Key result
African swine fever virus entry involves multiple proteins and endocytic routes, providing novel therapeutic targets.
A comprehensive understanding of ASFV entry mechanisms provides a theoretical foundation for developing next-generation vaccines, antivirals, and disease-resistant pig populations.
Synthesizes ASFV multi-pathway entry data; leaves open in vivo validation of targets before guiding swine vaccine or antiviral development.
African swine fever (ASF), caused by the African swine fever virus (ASFV), remains one of the most devastating transboundary animal diseases worldwide, with case fatality rates reaching up to 100% in acute infections. Viral entry represents the first essential step in infection and is an ideal target for the development of vaccines and antiviral drugs. Recent studies have revealed that ASFV entry is not mediated by a single receptor or pathway. Instead, it involves multiple viral structural proteins, cellular attachment factors, endocytic routes, and intracellular trafficking regulators, which form a coordinated virus-host interaction network. In this review, we systematically summarize recent advances in ASFV multi-pathway invasion, including viral attachment, internalization, intracellular trafficking, uncoating, and membrane fusion. Additionally, we discuss several unresolved questions and highlight promising antiviral and genetic intervention strategies that target both viral components and host determinants. A comprehensive understanding of ASFV entry will provide the theoretical foundation for developing next-generation vaccines, antivirals, and disease-resistant pig populations.
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Li et al. (2026) conducted a review in African swine fever (ASF). African swine fever virus entry involves multiple viral structural proteins, cellular attachment factors, and endocytic routes, providing targets for next-generation vaccines and antivirals.
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