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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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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. |
format | Online Article Text |
id | pubmed-10098061 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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