SARS CoV-2 Spike protein in silico interaction with ACE2 receptors from wild and domestic species

The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has been declared a pandemic by the World Health Organization (WHO) and since its first report it has become a major public health concern. SARS-CoV-2 is closely related to SARS-CoV and SARS-related bat coronaviruses and it has been de...

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Detalles Bibliográficos
Autores: Rendon Marin, Santiago, Martinez Gutierrez, Marlen, Whittaker, Gary, Jaimes, Javier Andres, Ruiz Saenz, Julian
Tipo de recurso: artículo
Fecha de publicación:2021
País:Colombia
Institución:Universidad Cooperativa de Colombia
Repositorio:Repositorio UCC
OAI Identifier:oai:https://repository.ucc.edu.co:20.500.12494/32931
Acceso en línea:http://hdl.handle.net/20.500.12494/32931
Access Level:acceso abierto
Palabra clave:SARS-CoV-2
COVID-19
Homology modeling
Molecular docking
Spike protein
Descripción
Sumario:The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has been declared a pandemic by the World Health Organization (WHO) and since its first report it has become a major public health concern. SARS-CoV-2 is closely related to SARS-CoV and SARS-related bat coronaviruses and it has been described to use angiotensin converting enzyme 2 (ACE2) as a receptor. Natural SARS-CoV-2 infection in domestic and wildlife animals, measured by RT-qPCR, has been confirmed in different countries, especially from the Felidae family. In silico analysis of the interaction between the SARS-CoV-2 spike protein and the cellular receptor ACE2 in various animal species have suggested that wild felids and domestic cats could be susceptible to SARS-CoV-2 based on this interaction. Here, we performed a protein-protein molecular docking analysis of SARS-CoV-2 spike protein with the ACE2 receptor from different animals to elucidate the potential of those species as intermediate hosts or susceptible animals for SARS-CoV-2 infection. Compared to human ACE2, we found that ACE2 receptors from domestic cats and tigers could efficiently interact with RBD of SARS CoV-2 Spike protein. However, dog, ferret, and hamster ACE2 receptor interaction with SARS-CoV-2 S protein RBD was not predicted as favorable, demonstrating a potential differentiated susceptibility in the evaluated species.