Morphological changes in human neural cells following tick-borne encephalitis virus infection
1 Institute of Parasitology, Biology Centre of the Academy of Sciences of the Czech Republic and Faculty of Science, University of South Bohemia, Brani ovská 31, CZ-37005 eské Bud jovice, Czech Republic 2 Faculty of Science, Mahidol University, 6 Rama Road, Bangkok 10400, Thailand Correspondence Dan...
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creator | Ruzek, Daniel Vancova, Marie Tesarova, Martina Ahantarig, Arunee Kopecky, Jan Grubhoffer, Libor |
description | 1 Institute of Parasitology, Biology Centre of the Academy of Sciences of the Czech Republic and Faculty of Science, University of South Bohemia, Brani ovská 31, CZ-37005 eské Bud jovice, Czech Republic
2 Faculty of Science, Mahidol University, 6 Rama Road, Bangkok 10400, Thailand
Correspondence Daniel R ek ruzekd{at}paru.cas.cz
Tick-borne encephalitis (TBE) is one of the leading and most dangerous human viral neuroinfections in Europe and north-eastern Asia. The clinical manifestations include asymptomatic infections, fevers and debilitating encephalitis that might progress into chronic disease or fatal infection. To understand TBE pathology further in host nervous systems, three human neural cell lines, neuroblastoma, medulloblastoma and glioblastoma, were infected with TBE virus (TBEV). The susceptibility and virus-mediated cytopathic effect, including ultrastructural and apoptotic changes of the cells, were examined. All the neural cell lines tested were susceptible to TBEV infection. Interestingly, the neural cells produced about 100- to 10 000-fold higher virus titres than the conventional cell lines of extraneural origin, indicating the highly susceptible nature of neural cells to TBEV infection. The infection of medulloblastoma and glioblastoma cells was associated with a number of major morphological changes, including proliferation of membranes of the rough endoplasmic reticulum and extensive rearrangement of cytoskeletal structures. The TBEV-infected cells exhibited either necrotic or apoptotic morphological features. We observed ultrastructural apoptotic signs (condensation, margination and fragmentation of chromatin) and other alterations, such as vacuolation of the cytoplasm, dilatation of the endoplasmic reticulum cisternae and shrinkage of cells, accompanied by a high density of the cytoplasm. On the other hand, infected neuroblastoma cells did not exhibit proliferation of membranous structures. The virions were present in both the endoplasmic reticulum and the cytoplasm. Cells were dying preferentially by necrotic mechanisms rather than apoptosis. The neuropathological significance of these observations is discussed.
These authors contributed equally to this work. |
doi_str_mv | 10.1099/vir.0.010058-0 |
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2 Faculty of Science, Mahidol University, 6 Rama Road, Bangkok 10400, Thailand
Correspondence Daniel R ek ruzekd{at}paru.cas.cz
Tick-borne encephalitis (TBE) is one of the leading and most dangerous human viral neuroinfections in Europe and north-eastern Asia. The clinical manifestations include asymptomatic infections, fevers and debilitating encephalitis that might progress into chronic disease or fatal infection. To understand TBE pathology further in host nervous systems, three human neural cell lines, neuroblastoma, medulloblastoma and glioblastoma, were infected with TBE virus (TBEV). The susceptibility and virus-mediated cytopathic effect, including ultrastructural and apoptotic changes of the cells, were examined. All the neural cell lines tested were susceptible to TBEV infection. Interestingly, the neural cells produced about 100- to 10 000-fold higher virus titres than the conventional cell lines of extraneural origin, indicating the highly susceptible nature of neural cells to TBEV infection. The infection of medulloblastoma and glioblastoma cells was associated with a number of major morphological changes, including proliferation of membranes of the rough endoplasmic reticulum and extensive rearrangement of cytoskeletal structures. The TBEV-infected cells exhibited either necrotic or apoptotic morphological features. We observed ultrastructural apoptotic signs (condensation, margination and fragmentation of chromatin) and other alterations, such as vacuolation of the cytoplasm, dilatation of the endoplasmic reticulum cisternae and shrinkage of cells, accompanied by a high density of the cytoplasm. On the other hand, infected neuroblastoma cells did not exhibit proliferation of membranous structures. The virions were present in both the endoplasmic reticulum and the cytoplasm. Cells were dying preferentially by necrotic mechanisms rather than apoptosis. The neuropathological significance of these observations is discussed.
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2 Faculty of Science, Mahidol University, 6 Rama Road, Bangkok 10400, Thailand
Correspondence Daniel R ek ruzekd{at}paru.cas.cz
Tick-borne encephalitis (TBE) is one of the leading and most dangerous human viral neuroinfections in Europe and north-eastern Asia. The clinical manifestations include asymptomatic infections, fevers and debilitating encephalitis that might progress into chronic disease or fatal infection. To understand TBE pathology further in host nervous systems, three human neural cell lines, neuroblastoma, medulloblastoma and glioblastoma, were infected with TBE virus (TBEV). The susceptibility and virus-mediated cytopathic effect, including ultrastructural and apoptotic changes of the cells, were examined. All the neural cell lines tested were susceptible to TBEV infection. Interestingly, the neural cells produced about 100- to 10 000-fold higher virus titres than the conventional cell lines of extraneural origin, indicating the highly susceptible nature of neural cells to TBEV infection. The infection of medulloblastoma and glioblastoma cells was associated with a number of major morphological changes, including proliferation of membranes of the rough endoplasmic reticulum and extensive rearrangement of cytoskeletal structures. The TBEV-infected cells exhibited either necrotic or apoptotic morphological features. We observed ultrastructural apoptotic signs (condensation, margination and fragmentation of chromatin) and other alterations, such as vacuolation of the cytoplasm, dilatation of the endoplasmic reticulum cisternae and shrinkage of cells, accompanied by a high density of the cytoplasm. On the other hand, infected neuroblastoma cells did not exhibit proliferation of membranous structures. The virions were present in both the endoplasmic reticulum and the cytoplasm. Cells were dying preferentially by necrotic mechanisms rather than apoptosis. The neuropathological significance of these observations is discussed.
These authors contributed equally to this work.</description><subject>Apoptosis</subject><subject>Biological and medical sciences</subject><subject>Cell Death</subject><subject>Cell Line</subject><subject>Cell Membrane - ultrastructure</subject><subject>Cytoplasm - virology</subject><subject>Cytoskeleton - metabolism</subject><subject>Cytoskeleton - ultrastructure</subject><subject>Encephalitis Viruses, Tick-Borne - physiology</subject><subject>Endoplasmic Reticulum - virology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Humans</subject><subject>Microbiology</subject><subject>Miscellaneous</subject><subject>Neuroglia - ultrastructure</subject><subject>Neuroglia - virology</subject><subject>Neurons - ultrastructure</subject><subject>Neurons - virology</subject><subject>Tick-borne encephalitis virus</subject><subject>Virion - ultrastructure</subject><subject>Virology</subject><issn>0022-1317</issn><issn>1465-2099</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1v1DAQhq0K1G4LV44oF1Av2Y4_MomPqOJLKuLSK7LsdJIYEnuxk1b99yTaFRw5WRo_M_POw9gbDnsOWt88-rSHPXCAqinhjO24wqoU69cLtgMQouSS1xfsMuefAFypqj5nF1wLVCjUjv34FtNhiGPsfWvHoh1s6CkXPhTDMtlQBFrSVqdxzEUXxzE--dAXs29_lS6mQAWFlg6DHf3sc7HGWbbujtrZx_CKvezsmOn16b1i958-3t9-Ke--f_56--GubJWWc4kSmkZWDoXVzpHsHiqFToNGQOSNJamUbBSJuq6wqQmldpUW2qJy5IS8Yu-PYw8p_l4oz2byeYtsA8UlG6ylRq3-DwrgFdS4gfsj2KaYc6LOHJKfbHo2HMwm3qyXGjBH8QbWhrenyYub6OEffjK9Au9OgM2r6S7Z0Pr8lxMcUTdSrtz1kRt8Pzz5RKanMPk1h_Nx26rB1IbjKu4PgMKZ9w</recordid><startdate>20090701</startdate><enddate>20090701</enddate><creator>Ruzek, Daniel</creator><creator>Vancova, Marie</creator><creator>Tesarova, Martina</creator><creator>Ahantarig, Arunee</creator><creator>Kopecky, Jan</creator><creator>Grubhoffer, Libor</creator><general>Soc General Microbiol</general><general>Society for General Microbiology</general><scope>IQODW</scope><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>7TK</scope><scope>7U9</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>20090701</creationdate><title>Morphological changes in human neural cells following tick-borne encephalitis virus infection</title><author>Ruzek, Daniel ; Vancova, Marie ; Tesarova, Martina ; Ahantarig, Arunee ; Kopecky, Jan ; Grubhoffer, Libor</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c493t-6308835b62a9bbe3fd546b909606618ae344384e2775687e639b5929a64beb23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Apoptosis</topic><topic>Biological and medical sciences</topic><topic>Cell Death</topic><topic>Cell Line</topic><topic>Cell Membrane - ultrastructure</topic><topic>Cytoplasm - virology</topic><topic>Cytoskeleton - metabolism</topic><topic>Cytoskeleton - ultrastructure</topic><topic>Encephalitis Viruses, Tick-Borne - physiology</topic><topic>Endoplasmic Reticulum - virology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Humans</topic><topic>Microbiology</topic><topic>Miscellaneous</topic><topic>Neuroglia - ultrastructure</topic><topic>Neuroglia - virology</topic><topic>Neurons - ultrastructure</topic><topic>Neurons - virology</topic><topic>Tick-borne encephalitis virus</topic><topic>Virion - ultrastructure</topic><topic>Virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ruzek, Daniel</creatorcontrib><creatorcontrib>Vancova, Marie</creatorcontrib><creatorcontrib>Tesarova, Martina</creatorcontrib><creatorcontrib>Ahantarig, Arunee</creatorcontrib><creatorcontrib>Kopecky, Jan</creatorcontrib><creatorcontrib>Grubhoffer, Libor</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of general virology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ruzek, Daniel</au><au>Vancova, Marie</au><au>Tesarova, Martina</au><au>Ahantarig, Arunee</au><au>Kopecky, Jan</au><au>Grubhoffer, Libor</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Morphological changes in human neural cells following tick-borne encephalitis virus infection</atitle><jtitle>Journal of general virology</jtitle><addtitle>J Gen Virol</addtitle><date>2009-07-01</date><risdate>2009</risdate><volume>90</volume><issue>7</issue><spage>1649</spage><epage>1658</epage><pages>1649-1658</pages><issn>0022-1317</issn><eissn>1465-2099</eissn><coden>JGVIAY</coden><abstract>1 Institute of Parasitology, Biology Centre of the Academy of Sciences of the Czech Republic and Faculty of Science, University of South Bohemia, Brani ovská 31, CZ-37005 eské Bud jovice, Czech Republic
2 Faculty of Science, Mahidol University, 6 Rama Road, Bangkok 10400, Thailand
Correspondence Daniel R ek ruzekd{at}paru.cas.cz
Tick-borne encephalitis (TBE) is one of the leading and most dangerous human viral neuroinfections in Europe and north-eastern Asia. The clinical manifestations include asymptomatic infections, fevers and debilitating encephalitis that might progress into chronic disease or fatal infection. To understand TBE pathology further in host nervous systems, three human neural cell lines, neuroblastoma, medulloblastoma and glioblastoma, were infected with TBE virus (TBEV). The susceptibility and virus-mediated cytopathic effect, including ultrastructural and apoptotic changes of the cells, were examined. All the neural cell lines tested were susceptible to TBEV infection. Interestingly, the neural cells produced about 100- to 10 000-fold higher virus titres than the conventional cell lines of extraneural origin, indicating the highly susceptible nature of neural cells to TBEV infection. The infection of medulloblastoma and glioblastoma cells was associated with a number of major morphological changes, including proliferation of membranes of the rough endoplasmic reticulum and extensive rearrangement of cytoskeletal structures. The TBEV-infected cells exhibited either necrotic or apoptotic morphological features. We observed ultrastructural apoptotic signs (condensation, margination and fragmentation of chromatin) and other alterations, such as vacuolation of the cytoplasm, dilatation of the endoplasmic reticulum cisternae and shrinkage of cells, accompanied by a high density of the cytoplasm. On the other hand, infected neuroblastoma cells did not exhibit proliferation of membranous structures. The virions were present in both the endoplasmic reticulum and the cytoplasm. Cells were dying preferentially by necrotic mechanisms rather than apoptosis. The neuropathological significance of these observations is discussed.
These authors contributed equally to this work.</abstract><cop>Reading</cop><pub>Soc General Microbiol</pub><pmid>19264624</pmid><doi>10.1099/vir.0.010058-0</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Apoptosis Biological and medical sciences Cell Death Cell Line Cell Membrane - ultrastructure Cytoplasm - virology Cytoskeleton - metabolism Cytoskeleton - ultrastructure Encephalitis Viruses, Tick-Borne - physiology Endoplasmic Reticulum - virology Fundamental and applied biological sciences. Psychology Humans Microbiology Miscellaneous Neuroglia - ultrastructure Neuroglia - virology Neurons - ultrastructure Neurons - virology Tick-borne encephalitis virus Virion - ultrastructure Virology |
title | Morphological changes in human neural cells following tick-borne encephalitis virus infection |
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