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High-throughput screening unveils nitazoxanide as a potent PRRSV inhibitor by targeting NMRAL1

硝唑烷 猪繁殖与呼吸综合征病毒 病毒血症 生物 病毒学 药物发现 计算生物学 病毒 免疫学 生物信息学
作者
Zhanding Cui,Jinlong Liu,Changhao Xie,Tao Wang,Pu Sun,Jinlong Wang,Jiaoyang Li,Guo‐Xiu Li,Jicheng Qiu,Ying Zhang,Dengliang Li,Yinyan Sun,Juanbin Yin,Kun Li,Zhongwei Zhao,Hong Yuan,Xingwen Bai,Xueqing Ma,Pinghua Li,Yuanfang Fu,Huang Bao,Dong Li,Qiang Zhang,Zaixin Liu,Yimei Cao,Jing Zhang,Zengjun Lu
出处
期刊:Nature Communications [Springer Nature]
卷期号:15 (1)
标识
DOI:10.1038/s41467-024-48807-y
摘要

Abstract Porcine Reproductive and Respiratory Syndrome Virus (PRRSV) poses a major threat to the global swine industry, yet effective prevention and control measures remain elusive. This study unveils Nitazoxanide (NTZ) as a potent inhibitor of PRRSV both in vitro and in vivo. Through High-Throughput Screening techniques, 16 potential anti-PRRSV compounds are identified from a library comprising FDA-approved and pharmacopeial drugs. We show that NTZ displays strong efficacy in reducing PRRSV proliferation and transmission in a swine model, alleviating viremia and lung damage. Additionally, Tizoxanide (TIZ), the primary metabolite of NTZ, has been identified as a facilitator of NMRAL1 dimerization. This finding potentially sheds light on the underlying mechanism contributing to TIZ’s role in augmenting the sensitivity of the IFN-β pathway. These results indicate the promising potential of NTZ as a repurposed therapeutic agent for Porcine Reproductive and Respiratory Syndrome (PRRS). Additionally, they provide valuable insights into the antiviral mechanisms underlying NTZ’s effectiveness.

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