti-viral effect?) Spread to Beijing and Hong Kong Etiological agent not confirmed until early April It is the first time for China to fight against a communicable disease caused by unidentified pathogen
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>8000 Cases >700 Death
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Outbreak contained quickly by intensive public health measure (Identify patients and isolation) Accurate, fast methods for laboratory diagnosis are required Immunofluorescence Assay (IFA) RT-PCR Antibody Assay by ELISA using whole viral lysate as antigen Antibody Assay by ELISA using recombinant protein as antigen Antigen (N protein) assay by ELISA using Monoclonal antibody Only a few BSL-3 labs in China, no accreditation system
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Immunofluorenscene Assay Antibodies could be detected in 90% patients 15 days after infection No false positive found in 104 health sample (Indirect ELISA using viral lysate gave 2.9% false positive
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Recombinant Nucleocapsid protein is a good antigen in antibody assay Antigen for coating Antigen For HRP labeling All SARS-CoV encoded proteins are expressed in E.coli Antibodies against N protein could be detected in >80% sera from SARS patients An antigen-capturing ELISA developed in later April, 2003 and certified by SFDA soon No viral culture is needed in the process (Compared to IFA).
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Approaches to develop highly sensitive and specific ELISA kit To reduce false positives, highly purified (>99%)protein was employed Proteins for coating and for labeling were purified by different methods to avoid cross reaction due to bacterial proteins. The Nucleocapsid protein was expressed as N ter and C ter for coating, to avoid self-aggregating and reduce background.
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Patient Type (days after illness) No. of samples No. of Positive % Probable SARS(0-5)24414.8 Probable SARS(6-10)382668.4 Probable SARS(10- 61) 13512189.6 No SARS fever4400 HCW8000 Healthy people94010.106 Serum in 2002180010.06 It seems that the nucleocapsid protein was not cross-reactive with antibodies against other coronavirus Subclinical SARS before outbroke?
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Antigen capturing Vs. Other antibody assays Sera samples from early phase patients
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Antibodies against nucleocapsid protein persisted for years
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Cao et al. 2005 Yasui, et al. 2008 The nucleocapsid was involved in Viral mediated inflammation
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The Nucleocapsid protein inhibits translation by interacting with EF1a
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The N protein inhibits cytokinesis and cell proliferation
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The N Protein interacts with Cyp4F3, the ω-hydroxylase of leukotriene B4
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The N Protein inhibits the ω-hydroxylation of leukotriene B4
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Expression of N protein resulted in accumulation of LTB4 and lung injury
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The N protein activates MASP2, a key protease in MBL complement pathway
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SARS-CoV N protein accelerate the C4 cleavage by MASP2
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SARS-CoV N protein play important role in complement activation C4 C5-9
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SARS: Biosceurity Concerns Reemergence of the disease SARS-CoV-like virus circulating within the Chinese horseshoe bat Similar SARS-CoV like virus were identified recently in horseshoe bats in Slovenia and leaf-nosed bats in Nigeria Laboratory risk 2004, 8 cases with 1 death due to laboratory leak in Beijing due to inadequate laboratory safety procedure LAIs have also been reported in laboratory workers in Singapore and Taiwan before
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SARS: Biosceurity Concerns Manipulation of SARS coronavirus and infected tissues MUST be done in BSL-3 labs Only well-trained scientists and technicians could be allowed to work with the virus in BSL-3 lab. Post- graduates in China should not be allowed. For serum tests, experiments could be done in BSL2 lab. All the sera from SARS patients have to be incubated at 56°C for 30min to inactivate the virus. Sampling should be done in biosafety cabinets.
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谢谢!
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