Abstract
The ongoing COVID-19 pandemic in the world is caused by SARS-CoV-2, a new coronavirus first discovered in the end of 2019. It has led to more than 50 million confirmed cases and more than 1 million deaths across 219 countries by 11 November 2020, according to the WHO statistics. SARS-CoV-2, SARS-CoV, and MERS-CoV are alike. They are highly pathogenic, and they threaten public health, impair economy, and inflict long-term impacts on the society. No drug or vaccine has been approved as a cure for these viruses. The efforts to develop antiviral measures are hampered by the insufficient understanding of how the human body responds to viral infections at the cellular and molecular levels. In this study, journal articles and transcriptomic and proteomic data that survey coronavirus infections were collected. Response genes and proteins were then identified via differential analyses which compared the gene/protein between the infected sample and control. A database, H2V, was finally created for human genes/proteins responding to SARS-CoV-2, SARS-CoV, and MERS-CoV infection. H2V provides the molecular information about human response to infection. It can be a powerful tool to discover cellular pathways and processes relevant for viral pathogenesis to identify potential drug targets. It is expected to speed up the process of developing antiviral agents and to shed light on the preparation for potential coronavirus emergency in the future.