Three‐dimensional reconstruction and comparison of vacuolar membranes in response to viral infection
The vacuole is a unique plant organelle that plays an important role in maintaining cellular homeostasis under various environmental stress conditions. However, the effects of biotic stress on vacuole structure has not been examined using three‐dimensional (3D) visualization. Here, we performed 3D e...
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Veröffentlicht in: | Journal of integrative plant biology 2021-02, Vol.63 (2), p.353-364 |
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creator | Wang, Xueting Ma, Juncai Jin, Xuejiao Yue, Ning Gao, Peng Mai, Keith Ka Ki Wang, Xian‐Bing Li, Dawei Kang, Byung‐Ho Zhang, Yongliang |
description | The vacuole is a unique plant organelle that plays an important role in maintaining cellular homeostasis under various environmental stress conditions. However, the effects of biotic stress on vacuole structure has not been examined using three‐dimensional (3D) visualization. Here, we performed 3D electron tomography to compare the ultrastructural changes in the vacuole during infection with different viruses. The 3D models revealed that vacuoles are remodeled in cells infected with cucumber mosaic virus (CMV) or tobacco necrosis virus A Chinese isolate (TNV‐AC), resulting in the formation of spherules at the periphery of the vacuole. These spherules contain neck‐like channels that connect their interior with the cytosol. Confocal microscopy of CMV replication proteins 1a and 2a and TNV‐AC auxiliary replication protein p23 showed that all of these proteins localize to the tonoplast. Electron microscopy revealed that the expression of these replication proteins alone is sufficient to induce spherule formation on the tonoplast, suggesting that these proteins play prominent roles in inducing vacuolar membrane remodeling. This is the first report of the 3D structures of viral replication factories built on the tonoplasts. These findings contribute to our understanding of vacuole biogenesis under normal conditions and during assembly of plant (+) RNA virus replication complexes.
Viruses build their replication factories on various intracellular organelles for multiplication. Here, the first three‐dimensional structures of viral replication factories established on the vacuole enhance our understanding of viral replication processes and may enable the development of antiviral strategies in plants. |
doi_str_mv | 10.1111/jipb.13027 |
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Viruses build their replication factories on various intracellular organelles for multiplication. Here, the first three‐dimensional structures of viral replication factories established on the vacuole enhance our understanding of viral replication processes and may enable the development of antiviral strategies in plants.</description><identifier>ISSN: 1672-9072</identifier><identifier>EISSN: 1744-7909</identifier><identifier>DOI: 10.1111/jipb.13027</identifier><identifier>PMID: 33085164</identifier><language>eng</language><publisher>China (Republic : 1949- ): Wiley Subscription Services, Inc</publisher><subject>comparison ; Confocal microscopy ; cucumber mosaic virus ; Cucumovirus - physiology ; Cucumovirus - ultrastructure ; Cytosol ; Electron Microscope Tomography ; Electron microscopy ; electron tomography ; Environmental stress ; Homeostasis ; Imaging, Three-Dimensional ; Infections ; Intracellular Membranes - metabolism ; Intracellular Membranes - ultrastructure ; Membranes ; Microscopy ; Necrosis ; Nicotiana - cytology ; Plant Diseases - virology ; Plant Epidermis - cytology ; Plant Epidermis - ultrastructure ; Plant Epidermis - virology ; Plant virus diseases ; Plant Viruses - physiology ; Plant Viruses - ultrastructure ; Proteins ; Replication ; RNA viruses ; Spherules ; Subcellular Fractions - metabolism ; Three dimensional models ; Tobacco ; tobacco necrosis virus A ; Tombusviridae - physiology ; Tombusviridae - ultrastructure ; Tonoplasts ; vacuole ; Vacuoles ; Vacuoles - metabolism ; Vacuoles - ultrastructure ; Viral infections ; Viral Proteins - metabolism ; viral replication ; Virus Replication - physiology ; Viruses</subject><ispartof>Journal of integrative plant biology, 2021-02, Vol.63 (2), p.353-364</ispartof><rights>2020 Institute of Botany, Chinese Academy of Sciences</rights><rights>2020 Institute of Botany, Chinese Academy of Sciences.</rights><rights>2021 Institute of Botany, Chinese Academy of Sciences</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4597-33b877d86b97d3629d4814ff2e36caea38ea31e23e9968c4b8503ebbd528a43c3</citedby><cites>FETCH-LOGICAL-c4597-33b877d86b97d3629d4814ff2e36caea38ea31e23e9968c4b8503ebbd528a43c3</cites><orcidid>0000-0002-6790-1044 ; 0000-0002-4299-2170</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fjipb.13027$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fjipb.13027$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1412,27905,27906,45555,45556</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33085164$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Xueting</creatorcontrib><creatorcontrib>Ma, Juncai</creatorcontrib><creatorcontrib>Jin, Xuejiao</creatorcontrib><creatorcontrib>Yue, Ning</creatorcontrib><creatorcontrib>Gao, Peng</creatorcontrib><creatorcontrib>Mai, Keith Ka Ki</creatorcontrib><creatorcontrib>Wang, Xian‐Bing</creatorcontrib><creatorcontrib>Li, Dawei</creatorcontrib><creatorcontrib>Kang, Byung‐Ho</creatorcontrib><creatorcontrib>Zhang, Yongliang</creatorcontrib><title>Three‐dimensional reconstruction and comparison of vacuolar membranes in response to viral infection</title><title>Journal of integrative plant biology</title><addtitle>J Integr Plant Biol</addtitle><description>The vacuole is a unique plant organelle that plays an important role in maintaining cellular homeostasis under various environmental stress conditions. However, the effects of biotic stress on vacuole structure has not been examined using three‐dimensional (3D) visualization. Here, we performed 3D electron tomography to compare the ultrastructural changes in the vacuole during infection with different viruses. The 3D models revealed that vacuoles are remodeled in cells infected with cucumber mosaic virus (CMV) or tobacco necrosis virus A Chinese isolate (TNV‐AC), resulting in the formation of spherules at the periphery of the vacuole. These spherules contain neck‐like channels that connect their interior with the cytosol. Confocal microscopy of CMV replication proteins 1a and 2a and TNV‐AC auxiliary replication protein p23 showed that all of these proteins localize to the tonoplast. Electron microscopy revealed that the expression of these replication proteins alone is sufficient to induce spherule formation on the tonoplast, suggesting that these proteins play prominent roles in inducing vacuolar membrane remodeling. This is the first report of the 3D structures of viral replication factories built on the tonoplasts. These findings contribute to our understanding of vacuole biogenesis under normal conditions and during assembly of plant (+) RNA virus replication complexes.
Viruses build their replication factories on various intracellular organelles for multiplication. Here, the first three‐dimensional structures of viral replication factories established on the vacuole enhance our understanding of viral replication processes and may enable the development of antiviral strategies in plants.</description><subject>comparison</subject><subject>Confocal microscopy</subject><subject>cucumber mosaic virus</subject><subject>Cucumovirus - physiology</subject><subject>Cucumovirus - ultrastructure</subject><subject>Cytosol</subject><subject>Electron Microscope Tomography</subject><subject>Electron microscopy</subject><subject>electron tomography</subject><subject>Environmental stress</subject><subject>Homeostasis</subject><subject>Imaging, Three-Dimensional</subject><subject>Infections</subject><subject>Intracellular Membranes - metabolism</subject><subject>Intracellular Membranes - ultrastructure</subject><subject>Membranes</subject><subject>Microscopy</subject><subject>Necrosis</subject><subject>Nicotiana - cytology</subject><subject>Plant Diseases - virology</subject><subject>Plant Epidermis - cytology</subject><subject>Plant Epidermis - ultrastructure</subject><subject>Plant Epidermis - virology</subject><subject>Plant virus diseases</subject><subject>Plant Viruses - physiology</subject><subject>Plant Viruses - ultrastructure</subject><subject>Proteins</subject><subject>Replication</subject><subject>RNA viruses</subject><subject>Spherules</subject><subject>Subcellular Fractions - metabolism</subject><subject>Three dimensional models</subject><subject>Tobacco</subject><subject>tobacco necrosis virus A</subject><subject>Tombusviridae - physiology</subject><subject>Tombusviridae - ultrastructure</subject><subject>Tonoplasts</subject><subject>vacuole</subject><subject>Vacuoles</subject><subject>Vacuoles - metabolism</subject><subject>Vacuoles - ultrastructure</subject><subject>Viral infections</subject><subject>Viral Proteins - metabolism</subject><subject>viral replication</subject><subject>Virus Replication - physiology</subject><subject>Viruses</subject><issn>1672-9072</issn><issn>1744-7909</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMtKxDAUhoMo3jc-gBTciFDNrbksVbwi6GJclzQ9xQxtU5Op4s5H8Bl9EjPO6MKFgUNywnc-kh-hPYKPSVonUzdUx4RhKlfQJpGc51JjvZrOQtJcY0k30FaMU4yZwoKuow3GsCqI4JuomTwFgM_3j9p10Efne9NmAazv4yyMdpYuMtPXmfXdYIKLqfVN9mLs6FsTsg66KpgeYub6NBaHNAfZzGcvLiSR6xv4duygtca0EXaX-zZ6vLyYnF_nd_dXN-end7nlhZY5Y5WSslai0rJmguqaK8KbhgIT1oBhKhUBykBroSyvVIEZVFVdUGU4s2wbHS68Q_DPI8RZ2blooW3TG_0YS8oLqqUQkif04A869WNI359TSkmspCgSdbSgbPAxBmjKIbjOhLeS4HKefjlPv_xOP8H7S-VYdVD_oj9xJ4AsgFfXwts_qvL25uFsIf0CbOmRhg</recordid><startdate>202102</startdate><enddate>202102</enddate><creator>Wang, Xueting</creator><creator>Ma, Juncai</creator><creator>Jin, Xuejiao</creator><creator>Yue, Ning</creator><creator>Gao, Peng</creator><creator>Mai, Keith Ka Ki</creator><creator>Wang, Xian‐Bing</creator><creator>Li, Dawei</creator><creator>Kang, Byung‐Ho</creator><creator>Zhang, Yongliang</creator><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-6790-1044</orcidid><orcidid>https://orcid.org/0000-0002-4299-2170</orcidid></search><sort><creationdate>202102</creationdate><title>Three‐dimensional reconstruction and comparison of vacuolar membranes in response to viral infection</title><author>Wang, Xueting ; Ma, Juncai ; Jin, Xuejiao ; Yue, Ning ; Gao, Peng ; Mai, Keith Ka Ki ; Wang, Xian‐Bing ; Li, Dawei ; Kang, Byung‐Ho ; Zhang, Yongliang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4597-33b877d86b97d3629d4814ff2e36caea38ea31e23e9968c4b8503ebbd528a43c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>comparison</topic><topic>Confocal microscopy</topic><topic>cucumber mosaic virus</topic><topic>Cucumovirus - physiology</topic><topic>Cucumovirus - ultrastructure</topic><topic>Cytosol</topic><topic>Electron Microscope Tomography</topic><topic>Electron microscopy</topic><topic>electron tomography</topic><topic>Environmental stress</topic><topic>Homeostasis</topic><topic>Imaging, Three-Dimensional</topic><topic>Infections</topic><topic>Intracellular Membranes - metabolism</topic><topic>Intracellular Membranes - ultrastructure</topic><topic>Membranes</topic><topic>Microscopy</topic><topic>Necrosis</topic><topic>Nicotiana - cytology</topic><topic>Plant Diseases - virology</topic><topic>Plant Epidermis - cytology</topic><topic>Plant Epidermis - ultrastructure</topic><topic>Plant Epidermis - virology</topic><topic>Plant virus diseases</topic><topic>Plant Viruses - physiology</topic><topic>Plant Viruses - ultrastructure</topic><topic>Proteins</topic><topic>Replication</topic><topic>RNA viruses</topic><topic>Spherules</topic><topic>Subcellular Fractions - metabolism</topic><topic>Three dimensional models</topic><topic>Tobacco</topic><topic>tobacco necrosis virus A</topic><topic>Tombusviridae - physiology</topic><topic>Tombusviridae - ultrastructure</topic><topic>Tonoplasts</topic><topic>vacuole</topic><topic>Vacuoles</topic><topic>Vacuoles - metabolism</topic><topic>Vacuoles - ultrastructure</topic><topic>Viral infections</topic><topic>Viral Proteins - metabolism</topic><topic>viral replication</topic><topic>Virus Replication - physiology</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Xueting</creatorcontrib><creatorcontrib>Ma, Juncai</creatorcontrib><creatorcontrib>Jin, Xuejiao</creatorcontrib><creatorcontrib>Yue, Ning</creatorcontrib><creatorcontrib>Gao, Peng</creatorcontrib><creatorcontrib>Mai, Keith Ka Ki</creatorcontrib><creatorcontrib>Wang, Xian‐Bing</creatorcontrib><creatorcontrib>Li, Dawei</creatorcontrib><creatorcontrib>Kang, Byung‐Ho</creatorcontrib><creatorcontrib>Zhang, Yongliang</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of integrative plant biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Xueting</au><au>Ma, Juncai</au><au>Jin, Xuejiao</au><au>Yue, Ning</au><au>Gao, Peng</au><au>Mai, Keith Ka Ki</au><au>Wang, Xian‐Bing</au><au>Li, Dawei</au><au>Kang, Byung‐Ho</au><au>Zhang, Yongliang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Three‐dimensional reconstruction and comparison of vacuolar membranes in response to viral infection</atitle><jtitle>Journal of integrative plant biology</jtitle><addtitle>J Integr Plant Biol</addtitle><date>2021-02</date><risdate>2021</risdate><volume>63</volume><issue>2</issue><spage>353</spage><epage>364</epage><pages>353-364</pages><issn>1672-9072</issn><eissn>1744-7909</eissn><abstract>The vacuole is a unique plant organelle that plays an important role in maintaining cellular homeostasis under various environmental stress conditions. However, the effects of biotic stress on vacuole structure has not been examined using three‐dimensional (3D) visualization. Here, we performed 3D electron tomography to compare the ultrastructural changes in the vacuole during infection with different viruses. The 3D models revealed that vacuoles are remodeled in cells infected with cucumber mosaic virus (CMV) or tobacco necrosis virus A Chinese isolate (TNV‐AC), resulting in the formation of spherules at the periphery of the vacuole. These spherules contain neck‐like channels that connect their interior with the cytosol. Confocal microscopy of CMV replication proteins 1a and 2a and TNV‐AC auxiliary replication protein p23 showed that all of these proteins localize to the tonoplast. Electron microscopy revealed that the expression of these replication proteins alone is sufficient to induce spherule formation on the tonoplast, suggesting that these proteins play prominent roles in inducing vacuolar membrane remodeling. This is the first report of the 3D structures of viral replication factories built on the tonoplasts. These findings contribute to our understanding of vacuole biogenesis under normal conditions and during assembly of plant (+) RNA virus replication complexes.
Viruses build their replication factories on various intracellular organelles for multiplication. Here, the first three‐dimensional structures of viral replication factories established on the vacuole enhance our understanding of viral replication processes and may enable the development of antiviral strategies in plants.</abstract><cop>China (Republic : 1949- )</cop><pub>Wiley Subscription Services, Inc</pub><pmid>33085164</pmid><doi>10.1111/jipb.13027</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-6790-1044</orcidid><orcidid>https://orcid.org/0000-0002-4299-2170</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | comparison Confocal microscopy cucumber mosaic virus Cucumovirus - physiology Cucumovirus - ultrastructure Cytosol Electron Microscope Tomography Electron microscopy electron tomography Environmental stress Homeostasis Imaging, Three-Dimensional Infections Intracellular Membranes - metabolism Intracellular Membranes - ultrastructure Membranes Microscopy Necrosis Nicotiana - cytology Plant Diseases - virology Plant Epidermis - cytology Plant Epidermis - ultrastructure Plant Epidermis - virology Plant virus diseases Plant Viruses - physiology Plant Viruses - ultrastructure Proteins Replication RNA viruses Spherules Subcellular Fractions - metabolism Three dimensional models Tobacco tobacco necrosis virus A Tombusviridae - physiology Tombusviridae - ultrastructure Tonoplasts vacuole Vacuoles Vacuoles - metabolism Vacuoles - ultrastructure Viral infections Viral Proteins - metabolism viral replication Virus Replication - physiology Viruses |
title | Three‐dimensional reconstruction and comparison of vacuolar membranes in response to viral infection |
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