基于VSV的苏丹型和本迪布焦型埃博拉病毒致死性替代小鼠模型：用于BSL-2条件下的抗体评价

Sudan (SUDV) and Bundibugyo (BDBV) ebolaviruses are major outbreak pathogens lacking approved vaccines or therapeutics. Research progress has been hampered by biosafety level 4 (BSL-4) restrictions. Here, we generated recombinant vesicular stomatitis viruses expressing SUDV or BDBV glycoproteins (VSVΔG-SUDV GP, VSVΔG-BDBV GP) and established lethal infection models in Type I interferon receptor knockout (IFNAR⁻/⁻) mice under BSL-2 conditions. Both surrogate viruses induced rapid, dose-dependent mortality with median lethal dose (LD₅₀) values below 2 PFU. Infected mice developed high viral loads in the liver, spleen, and lungs, along with leukopenia, thrombocytopenia, and elevated transaminases indicative of systemic infection and liver injury. Treatment with a single monoclonal antibody rEBOV-515 (mAb 515)) completely protected mice from lethal challenge, reducing viral loads and restoring body weight. These findings establish robust, reproducible surrogate models for SUDV and BDBV pathogenesis and therapeutic testing, filling a critical gap in filovirus research and accelerating preclinical countermeasure development.