Yamashita Maiko, Iwamoto Shoko, Ochiai Mariko, Sudo Kasumi, Nagasaka Takao, Saito Akito, Kozasa Takashi, Omatsu Tsutomu, Mizutani Tetsuya, Yamamoto Kinya
National Veterinary Assay Laboratory, Ministry of Agriculture, Forestry and Fisheries, 1-15-1 Tokura, Kokubunji, Tokyo 185-8511, Japan; Center for Infectious Disease Epidemiology and Prevention Research, Tokyo University of Agriculture and Technology (Cooperative Division of Veterinary Sciences), 3-5-8 Saiwai-cho, Fuchu-shi, Tokyo 183-8509, Japan.
National Veterinary Assay Laboratory, Ministry of Agriculture, Forestry and Fisheries, 1-15-1 Tokura, Kokubunji, Tokyo 185-8511, Japan.
Res Vet Sci. 2025 Jan;182:105484. doi: 10.1016/j.rvsc.2024.105484. Epub 2024 Nov 28.
Classical swine fever (CSF) re-emerged in Japan in 2018, with the epidemic virus identified as genotype 2.1, which is moderately virulent and more difficult to detect and control than the highly virulent strain. Domestic pigs were administered with GPE strain live attenuated vaccine (GPE vaccine) for outbreak management. CP7_E2alf strain recombinant live vaccine (marker vaccine), approved for differentiation of infected from vaccinated animals (DIVA), was considered optional for obtaining CSF-free country certification issued by the World Organization for Animal Health. This study aimed to assess the efficacy of both vaccines in pigs through experimental challenge tests and evaluate the DIVA ability of the marker vaccine using two enzyme-linked immunosorbent assay (ELISA) antibody detection kits. Results showed that both GPE and marker vaccines were effective against the Japanese epidemic strain; however, the ability of the ELISA antibody detection kits to discriminate the marker vaccine was limited. Therefore, to achieve CSF-free certification using vaccines with DIVA functionality, alternative detection methods and enhancement of the sensitivity and specificity of ELISA kits are needed.
2018年,日本再次出现经典猪瘟(CSF),流行病毒被鉴定为2.1基因型,该基因型具有中等毒力,比高毒株更难检测和控制。为控制疫情,给家猪接种了GPE株减毒活疫苗(GPE疫苗)。CP7_E2alf株重组活疫苗(标记疫苗)已获批准用于区分感染动物和接种动物(DIVA),被认为是获得世界动物卫生组织颁发的无CSF国家认证的可选疫苗。本研究旨在通过实验性攻毒试验评估两种疫苗对猪的效力,并使用两种酶联免疫吸附测定(ELISA)抗体检测试剂盒评估标记疫苗的DIVA能力。结果表明,GPE疫苗和标记疫苗对日本流行毒株均有效;然而,ELISA抗体检测试剂盒区分标记疫苗的能力有限。因此,为使用具有DIVA功能的疫苗获得无CSF认证,需要替代检测方法并提高ELISA试剂盒的灵敏度和特异性。