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Tomato chlorosis virus p22 interacts with NbBAG5 to inhibit autophagy and regulate virus infection

Tomato chlorosis virus (ToCV) is a member of the genus Crinivirus in the family Closteroviridae. It has a wide host range and wide distribution, causing serious harm to the vegetable industry. The autophagy pathway plays an important role in plant resistance to virus infection. Viruses and plant hos...

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Autores principales: Shang, Kaijie, Xiao, Li, Zhang, Xianping, Zang, Lianyi, Zhao, Dan, Wang, Chenchen, Wang, Xipan, Zhou, Tao, Zhu, Changxiang, Zhu, Xiaoping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10098061/
https://www.ncbi.nlm.nih.gov/pubmed/36828802
http://dx.doi.org/10.1111/mpp.13311
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author Shang, Kaijie
Xiao, Li
Zhang, Xianping
Zang, Lianyi
Zhao, Dan
Wang, Chenchen
Wang, Xipan
Zhou, Tao
Zhu, Changxiang
Zhu, Xiaoping
author_facet Shang, Kaijie
Xiao, Li
Zhang, Xianping
Zang, Lianyi
Zhao, Dan
Wang, Chenchen
Wang, Xipan
Zhou, Tao
Zhu, Changxiang
Zhu, Xiaoping
author_sort Shang, Kaijie
collection PubMed
description Tomato chlorosis virus (ToCV) is a member of the genus Crinivirus in the family Closteroviridae. It has a wide host range and wide distribution, causing serious harm to the vegetable industry. The autophagy pathway plays an important role in plant resistance to virus infection. Viruses and plant hosts coevolve in defence and antidefence processes around autophagy. In this study, the interaction between ToCV p22 and Nicotiana benthamiana B‐cell lymphoma2‐associated athanogenes5 Nicotiana benthamiana (NbBAG5) was examined. Through overexpression and down‐regulation of NbBAG5, results showed that NbBAG5 could negatively regulate ToCV infection. NbBAG5 was found to be localized in mitochondria and can change the original localization of ToCV p22, which is colocalized in mitochondria. NbBAG5 inhibited the expression of mitophagy‐related genes and the number of autophagosomes, thereby regulating viral infection by affecting mitophagy. In summary, this study demonstrated that ToCV p22 affects autophagy by interacting with NbBAG5, established the association between viral infection, BAG proteins family, and the autophagy pathway, and explained the molecular mechanism by which ToCV p22 interacts with NbBAG5 to inhibit autophagy to regulate viral infection.
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spelling pubmed-100980612023-04-14 Tomato chlorosis virus p22 interacts with NbBAG5 to inhibit autophagy and regulate virus infection Shang, Kaijie Xiao, Li Zhang, Xianping Zang, Lianyi Zhao, Dan Wang, Chenchen Wang, Xipan Zhou, Tao Zhu, Changxiang Zhu, Xiaoping Mol Plant Pathol Original Articles Tomato chlorosis virus (ToCV) is a member of the genus Crinivirus in the family Closteroviridae. It has a wide host range and wide distribution, causing serious harm to the vegetable industry. The autophagy pathway plays an important role in plant resistance to virus infection. Viruses and plant hosts coevolve in defence and antidefence processes around autophagy. In this study, the interaction between ToCV p22 and Nicotiana benthamiana B‐cell lymphoma2‐associated athanogenes5 Nicotiana benthamiana (NbBAG5) was examined. Through overexpression and down‐regulation of NbBAG5, results showed that NbBAG5 could negatively regulate ToCV infection. NbBAG5 was found to be localized in mitochondria and can change the original localization of ToCV p22, which is colocalized in mitochondria. NbBAG5 inhibited the expression of mitophagy‐related genes and the number of autophagosomes, thereby regulating viral infection by affecting mitophagy. In summary, this study demonstrated that ToCV p22 affects autophagy by interacting with NbBAG5, established the association between viral infection, BAG proteins family, and the autophagy pathway, and explained the molecular mechanism by which ToCV p22 interacts with NbBAG5 to inhibit autophagy to regulate viral infection. John Wiley and Sons Inc. 2023-02-24 /pmc/articles/PMC10098061/ /pubmed/36828802 http://dx.doi.org/10.1111/mpp.13311 Text en © 2023 The Authors. Molecular Plant Pathology published by British Society for Plant Pathology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Shang, Kaijie
Xiao, Li
Zhang, Xianping
Zang, Lianyi
Zhao, Dan
Wang, Chenchen
Wang, Xipan
Zhou, Tao
Zhu, Changxiang
Zhu, Xiaoping
Tomato chlorosis virus p22 interacts with NbBAG5 to inhibit autophagy and regulate virus infection
title Tomato chlorosis virus p22 interacts with NbBAG5 to inhibit autophagy and regulate virus infection
title_full Tomato chlorosis virus p22 interacts with NbBAG5 to inhibit autophagy and regulate virus infection
title_fullStr Tomato chlorosis virus p22 interacts with NbBAG5 to inhibit autophagy and regulate virus infection
title_full_unstemmed Tomato chlorosis virus p22 interacts with NbBAG5 to inhibit autophagy and regulate virus infection
title_short Tomato chlorosis virus p22 interacts with NbBAG5 to inhibit autophagy and regulate virus infection
title_sort tomato chlorosis virus p22 interacts with nbbag5 to inhibit autophagy and regulate virus infection
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10098061/
https://www.ncbi.nlm.nih.gov/pubmed/36828802
http://dx.doi.org/10.1111/mpp.13311
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