The J. Craig Venter Institute (JCVI) has been involved in viral sequencing and analysis for more than 25 years, and coronavirus research for more than 15. This work has aided human health through vaccine development; improved food security by protecting crops and livestock; and provides critical data and analysis to researchers around the world. The Institute has also pioneered a synthetic biology platform which is now integral to fighting current and emerging viral threats.
Following is a summary of our various research projects on the novel coronavirus, SARS-CoV-2.
SARS-CoV-2 Research
COVID-19 Serology Testing
Informatics
JCVI is developing critical resources for the evaluation of antibody reactivity for serology testing. From an informatics perspective, the use of comparative genomics methods and predictive machine learning algorithms are being used to identify the key determinants for immune system recognition and to monitor the impact of virus evolution in immune system evasion. The bioinformatics analyses will aid in developing critical resources for the evaluation of antibody reactivity for serology testing.
Lab
In the laboratory, viral surface proteins are being generated for use as ELISA antigens, pseudotyped recombinant viruses are being constructed for neutralizing assays, and candidate vaccine constructs are being synthetized to define the immunogenicity of the viral proteins and to understand the basis of immune response and protection against SARS-CoV-2.
Funding
Funding for this research is provided through a variety of government and private sources.
We need your support now to continue and to expand upon these critical projects. If you would like to learn more about supporting any of this exciting research, please contact Jill Mullen at jmullen@jcvi.org.
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Coronavirus Support
Your support directly funds novel coronavirus research. This is monumental effort, requiring a wide range of scientific solutions. We need your support.
Virus pathogen database and analysis resource (ViPR): a comprehensive bioinformatics database and analysis resource for the coronavirus research community.
Genomic analysis of 16 Colorado human NL63 coronaviruses identifies a new genotype, high sequence diversity in the N-terminal domain of the spike gene and evidence of recombination.
The Journal of general virology. 2012-11-01; 93.Pt 11: 2387-2398.
Bovine-like coronaviruses isolated from four species of captive wild ruminants are homologous to bovine coronaviruses, based on complete genomic sequences.
Complete genomic sequences, a key residue in the spike protein and deletions in nonstructural protein 3b of US strains of the virulent and attenuated coronaviruses, transmissible gastroenteritis virus and porcine respiratory coronavirus.
Strategies to inhibit necrotic cell death or to prevent mitochondrial damage should be pursued as possible therapies to reduce cardiac damage during influenza infections
The research, which includes comparative genomics analysis by JCVI scientists Yun Zhang and Richard Scheuermann, provides essential information about the human immune response to coronavirus infection that will guide the design and evaluation of diagnostics and vaccine candidates