Deletion of the EP402R Gene from the Genome of African Swine Fever Vaccine Strain ASFV-G-∆I177L Provides the Potential Capability of Differentiating between Infected and Vaccinated Animals

• Published in: Viruses Vol. 16; no. 3; p. 376
• Main Authors: Borca, Manuel V, Ramirez-Medina, Elizabeth, Espinoza, Nallely, Rai, Ayushi, Spinard, Edward, Velazquez-Salinas, Lauro, Valladares, Alyssa, Silva, Ediane, Burton, Leeanna, Meyers, Amanda, Clark, Jason, Wu, Ping, Gay, Cyril G, Gladue, Douglas P
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 28.02.2024; MDPI
• Subjects: Adsorption; African Swine Fever; African Swine Fever Virus; Analysis; Animals; Antibodies; Antigens; ASF vaccine; Cell culture; Complications and side effects; Diagnosis; Disease; Domestic animals; Enzyme-linked immunosorbent assay; Ep402R; EP402R marker vaccine; Erythrocytes; Gene Deletion; Genes; Genetic aspects; Genetic engineering; Genetics; Genomes; Genomics; Genotype & phenotype; Hemadsorption; Hogs; I177L; Inoculation; Macrophages; Mutants; Patient outcomes; Proteins; Recombinant Proteins - genetics; Sus scrofa; Swine; Vaccines; Vaccines, Attenuated - genetics; Vaccines, Synthetic - genetics; Viral Vaccines - genetics; Virology; Virulence; Viruses; United States; United States > US; Vietnam; Georgia; African swine fever virus; African swine fever; EP402R marker vaccine; ASF vaccine; Ep402R; I177L
• ISSN: 1999-4915; 1999-4915
• DOI: 10.3390/v16030376

The African swine fever virus (ASFV) mutant ASFV-G-∆I177L is a safe and efficacious vaccine which induces protection against the challenge of its parental virus, the Georgia 2010 isolate. Although a genetic DIVA (differentiation between infected and vaccinated animals) assay has been developed for this vaccine, still there is not a serological DIVA test for differentiating between animals vaccinated with ASFV-G-∆I177L and those infected with wild-type viruses. In this report, we describe the development of the ASFV-G-∆I177L mutant having deleted the gene, which encodes for the viral protein responsible for mediating the hemadsorption of swine erythrocytes. The resulting virus, ASFV-G-∆I177L/∆EP402R, does not have a decreased ability to replicates in swine macrophages when compared with the parental ASFV-G-∆I177L. Domestic pigs intramuscularly (IM) inoculated with either 10 or 10 HAD of ASFV-G-∆I177L/∆EP402R remained clinically normal, when compared with a group of mock-vaccinated animals, indicating the absence of residual virulence. Interestingly, an infectious virus could not be detected in the blood samples of the ASFV-G-∆I177L/∆EP402R-inoculated animals in either group at any of the time points tested. Furthermore, while all of the mock-inoculated animals presented a quick and lethal clinical form of ASF after the intramuscular inoculation challenge with 10 HAD of highly virulent parental field isolate Georgia 2010 (ASFV-G), all of the ASFV-G-∆I177L/∆EP402R-inoculated animals were protected, remaining clinically normal until the end of the observational period. Most of the ASFV-G-∆I177L/∆EP402R-inoculated pigs developed strong virus-specific antibody responses against viral antigens, reaching maximum levels at 28 days post inoculation. Importantly, all of the sera collected at that time point in the ASFV-G-∆I177L/∆EP402R-inoculated pigs did not react in a direct ELISA coated with the recombinant EP402R protein. Conversely, the EP402R protein was readily recognized by the pool of sera from the animals immunized with recombinant live attenuated vaccine candidates ASFV-G-∆I177L, ASFV-G-∆MGF, or ASFV-G-∆9GL/∆UK. Therefore, ASFV-G-∆I177L/∆EP402R is a novel, safe and efficacious candidate with potential to be used as an antigenically DIVA vaccine.