This study investigates the immune response of dogs to vaccination using cryo-electron microscopy and computational methods. The results reveal a specific polyclonal immune response in the serum of dogs infected with canine parvovirus and provide insights into the binding of multiple antibodies or ligands to the virus.
Canine parvovirus (CPV) is an important pathogen that emerged by cross-species transmission to cause severe disease in dogs. To understand the host immune response to vaccination, sera from dogs immunized with parvovirus are obtained, the polyclonal antibodies are purified and used to solve the high resolution cryo EM structures of the polyclonal Fab-virus complexes. We use a custom software, Icosahedral Subparticle Extraction and Correlated Classification (ISECC) to perform subparticle analysis and reconstruct polyclonal Fab-virus complexes from two different dogs eight and twelve weeks post vaccination. In the resulting polyclonal Fab-virus complexes there are a total of five distinct Fabs identified. In both cases, any of the five antibodies identified would interfere with receptor binding. This polyclonal mapping approach identifies a specific, limited immune response to the live vaccine virus and allows us to investigate the binding of multiple different antibodies or ligands to virus capsids. The polyclonal response from the serum of dogs infected with canine parvovirus is identified using cryo EM and a computational method to map the harvested Fab onto an icosahedral capsid.
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