ASFV-G-∆I177L as an Effective Oral Nasal Vaccine against the Eurasia Strain of Africa Swine Fever

Manuel V. Borca(Plum Island Animal Disease Center), Elizabeth Ramírez-Medina(Plum Island Animal Disease Center), Ediane Silva(Kansas State University), Elizabeth A. Vuono(Plum Island Animal Disease Center), Ayushi Rai(Oak Ridge Associated Universities), Sarah Pruitt(Plum Island Animal Disease Center), Nallely Espinoza(Plum Island Animal Disease Center), Lauro Velázquez-Salinas(Kansas State University), Cyril G. Gay(Agricultural Research Service), Douglas P. Gladue(Plum Island Animal Disease Center)
Viruses
April 27, 2021
Cited by 107Open Access
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Abstract

The African swine fever virus (ASFV) is currently causing a pandemic affecting wild and domestic swine from Western Europe to Asia. No commercial vaccines are available to prevent African swine fever (ASF), resulting in overwhelming economic losses to the swine industry. We recently developed a recombinant vaccine candidate, ASFVG-ΔI177L, by deleting the I177L gene from the genome of the highly virulent ASFV strain Georgia (ASFV-G). ASFV-G-ΔI177L has been proven safe and highly efficacious in challenge studies using parental ASFV-G. Here, we present data demonstrating that ASFV-G-ΔI177L can be administered by the oronasal (ON) route to achieve a similar efficacy to that of intramuscular (IM) administration. Animals receiving ON ASFV-G-ΔI177L were completely protected against virulent ASFV-G challenge. As previously described, similar results were obtained when ASFV-G-ΔI177L was given intramuscularly. Interestingly, viremias induced in animals inoculated oronasally were lower than those measured in IM-inoculated animals. ASFV-specific antibody responses, mediated by IgG1, IgG2 and IgM, do not differ in animals inoculated by the ON route from that had IM inoculations. Therefore, the ASFV-G-ΔI177L vaccine candidate can be administered oronasally, a critical attribute for potential vaccination of wild swine populations.


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