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Therapeutic potential of Nitazoxanide against Newcastle disease virus: A possible modulation of host cytokines

Newcastle disease (ND) is prevalent among the domesticated and the wild birds and is caused by the avian paramyxovirus serotype-I (APMV-I). It is commonly known to affect chicken, pheasant, ostrich, pigeon and waterfowl. Depending on the virulence, the velogenic NDV strains cause severe respiratory...

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Autores principales: Antony, Ferrin, Vashi, Yoya, Morla, Sudhir, Vandna, Mohan, Hari, Kumar, Sachin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7196422/
https://www.ncbi.nlm.nih.gov/pubmed/32403005
http://dx.doi.org/10.1016/j.cyto.2020.155115
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author Antony, Ferrin
Vashi, Yoya
Morla, Sudhir
Vandna
Mohan, Hari
Kumar, Sachin
author_facet Antony, Ferrin
Vashi, Yoya
Morla, Sudhir
Vandna
Mohan, Hari
Kumar, Sachin
author_sort Antony, Ferrin
collection PubMed
description Newcastle disease (ND) is prevalent among the domesticated and the wild birds and is caused by the avian paramyxovirus serotype-I (APMV-I). It is commonly known to affect chicken, pheasant, ostrich, pigeon and waterfowl. Depending on the virulence, the velogenic NDV strains cause severe respiratory and nervous disorders with a high mortality rate. The live and killed vaccines are available for the prevention of infection in the market, but the drug for the treatment is not available. Nitazoxanide (NTZ), a member of thiazolides, is an antiparasitic drug. In the present study, the effect of NTZ on the NDV replication was explored. The experiments were conducted in chicken fibroblast cells (DF-1), PBMC, embryonated chicken eggs, and two-week old chickens. The inhibition of the NDV was observed upon post-treatment of NTZ at a concentration of ~12.5 μM. Cytokine profiling of the DF-1, PBMC, and chicken embryonic tissue treated with NTZ revealed significant upregulation in all the cytokines studied except for IL-1β in DF-1 cells. It is plausible that NTZ is involved in causing immune-modulatory effects in poultry. NTZ treatment in two weeks old chicken showed significant reduction in NDV replication in trachea, and lungs, respectively, at 72 h post-infection. Encouraging results from the present study warrants repurposing NTZ as a drug for the treatment of viral infection in poultry. It will also pave the way towards understanding of similar effect against other animal pathogens.
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spelling pubmed-71964222020-05-04 Therapeutic potential of Nitazoxanide against Newcastle disease virus: A possible modulation of host cytokines Antony, Ferrin Vashi, Yoya Morla, Sudhir Vandna Mohan, Hari Kumar, Sachin Cytokine Article Newcastle disease (ND) is prevalent among the domesticated and the wild birds and is caused by the avian paramyxovirus serotype-I (APMV-I). It is commonly known to affect chicken, pheasant, ostrich, pigeon and waterfowl. Depending on the virulence, the velogenic NDV strains cause severe respiratory and nervous disorders with a high mortality rate. The live and killed vaccines are available for the prevention of infection in the market, but the drug for the treatment is not available. Nitazoxanide (NTZ), a member of thiazolides, is an antiparasitic drug. In the present study, the effect of NTZ on the NDV replication was explored. The experiments were conducted in chicken fibroblast cells (DF-1), PBMC, embryonated chicken eggs, and two-week old chickens. The inhibition of the NDV was observed upon post-treatment of NTZ at a concentration of ~12.5 μM. Cytokine profiling of the DF-1, PBMC, and chicken embryonic tissue treated with NTZ revealed significant upregulation in all the cytokines studied except for IL-1β in DF-1 cells. It is plausible that NTZ is involved in causing immune-modulatory effects in poultry. NTZ treatment in two weeks old chicken showed significant reduction in NDV replication in trachea, and lungs, respectively, at 72 h post-infection. Encouraging results from the present study warrants repurposing NTZ as a drug for the treatment of viral infection in poultry. It will also pave the way towards understanding of similar effect against other animal pathogens. Elsevier Ltd. 2020-07 2020-05-03 /pmc/articles/PMC7196422/ /pubmed/32403005 http://dx.doi.org/10.1016/j.cyto.2020.155115 Text en © 2020 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Antony, Ferrin
Vashi, Yoya
Morla, Sudhir
Vandna
Mohan, Hari
Kumar, Sachin
Therapeutic potential of Nitazoxanide against Newcastle disease virus: A possible modulation of host cytokines
title Therapeutic potential of Nitazoxanide against Newcastle disease virus: A possible modulation of host cytokines
title_full Therapeutic potential of Nitazoxanide against Newcastle disease virus: A possible modulation of host cytokines
title_fullStr Therapeutic potential of Nitazoxanide against Newcastle disease virus: A possible modulation of host cytokines
title_full_unstemmed Therapeutic potential of Nitazoxanide against Newcastle disease virus: A possible modulation of host cytokines
title_short Therapeutic potential of Nitazoxanide against Newcastle disease virus: A possible modulation of host cytokines
title_sort therapeutic potential of nitazoxanide against newcastle disease virus: a possible modulation of host cytokines
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7196422/
https://www.ncbi.nlm.nih.gov/pubmed/32403005
http://dx.doi.org/10.1016/j.cyto.2020.155115
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