Severe acute respiratory syndrome (SARS) is the first new epidemic of the twenty-first century. A novel coronavirus (SARS-CoV) has been identified as the causative agent of SARS. The genome of SARS-CoV has 29,727 nucl...Severe acute respiratory syndrome (SARS) is the first new epidemic of the twenty-first century. A novel coronavirus (SARS-CoV) has been identified as the causative agent of SARS. The genome of SARS-CoV has 29,727 nucleatides in length. The genome organization, with 11 open reading frames, is similar to that of coronaviruses. Phylogenetic analyses and sequence comparisons showed that SARS-CoV is not closely related to any of the known coronaviruses, indicating neither a mutant nor recombinant of well-characterized coronaviruses. It is a complete new coronavirus from nonhuman host. Pathological studies show that severe immune response, associated to cytokine dysregulation, may be related to the lung damage of fatal SRAS. Recombination of genomes of wild-type strains with vaccine coronavirus is a potential risk associated with the application of living attenuated coronavirus vaccines. The proteinases, controlling the activities of the SARS-CoV replication, and spike protein, involved in viral entry and pathogenesis, represent attractive targets of anti-SARS drug development. Comparative full-length genome sequence analysis of 14 SARS coronavirus isolates suggests a remarkable genetic conservation of the virus. Anti-SARS vaccine and drug development will benefit from this genetic conservation. SARS-CoV is not likely to change rapidly and thus may not readily mutate to a benign infection. The progress in anti-SARS research has been impressive. However, one of the most effective tools in the control of the SARS is quickly tracing and isolating the contacts of stricken patients before they spread the virus further.展开更多
文摘Severe acute respiratory syndrome (SARS) is the first new epidemic of the twenty-first century. A novel coronavirus (SARS-CoV) has been identified as the causative agent of SARS. The genome of SARS-CoV has 29,727 nucleatides in length. The genome organization, with 11 open reading frames, is similar to that of coronaviruses. Phylogenetic analyses and sequence comparisons showed that SARS-CoV is not closely related to any of the known coronaviruses, indicating neither a mutant nor recombinant of well-characterized coronaviruses. It is a complete new coronavirus from nonhuman host. Pathological studies show that severe immune response, associated to cytokine dysregulation, may be related to the lung damage of fatal SRAS. Recombination of genomes of wild-type strains with vaccine coronavirus is a potential risk associated with the application of living attenuated coronavirus vaccines. The proteinases, controlling the activities of the SARS-CoV replication, and spike protein, involved in viral entry and pathogenesis, represent attractive targets of anti-SARS drug development. Comparative full-length genome sequence analysis of 14 SARS coronavirus isolates suggests a remarkable genetic conservation of the virus. Anti-SARS vaccine and drug development will benefit from this genetic conservation. SARS-CoV is not likely to change rapidly and thus may not readily mutate to a benign infection. The progress in anti-SARS research has been impressive. However, one of the most effective tools in the control of the SARS is quickly tracing and isolating the contacts of stricken patients before they spread the virus further.
