4.6 Article

Structural Insights into the Assembly of the African Swine Fever Virus Inner Capsid

Journal

JOURNAL OF VIROLOGY
Volume 97, Issue 6, Pages -

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/jvi.00268-23

Keywords

African swine fever virus; nucleocytoplasmic large DNA viruses; cryogenic electron microscopy; inner capsid assembly; new viral capsid scaffold; virion structure

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African swine fever virus (ASFV) is the cause of a highly contagious and fatal disease in domestic pigs. The structure of ASFV is complex, with multiple layers and proteins involved in assembly. The crystal structure of the major protein fragment p150(oNC) of ASFV has been determined, revealing a unique triangular-shaped plate structure. Further analysis showed that p150 or a similar protein in faustovirus assembles into hexameric and pentameric capsomeres, forming the icosahedral inner capsids. These findings provide new insights into the assembly of ASFV inner capsid and offer a basis for understanding the assembly of nucleocytoplasmic large DNA viruses (NCLDV).
African swine fever virus (ASFV), the cause of a highly contagious hemorrhagic and fatal disease of domestic pigs, has a complex multilayer structure. The inner capsid of ASFV located underneath the inner membrane enwraps the genome-containing nucleoid and is likely the assembly of proteolytic products from the virally encoded polyproteins pp220 and pp62. Here, we report the crystal structure of ASFV p150(oNC), a major middle fragment of the pp220 proteolytic product p150. The structure of ASFV p150(oNC) contains mainly helices and has a triangular plate-like shape. The triangular plate is approximately 38 angstrom in thickness, and the edge of the triangular plate is approximately 90 angstrom long. The structure of ASFV p150(oNC) is not homologous to any of the known viral capsid proteins. Further analysis of the cryo-electron microscopy maps of the ASFV and the homologous faustovirus inner capsids revealed that p150 or the p150-like protein of faustovirus assembles to form screwed propeller-shaped hexametric and pentametric capsomeres of the icosahedral inner capsids. Complexes of the C terminus of p150 and other proteolytic products of pp220 likely mediate interactions between the capsomeres. Together, these findings provide new insights into the assembling of ASFV inner capsid and provide a reference for understanding the assembly of the inner capsids of nucleocytoplasmic large DNA viruses (NCLDV).IMPORTANCE African swine fever virus has caused catastrophic destruction to the pork industry worldwide since it was first discovered in Kenya in 1921. The architecture of ASFV is complicated, with two protein shells and two membrane envelopes. Currently, mechanisms involved in the assembly of the ASFV inner core shell are less understood. The structural studies of the ASFV inner capsid protein p150 performed in this research enable the building of a partial model of the icosahedral ASFV inner capsid, which provides a structural basis for understanding the structure and assembly of this complex virion. Furthermore, the structure of ASFV p150(oNC) represents a new type of fold for viral capsid assembly, which could be a common fold for the inner capsid assembly of nucleocytoplasmic large DNA viruses (NCLDV) and would facilitate the development of vaccine and antivirus drugs against these complex viruses. African swine fever virus has caused catastrophic destruction to the pork industry worldwide since it was first discovered in Kenya in 1921. The architecture of ASFV is complicated, with two protein shells and two membrane envelopes.

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