Antiviral activity of nitazoxanide against Morbillivirus infections

IF 3.5 4区 医学 Q2 IMMUNOLOGY
Debora Stelitano , Simone La Frazia , Annalisa Ambrosino , Carla Zannella , Daniel Tay , Valentina Iovane , Serena Montagnaro , Anna De Filippis , Maria Gabriella Santoro , Matteo Porotto , Massimiliano Galdiero
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Abstract

The measles virus (MeV) and canine distemper virus (CDV) belong to the genus Morbillivirus of the Paramyxoviridae family. They are enveloped viruses harboring a non-segmented negative-sense RNA. Morbilliviruses are extremely contagious and transmitted through infectious aerosol droplets. Both MeV and CDV may cause respiratory infections and fatal encephalitis, although a high incidence of brain infections is unique to CDV. Despite the availability of a safe and effective vaccine against these viruses, in recent years we are witnessing a strong resurgence of Morbillivirus infection. Measles still kills more than 100,000 people each year, and CDV causes widespread outbreaks, especially among wild animals, including non-human primates.

No drugs are currently approved for MeV and CDV. Therefore, the identification of effective antiviral agents represents an unmet medical need. Here, we have investigated the potential antiviral properties of nitazoxanide (NTZ) against MeV and CDV. Antiviral activity was explored with live virus and cell-based assays. NTZ is a thiazolide that is approved by the FDA as an antiprotozoal agent for the treatment of Giardia intestinalis and Cryptosporidium parvum. Further, nitazoxanide and its metabolite tizoxanide have recently emerged as broad-spectrum antiviral agents. We found that NTZ blocks the MeV and CDV replication, acting at the post-entry level. Moreover, we showed that NTZ affects the function of the viral fusion protein (F), impairing viral spread. Our results indicate that NTZ should be further explored as a therapeutic option in measles and canine distemper virus treatment.

硝唑尼特对麻疹病毒感染的抗病毒活性
麻疹病毒(MeV)和犬瘟热病毒(CDV)同属副粘病毒科麻疹病毒属。它们是包膜病毒,含有非节段负义RNA。麻疹病毒具有极强的传染性,通过具有传染性的气溶胶飞沫传播。MeV和CDV都可能引起呼吸道感染和致命的脑炎,尽管CDV特有的脑部感染发生率很高。尽管有针对这些病毒的安全有效的疫苗,但近年来,我们目睹了麻疹病毒感染的强劲死灰复燃。麻疹每年仍导致10多万人死亡,CDV引起广泛爆发,特别是在野生动物中,包括非人灵长类动物。目前还没有批准用于MeV和CDV的药物。因此,确定有效的抗病毒药物代表着尚未满足的医疗需求。本文研究了硝唑尼特(nitazoxanide, NTZ)对麻疹病毒MeV和CDV的潜在抗病毒特性。抗病毒活性通过活病毒和基于细胞的实验来探索。NTZ是一种噻唑类药物,已被FDA批准作为治疗肠贾第虫和小隐孢子虫的抗虫剂。此外,nitazoxanide及其代谢物tizoxanide最近作为广谱抗病毒药物出现。我们发现NTZ阻断麻疹和犬瘟热病毒的复制,在进入后水平起作用。此外,我们还发现NTZ影响病毒融合蛋白(F)的功能,损害病毒的传播。我们的结果表明,NTZ在麻疹和犬瘟热病毒的治疗中值得进一步探索。
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来源期刊
Journal of Virus Eradication
Journal of Virus Eradication Medicine-Public Health, Environmental and Occupational Health
CiteScore
6.10
自引率
1.80%
发文量
28
审稿时长
39 weeks
期刊介绍: The Journal of Virus Eradication aims to provide a specialist, open-access forum to publish work in the rapidly developing field of virus eradication. The Journal covers all human viruses, in the context of new therapeutic strategies, as well as societal eradication of viral infections with preventive interventions. The Journal is aimed at the international community involved in the prevention and management of viral infections. It provides an academic forum for the publication of original research into viral reservoirs, viral persistence and virus eradication and ultimately development of cures. The Journal not only publishes original research, but provides an opportunity for opinions, reviews, case studies and comments on the published literature. It focusses on evidence-based medicine as the major thrust in the successful management of viral infections.The Journal encompasses virological, immunological, epidemiological, modelling, pharmacological, pre-clinical and in vitro, as well as clinical, data including but not limited to drugs, immunotherapy and gene therapy. It is an important source of information on the development of vaccine programs and preventative measures aimed at virus eradication.
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