Standardization of an antiviral pipeline for human norovirus in human intestinal enteroids demonstrates nitazoxanide has no to weak antiviral activity

硝唑烷 诺如病毒 病毒学 抗病毒药物 生物 免疫系统 免疫学 微生物学 医学 病毒
作者
Miranda A. Lewis,Nicolás W Cortés-Penfield,Khalil Ettayebi,Ketki Patil,Gurpreet Kaur,Frederick H. Neill,Robert L. Atmar,Sasirekha Ramani,Mary K. Estes
出处
期刊:Antimicrobial Agents and Chemotherapy [American Society for Microbiology]
卷期号:67 (10) 被引量:1
标识
DOI:10.1128/aac.00636-23
摘要

Human noroviruses (HuNoVs) are the leading cause of acute gastroenteritis. In immunocompetent hosts, symptoms usually resolve within 3 days; however, in immunocompromised persons, HuNoV infection can become persistent, debilitating, and sometimes life-threatening. There are no licensed therapeutics for HuNoV due to a near half-century delay in its cultivation. Treatment for chronic HuNoV infection in immunosuppressed patients anecdotally includes nitazoxanide, a broad-spectrum antimicrobial licensed for treatment of parasite-induced gastroenteritis. Despite its off-label use for chronic HuNoV infection, nitazoxanide has not been clearly demonstrated to be an effective treatment. In this study, we standardized a pipeline for antiviral testing using multiple human small intestinal enteroid lines representing different intestinal segments and evaluated whether nitazoxanide inhibits replication of five HuNoV strains in vitro. Nitazoxanide did not exhibit high selective antiviral activity against any HuNoV strain tested, indicating it is not an effective antiviral for HuNoV infection. Human intestinal enteroids are further demonstrated as a model to serve as a preclinical platform to test antivirals against HuNoVs to treat gastrointestinal disease. Abstr.

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