AI Article Synopsis

  • - Oral vaccination with the CP7_E2alf marker vaccine is being tested to better control classical swine fever (CSF) in wild boar, overcoming limitations of previous live attenuated vaccines which could not distinguish between vaccinated and infected animals.
  • - Two vaccination campaigns were conducted in hunting farms in Italy, analyzing bait uptake and immune responses, with field results showing high bait acceptance (63.7% to 98.7%) but lower antibody prevalence (33.3% to 35.1%).
  • - The study indicated that while vaccine stability was maintained under various conditions, further improvements are needed for the DIVA assay to enhance the differentiation between vaccinated and infected wild boar.

Article Abstract

Oral vaccination against classical swine fever (CSF) is a potent tool to control disease outbreaks in wild boar. So far, vaccination campaigns have been carried out using live attenuated vaccines that do not allow serological differentiation of infected from vaccinated animals (DIVA). Although this drawback is acceptable for wild boar, the use of marker vaccines would facilitate studies on disease and vaccination dynamics. Recently, the CSF marker vaccine candidate CP7_E2alf was assessed for oral immunization under laboratory conditions. Promising results prompted efforts to study the vaccine candidate under field conditions and in bait formulation. In this context, two oral vaccination campaigns were carried out with CP7_E2alf bait vaccines in two areas called 'faunistic-hunting farms' in the region of Umbria, Italy. One campaign was conducted using single vaccination, the second with the routinely employed double vaccination strategy. Both campaigns were carried out before concerted hunting actions were performed. Bait uptake, vaccine virus detection and antibody responses were assessed along with inspections upon gutting. As a comparator, seven wild boar were hand-fed with baits under laboratory conditions. In the field, bait uptake ranged from 63.7% to 98.7%, whereas antibody prevalence reached only 33.3-35.1%. The marker serology showed a strong influence of sample quality on the test outcome with a total of 85% of samples being classified correctly. Vaccine virus was not detectable. Under hand feeding conditions, six out of seven wild boar took up at least one bait, and five of them showed detectable antibody levels seven weeks after vaccination. These results were supplemented by stability tests. Appropriate stability of vaccine virus was shown both under field and laboratory conditions. In total, most results were in line with our expectations. However, optimization of the DIVA assay has to be attempted in the future.

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http://dx.doi.org/10.1016/j.vaccine.2014.02.006DOI Listing

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