Key result
High-dose ASFV-G-∆I177L produces no clinical signs or internal lesions of African swine fever in pigs.
Why the study?
It is critical to confirm the absence of any residual virulence in the ASFV vaccine candidate ASFV-G-∆I177L developed by genomic modification of parental virus strains.
Does ASFV-G-∆I177L exhibit residual virulence in domestic pigs?
Does ASFV-G-∆I177L exhibit residual virulence in domestic pigs?
Absolute Event Rate: 0% vs 0%
The ASFV-G-∆I177L vaccine candidate demonstrates long-term safety and lack of residual virulence in domestic pigs.
Gene-deleted live-attenuated ASF vaccines remain the leading approach; leaves open optimal targets and field efficacy in diverse swine populations.
African swine fever (ASF) is an important disease in swine currently producing a pandemic affecting pig production worldwide. Except in Vietnam, where two vaccines were recently approved for controlled use in the field, no vaccine is commercially available for disease control. Up to now, the most effective vaccines developed are based on the use of live-attenuated viruses. Most of these promising vaccine candidates were developed by deleting virus genes involved in the process of viral pathogenesis and disease production. Therefore, these vaccine candidates were developed via the genomic modification of parental virus field strains, producing recombinant viruses and reducing or eliminating their residual virulence. In this scenario, it is critical to confirm the absence of any residual virulence in the vaccine candidate. This report describes the assessment of the presence of residual virulence in the ASFV vaccine candidate ASFV-G-∆I177L in clinical studies conducted under high virus loads and long-term observation periods. The results demonstrated that domestic pigs intramuscularly inoculated with 106 HAD50 of ASFV-G-∆I177L did not show the presence of any clinical sign associated with ASF when observed daily either 90 or 180 days after vaccination. In addition, necropsies conducted at the end of the experiment confirmed the absence of macroscopic internal lesions associated with the disease. These results corroborate the safety of using ASFV-G-∆I177L as a vaccine candidate.
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Borca et al. (2023) studied African swine fever (n=26). ASFV-G-∆I177L vs. Mock-inoculated with macrophage culture medium was evaluated on Presence of clinical signs associated with ASF and macroscopic internal lesions. Domestic pigs intramuscularly inoculated with a high dose of ASFV-G-∆I177L showed no clinical signs of African swine fever or macroscopic internal lesions over 90 or 180 days of observation.
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