In vivo infection by a neuroinvasive neurovirulent dengue virus
Although neurological manifestations associated with dengue infections have been reported in endemic countries, the viral or host characteristics determining the infection or alteration of nervous function have not been described. In order to investigate neurobiological conditions related to central...
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description | Although neurological manifestations associated with dengue infections have been reported in endemic countries, the viral or host characteristics determining the infection or alteration of nervous function have not been described. In order to investigate neurobiological conditions related to central nervous system dengue virus (DENV) infection, we established a mouse model of neuroinfection. A DENV-4 isolate was first adapted to neuroblastoma cells, later inoculated in suckling mice brain, and finally, this D4MB-6 viral variant was inoculated intraperitoneally in Balb/c mice at different postnatal days (pnd). Virus-induced fatal encephalitis in 2 and 7 pnd mice but infected at 14 and 21 pnd mice survived. The younger mice presented encephalitis at the sixth day postinfection with limb paralysis and postural instability concomitant with efficient viral replication in brain. In this mice model, we found activated microglial cells positive to viral antigen. Neurons, oligodendrocytes, and endothelial cells were also infected by the D4MB-6 virus in neonatal mice, which showed generalized and local plasma leakage with blood–brain barrier (BBB) severe damage. These results suggest that there was a viral fitness change which led to neuroinfection only in immune or neurological immature mice. Infection of neurons, endothelial, and microglial cells may be related to detrimental function or architecture found in susceptible mice. This experimental neuroinfection model could help to have a better understanding of neurological manifestations occurring during severe cases of dengue infection. |
doi_str_mv | 10.1007/s13365-012-0117-y |
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In order to investigate neurobiological conditions related to central nervous system dengue virus (DENV) infection, we established a mouse model of neuroinfection. A DENV-4 isolate was first adapted to neuroblastoma cells, later inoculated in suckling mice brain, and finally, this D4MB-6 viral variant was inoculated intraperitoneally in Balb/c mice at different postnatal days (pnd). Virus-induced fatal encephalitis in 2 and 7 pnd mice but infected at 14 and 21 pnd mice survived. The younger mice presented encephalitis at the sixth day postinfection with limb paralysis and postural instability concomitant with efficient viral replication in brain. In this mice model, we found activated microglial cells positive to viral antigen. Neurons, oligodendrocytes, and endothelial cells were also infected by the D4MB-6 virus in neonatal mice, which showed generalized and local plasma leakage with blood–brain barrier (BBB) severe damage. These results suggest that there was a viral fitness change which led to neuroinfection only in immune or neurological immature mice. Infection of neurons, endothelial, and microglial cells may be related to detrimental function or architecture found in susceptible mice. This experimental neuroinfection model could help to have a better understanding of neurological manifestations occurring during severe cases of dengue infection.</description><identifier>ISSN: 1355-0284</identifier><identifier>EISSN: 1538-2443</identifier><identifier>DOI: 10.1007/s13365-012-0117-y</identifier><identifier>PMID: 22825914</identifier><language>eng</language><publisher>Boston: Springer US</publisher><subject>Age Factors ; Animals ; Animals, Newborn ; Biological and medical sciences ; Biomedical and Life Sciences ; Biomedicine ; Blood-Brain Barrier - immunology ; Blood-Brain Barrier - pathology ; Blood-Brain Barrier - virology ; Brain - immunology ; Brain - pathology ; Brain - virology ; Cell Line, Tumor ; Dengue - immunology ; Dengue - pathology ; Dengue - virology ; Dengue Virus - pathogenicity ; Dengue Virus - physiology ; Disease Models, Animal ; Encephalitis, Viral - immunology ; Encephalitis, Viral - pathology ; Encephalitis, Viral - virology ; Endothelial Cells - immunology ; Endothelial Cells - pathology ; Endothelial Cells - virology ; Human viral diseases ; Humans ; Immunology ; Infectious Diseases ; Medical sciences ; Mice ; Microglia - immunology ; Microglia - pathology ; Microglia - virology ; Neuroblastoma ; Neurology ; Neurons - immunology ; Neurons - pathology ; Neurons - virology ; Neurosciences ; Survival Rate ; Viral diseases ; Viral diseases of the lymphoid tissue and the blood. 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Neurovirol</addtitle><addtitle>J Neurovirol</addtitle><description>Although neurological manifestations associated with dengue infections have been reported in endemic countries, the viral or host characteristics determining the infection or alteration of nervous function have not been described. In order to investigate neurobiological conditions related to central nervous system dengue virus (DENV) infection, we established a mouse model of neuroinfection. A DENV-4 isolate was first adapted to neuroblastoma cells, later inoculated in suckling mice brain, and finally, this D4MB-6 viral variant was inoculated intraperitoneally in Balb/c mice at different postnatal days (pnd). Virus-induced fatal encephalitis in 2 and 7 pnd mice but infected at 14 and 21 pnd mice survived. The younger mice presented encephalitis at the sixth day postinfection with limb paralysis and postural instability concomitant with efficient viral replication in brain. In this mice model, we found activated microglial cells positive to viral antigen. Neurons, oligodendrocytes, and endothelial cells were also infected by the D4MB-6 virus in neonatal mice, which showed generalized and local plasma leakage with blood–brain barrier (BBB) severe damage. These results suggest that there was a viral fitness change which led to neuroinfection only in immune or neurological immature mice. Infection of neurons, endothelial, and microglial cells may be related to detrimental function or architecture found in susceptible mice. This experimental neuroinfection model could help to have a better understanding of neurological manifestations occurring during severe cases of dengue infection.</description><subject>Age Factors</subject><subject>Animals</subject><subject>Animals, Newborn</subject><subject>Biological and medical sciences</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Blood-Brain Barrier - immunology</subject><subject>Blood-Brain Barrier - pathology</subject><subject>Blood-Brain Barrier - virology</subject><subject>Brain - immunology</subject><subject>Brain - pathology</subject><subject>Brain - virology</subject><subject>Cell Line, Tumor</subject><subject>Dengue - immunology</subject><subject>Dengue - pathology</subject><subject>Dengue - virology</subject><subject>Dengue Virus - pathogenicity</subject><subject>Dengue Virus - physiology</subject><subject>Disease Models, Animal</subject><subject>Encephalitis, Viral - immunology</subject><subject>Encephalitis, Viral - pathology</subject><subject>Encephalitis, Viral - virology</subject><subject>Endothelial Cells - immunology</subject><subject>Endothelial Cells - pathology</subject><subject>Endothelial Cells - virology</subject><subject>Human viral diseases</subject><subject>Humans</subject><subject>Immunology</subject><subject>Infectious Diseases</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Microglia - immunology</subject><subject>Microglia - pathology</subject><subject>Microglia - virology</subject><subject>Neuroblastoma</subject><subject>Neurology</subject><subject>Neurons - immunology</subject><subject>Neurons - pathology</subject><subject>Neurons - virology</subject><subject>Neurosciences</subject><subject>Survival Rate</subject><subject>Viral diseases</subject><subject>Viral diseases of the lymphoid tissue and the blood. Aids</subject><subject>Viral diseases of the nervous system</subject><subject>Virology</subject><subject>Virulence</subject><issn>1355-0284</issn><issn>1538-2443</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEtLxDAQgIMo7rr6A7xIL4KXal5N25PI4mNhwYueQ5pOlizddE22hf57U7rqzUBIZuabSfgQuib4nmCcPwTCmMhSTGjcJE-HEzQnGStSyjk7jXeWxSot-AxdhLDFmDBBi3M0o7SgWUn4HD2uXNLbvk2sM6APtnVJNSQqcdD51rpeBdvDFPXWdw24Q1KD23SQjHG4RGdGNQGujucCfb48fyzf0vX762r5tE415_iQCpbxIqeaGKFNXQmha8ZMwSGraA4155UqtSjL-GEcE9SwMa1YSSBXtTJsge6muXvffnUQDnJng4amUQ7aLkgSVyEYL0lEyYRq34bgwci9tzvlB0mwHL3JyZuM3uToTQ6x5-Y4vqt2UP92_IiKwO0RUEGrxnjltA1_nOAip5xFjk5ciCW3AS-3beddVPPP69-DC4X5</recordid><startdate>20121001</startdate><enddate>20121001</enddate><creator>Velandia-Romero, Myriam Lucia</creator><creator>Acosta-Losada, Orlando</creator><creator>Castellanos, Jaime E.</creator><general>Springer US</general><general>Springer</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>7X8</scope></search><sort><creationdate>20121001</creationdate><title>In vivo infection by a neuroinvasive neurovirulent dengue virus</title><author>Velandia-Romero, Myriam Lucia ; Acosta-Losada, Orlando ; Castellanos, Jaime E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c440t-6354872c1f6cfdb66cd33f84e5b27ed44ba9c699355027e2f327eda391e7adaf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Age Factors</topic><topic>Animals</topic><topic>Animals, Newborn</topic><topic>Biological and medical sciences</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Blood-Brain Barrier - immunology</topic><topic>Blood-Brain Barrier - pathology</topic><topic>Blood-Brain Barrier - virology</topic><topic>Brain - immunology</topic><topic>Brain - pathology</topic><topic>Brain - virology</topic><topic>Cell Line, Tumor</topic><topic>Dengue - immunology</topic><topic>Dengue - pathology</topic><topic>Dengue - virology</topic><topic>Dengue Virus - pathogenicity</topic><topic>Dengue Virus - physiology</topic><topic>Disease Models, Animal</topic><topic>Encephalitis, Viral - immunology</topic><topic>Encephalitis, Viral - pathology</topic><topic>Encephalitis, Viral - virology</topic><topic>Endothelial Cells - immunology</topic><topic>Endothelial Cells - pathology</topic><topic>Endothelial Cells - virology</topic><topic>Human viral diseases</topic><topic>Humans</topic><topic>Immunology</topic><topic>Infectious Diseases</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Microglia - immunology</topic><topic>Microglia - pathology</topic><topic>Microglia - virology</topic><topic>Neuroblastoma</topic><topic>Neurology</topic><topic>Neurons - immunology</topic><topic>Neurons - pathology</topic><topic>Neurons - virology</topic><topic>Neurosciences</topic><topic>Survival Rate</topic><topic>Viral diseases</topic><topic>Viral diseases of the lymphoid tissue and the blood. Aids</topic><topic>Viral diseases of the nervous system</topic><topic>Virology</topic><topic>Virulence</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Velandia-Romero, Myriam Lucia</creatorcontrib><creatorcontrib>Acosta-Losada, Orlando</creatorcontrib><creatorcontrib>Castellanos, Jaime E.</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>MEDLINE - Academic</collection><jtitle>Journal of neurovirology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Velandia-Romero, Myriam Lucia</au><au>Acosta-Losada, Orlando</au><au>Castellanos, Jaime E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In vivo infection by a neuroinvasive neurovirulent dengue virus</atitle><jtitle>Journal of neurovirology</jtitle><stitle>J. Neurovirol</stitle><addtitle>J Neurovirol</addtitle><date>2012-10-01</date><risdate>2012</risdate><volume>18</volume><issue>5</issue><spage>374</spage><epage>387</epage><pages>374-387</pages><issn>1355-0284</issn><eissn>1538-2443</eissn><abstract>Although neurological manifestations associated with dengue infections have been reported in endemic countries, the viral or host characteristics determining the infection or alteration of nervous function have not been described. In order to investigate neurobiological conditions related to central nervous system dengue virus (DENV) infection, we established a mouse model of neuroinfection. A DENV-4 isolate was first adapted to neuroblastoma cells, later inoculated in suckling mice brain, and finally, this D4MB-6 viral variant was inoculated intraperitoneally in Balb/c mice at different postnatal days (pnd). Virus-induced fatal encephalitis in 2 and 7 pnd mice but infected at 14 and 21 pnd mice survived. The younger mice presented encephalitis at the sixth day postinfection with limb paralysis and postural instability concomitant with efficient viral replication in brain. In this mice model, we found activated microglial cells positive to viral antigen. Neurons, oligodendrocytes, and endothelial cells were also infected by the D4MB-6 virus in neonatal mice, which showed generalized and local plasma leakage with blood–brain barrier (BBB) severe damage. These results suggest that there was a viral fitness change which led to neuroinfection only in immune or neurological immature mice. Infection of neurons, endothelial, and microglial cells may be related to detrimental function or architecture found in susceptible mice. This experimental neuroinfection model could help to have a better understanding of neurological manifestations occurring during severe cases of dengue infection.</abstract><cop>Boston</cop><pub>Springer US</pub><pmid>22825914</pmid><doi>10.1007/s13365-012-0117-y</doi><tpages>14</tpages></addata></record> |
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subjects | Age Factors Animals Animals, Newborn Biological and medical sciences Biomedical and Life Sciences Biomedicine Blood-Brain Barrier - immunology Blood-Brain Barrier - pathology Blood-Brain Barrier - virology Brain - immunology Brain - pathology Brain - virology Cell Line, Tumor Dengue - immunology Dengue - pathology Dengue - virology Dengue Virus - pathogenicity Dengue Virus - physiology Disease Models, Animal Encephalitis, Viral - immunology Encephalitis, Viral - pathology Encephalitis, Viral - virology Endothelial Cells - immunology Endothelial Cells - pathology Endothelial Cells - virology Human viral diseases Humans Immunology Infectious Diseases Medical sciences Mice Microglia - immunology Microglia - pathology Microglia - virology Neuroblastoma Neurology Neurons - immunology Neurons - pathology Neurons - virology Neurosciences Survival Rate Viral diseases Viral diseases of the lymphoid tissue and the blood. Aids Viral diseases of the nervous system Virology Virulence |
title | In vivo infection by a neuroinvasive neurovirulent dengue virus |
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