Yuan Chen, Wang Yuchang, Zhang Xiaowen, Tian Xingyu, Liang Ying, Pan Fei, Song Haoshuai, Xia Linya, Wu Zhihui, Wang Wenqing, Zhang Xiaowen, Xie Yurui, Zhu Mingli, Hu Ruiqi, Yang Zhen, Fan Hongjie, Ma Zhe
Ministry of Agriculture Key Laboratory of Animal Bacteriology, the International Joint Laboratory of Animal Health and Food Safety, and College of Veterinary Medicine, Nanjing Agricultural University, Nanjing, Jiangsu 210095, China.
Ministry of Agriculture Key Laboratory of Animal Bacteriology, the International Joint Laboratory of Animal Health and Food Safety, and College of Veterinary Medicine, Nanjing Agricultural University, Nanjing, Jiangsu 210095, China; Jiangsu Co-innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou 225009, China.
Vet Microbiol. 2025 Mar;302:110420. doi: 10.1016/j.vetmic.2025.110420. Epub 2025 Feb 5.
Streptococcus equi subsp.zooepidemicus (SEZ) causes acute death in pigs and severely impacts the pig industry; however, comprehensive records of the clinical signs of SEZ from a bacteriological perspective are lacking. In this study, we found that piglets developed fever and a reduced appetite within 24 hours-post-infection (hpi) with SEZ and that sudden death usually started at 36 hpi. The mortality rate reached 100 % within 48 hpi. The moribund piglets presented prominent gross lesions, including swollen lungs with peripheral consolidation, enlarged and congested spleens, turbid cerebrospinal fluid (CSF), and hemorrhagic lymph nodes. Histopathologic analysis revealed widespread septicemia. The liver and spleen harbored the highest CFU burden in moribund piglets, and more SEZ proliferated in the CSF than in the brain parenchyma, suggesting an adaptation of SEZ in the CSF. By using genetically engineered chimeric McAbs with a porcine Fc region that targets the variant region of SzM (vSzM), we efficiently eliminated the SEZ burden and protected organs from gross pathological lesions in piglets. Collectively, these data provide more details concerning the systemic infection of SEZ and the potential preventive and therapeutic effects of McAbs against SEZ infection.