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Establishment of sheep nasal mucosa explant model and its application in antiviral research

The nasal mucosa is the first barrier to pathogen invasion through the respiratory tract. Few studies have focused on nasal resistance to invasion by respiratory pathogens due to the lack of models related to the nasal mucosa. Hence, it is necessary to construct a nasal mucosal model to study host-p...

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Autores principales: Zheng, Jian, Lin, Jian, Ma, Yichao, Yang, Chengjie, Zhong, Qiu, Li, Yuchen, Yang, Qian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10226428/
https://www.ncbi.nlm.nih.gov/pubmed/37256060
http://dx.doi.org/10.3389/fmicb.2023.1124936
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author Zheng, Jian
Lin, Jian
Ma, Yichao
Yang, Chengjie
Zhong, Qiu
Li, Yuchen
Yang, Qian
author_facet Zheng, Jian
Lin, Jian
Ma, Yichao
Yang, Chengjie
Zhong, Qiu
Li, Yuchen
Yang, Qian
author_sort Zheng, Jian
collection PubMed
description The nasal mucosa is the first barrier to pathogen invasion through the respiratory tract. Few studies have focused on nasal resistance to invasion by respiratory pathogens due to the lack of models related to the nasal mucosa. Hence, it is necessary to construct a nasal mucosal model to study host-pathogen interactions. We established a long-term in vitro sheep nasal mucosa explant model (NMEM), which exhibited typical epithelial cilia and epithelial proliferation ability within 11 days. Moreover, to evaluate whether the NMEM was suited for in vitro pathogenic study, we used pseudorabies virus (PRV) and showed that it successfully infected and produced severe lesions in the NMEM, particularly interferon (IFN)-stimulated gene product 15 (ISG15). IFN decreased significantly after the PRV infection. Similarly, we used this NMEM model to screen several antiviral substances, such as probiotics and drugs. A previous study showed that nasal commensal bacteria, particularly Bacillus subtilis, had high antiviral activity. Then, we used the NMEM to evaluate six sheep-derived B. subtilis strains and demonstrated that it significantly induced the production of IFN and expression of ISG15. The sheep-derived B. subtilis was pretreated with the sheep NMEM before the PRV infection to evaluate the antiviral effect. The results showed that NSV2 significantly inhibited infection by PRV and reduced the viral load (p < 0.05). Furthermore, NSV2 may inhibit PRV replication by enhancing ISGylation of cells. In conclusion, we established a reliable in vitro culture model of sheep NMEM, and applied it in antiviral research.
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spelling pubmed-102264282023-05-30 Establishment of sheep nasal mucosa explant model and its application in antiviral research Zheng, Jian Lin, Jian Ma, Yichao Yang, Chengjie Zhong, Qiu Li, Yuchen Yang, Qian Front Microbiol Microbiology The nasal mucosa is the first barrier to pathogen invasion through the respiratory tract. Few studies have focused on nasal resistance to invasion by respiratory pathogens due to the lack of models related to the nasal mucosa. Hence, it is necessary to construct a nasal mucosal model to study host-pathogen interactions. We established a long-term in vitro sheep nasal mucosa explant model (NMEM), which exhibited typical epithelial cilia and epithelial proliferation ability within 11 days. Moreover, to evaluate whether the NMEM was suited for in vitro pathogenic study, we used pseudorabies virus (PRV) and showed that it successfully infected and produced severe lesions in the NMEM, particularly interferon (IFN)-stimulated gene product 15 (ISG15). IFN decreased significantly after the PRV infection. Similarly, we used this NMEM model to screen several antiviral substances, such as probiotics and drugs. A previous study showed that nasal commensal bacteria, particularly Bacillus subtilis, had high antiviral activity. Then, we used the NMEM to evaluate six sheep-derived B. subtilis strains and demonstrated that it significantly induced the production of IFN and expression of ISG15. The sheep-derived B. subtilis was pretreated with the sheep NMEM before the PRV infection to evaluate the antiviral effect. The results showed that NSV2 significantly inhibited infection by PRV and reduced the viral load (p < 0.05). Furthermore, NSV2 may inhibit PRV replication by enhancing ISGylation of cells. In conclusion, we established a reliable in vitro culture model of sheep NMEM, and applied it in antiviral research. Frontiers Media S.A. 2023-05-15 /pmc/articles/PMC10226428/ /pubmed/37256060 http://dx.doi.org/10.3389/fmicb.2023.1124936 Text en Copyright © 2023 Zheng, Lin, Ma, Yang, Zhong, Li and Yang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Zheng, Jian
Lin, Jian
Ma, Yichao
Yang, Chengjie
Zhong, Qiu
Li, Yuchen
Yang, Qian
Establishment of sheep nasal mucosa explant model and its application in antiviral research
title Establishment of sheep nasal mucosa explant model and its application in antiviral research
title_full Establishment of sheep nasal mucosa explant model and its application in antiviral research
title_fullStr Establishment of sheep nasal mucosa explant model and its application in antiviral research
title_full_unstemmed Establishment of sheep nasal mucosa explant model and its application in antiviral research
title_short Establishment of sheep nasal mucosa explant model and its application in antiviral research
title_sort establishment of sheep nasal mucosa explant model and its application in antiviral research
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10226428/
https://www.ncbi.nlm.nih.gov/pubmed/37256060
http://dx.doi.org/10.3389/fmicb.2023.1124936
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