Key result
ASFV-G-ΔI177L vaccine completely protects swine from African swine fever after virulent strain challenge.
Why the study?
African swine fever virus outbreaks caused by genotype II strains derived from the 2007 Georgia isolate have no available vaccines, necessitating development of effective vaccines derived from current outbreak strains.
Does ASFV-G-ΔI177L provide sterile immunity and protection against the virulent ASFV Georgia isolate in swine?
Does ASFV-G-ΔI177L provide sterile immunity and protection against the virulent ASFV Georgia isolate in swine?
Deletion of the I177L gene from ASFV-G produces a completely attenuated virus that safely induces sterile immunity and protects swine against the virulent ASFV Georgia isolate.
Answers are grounded in this paper and cite their sources.
Attenuates ASFV and protects swine; hypothesis-generating for vaccine development, pending field validation.
African swine fever virus (ASFV) is the etiological agent of a contagious and often lethal disease of domestic pigs that has significant economic consequences for the swine industry. The disease is devastating the swine industry in Central Europe and East Asia, with current outbreaks caused by circulating strains of ASFV derived from the 2007 Georgia isolate (ASFV-G), a genotype II ASFV. In the absence of any available vaccines, African Swine Fever (ASF) outbreak containment relies on control and culling of infected animals. Limited cross protection studies suggest that in order to ensure a vaccine is effective it must be derived from the current outbreak strain or at the very least from an isolate with the same genotype. Here we report the discovery that deletion of a previously uncharacterized gene, I177L, from the highly virulent ASFV-G produces complete virus attenuation in swine. Animals inoculated intramuscularly with the virus lacking the I177L gene, ASFV-G-ΔI177L, in a dose range of 10 2 to 10 6 HAD 50 remained clinically normal during the 28 day observational period. All ASFV-G-ΔI177L-infected animals had low viremia titers, showed no virus shedding, developed a strong virus-specific antibody response and, importantly, they were protected when challenged with the virulent parental strain ASFV-G. ASFV-G-ΔI177L is one of the few experimental vaccine candidate virus strains reported to be able to induce protection against the ASFV Georgia isolate, and the first vaccine capable of inducing sterile immunity against the current ASFV strain responsible for recent outbreaks. Importance Currently there is no commercially available vaccine against African swine fever. Outbreaks of this disease are devastating the swine industry from Central Europe to East Asia, and they are being caused by circulating strains of African swine fever virus derived from the Georgia2007 isolate. Here we report the discovery of a previously uncharacterized virus gene, which when deleted completely attenuates the Georgia isolate. Importantly, animals infected with this genetically modified virus were protected from developing ASF after challenge with the virulent parental virus. Interestingly, ASFV-G-ΔI177L confers protection even at low doses (10 2 HAD 50 ) and remains completely attenuated when inoculated at high doses (10 6 HAD 50 ), demonstrating its potential as a safe vaccine candidate. At medium doses (10 4 HAD 50 ) sterile immunity is achieved. Therefore, ASFV-G-ΔI177L is a novel efficacious experimental ASF vaccine protecting pigs from the epidemiologically relevant ASFV Georgia isolate.
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Borca et al. (2019) studied African swine fever. ASFV-G-ΔI177L was evaluated on Protection against virulent parental strain ASFV-G challenge. The ASFV-G-ΔI177L vaccine (10^2 to 10^6 HAD50) completely attenuated the virus and protected swine from developing African swine fever after challenge with the virulent parental strain.
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