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Updated: Jul 9, 2025

High-throughput Antiviral Assays to Screen for Inhibitors of Zika Virus Replication
Published on: October 30, 2021
Antiviral activity of nitazoxanide against Morbillivirus infections
Debora Stelitano1,2,3, Simone La Frazia4, Annalisa Ambrosino1
1Department of Experimental Medicine, University of Campania "Luigi Vanvitelli", via Santa Maria di Costantinopoli 16, 80138, Naples, Italy.
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.
Insights
Nitazoxanide (NTZ) shows promise as an antiviral treatment for measles virus (MeV) and canine distemper virus (CDV). This drug inhibits viral replication and spread by affecting the viral fusion protein, offering a potential new therapy for these concerning morbilli infections.
Area of Science:
- Virology
- Antiviral Research
- Infectious Diseases
Background:
- Measles virus (MeV) and canine distemper virus (CDV) are highly contagious morbilli viruses causing severe respiratory and neurological disease.
- Despite effective vaccines, morbilli virus infections are resurging globally, with no approved antiviral drugs available.
- Canine distemper virus (CDV) uniquely causes a high incidence of brain infections in affected animals.
Purpose of the Study:
- To investigate the potential antiviral properties of nitazoxanide (NTZ) against measles virus (MeV) and canine distemper virus (CDV).
- To explore NTZ as a therapeutic option for treating morbilli virus infections.
Main Methods:
- Live virus and cell-based assays were employed to assess the antiviral activity of nitazoxanide (NTZ).
- The study examined NTZ's effect on viral replication and the function of the viral fusion protein (F).
Main Results:
- Nitazoxanide (NTZ) demonstrated significant inhibition of both measles virus (MeV) and canine distemper virus (CDV) replication.
- NTZ acts post-entry, interfering with viral replication processes.
- The drug was found to impair viral spread by affecting the function of the viral fusion (F) protein.
Conclusions:
- Nitazoxanide (NTZ) exhibits potent antiviral activity against MeV and CDV.
- NTZ's mechanism involves inhibiting viral replication and fusion protein function, thereby limiting viral spread.
- Further exploration of NTZ as a therapeutic agent for measles and canine distemper is warranted.
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