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Differences in Neurovirulence among Isolates of Herpes Simplex Virus Types 1 and 2 in Mice using Four Routes of Infection
Differences in neurovirulence between herpes simplex virus type 1 (HSV-l) and type 2 (HSV-2) were investigated using recent clinical isolates and laboratory-passaged strains in intravaginal, intranasal, intraperitoneal, and intracerebral infections of mice. The HSV-2 isolates caused higher death rat...
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Published in: | The Journal of infectious diseases 1981-11, Vol.144 (5), p.464-471 |
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container_end_page | 471 |
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container_start_page | 464 |
container_title | The Journal of infectious diseases |
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creator | Richards, James T. Kern, Earl R. Overall, James C. Glasgow, Lowell A. |
description | Differences in neurovirulence between herpes simplex virus type 1 (HSV-l) and type 2 (HSV-2) were investigated using recent clinical isolates and laboratory-passaged strains in intravaginal, intranasal, intraperitoneal, and intracerebral infections of mice. The HSV-2 isolates caused higher death rates in all four infections. No differences in death rate were observed between recent and passaged isolates of either HSV-l or HSV-2. After intravaginal inoculation, HSV-l isolates replicated to higher titers in the vaginal mucosa, but HSV-2 isolates produced a higher death rate and a greater frequency of latent infection in lumbosacral ganglia of surviving animals. After intranasal inoculation, HSV-2 isolates again produced a higher death rate, but the frequency of latent infection in trigeminal ganglia was higher with HSV-l isolates. The data suggest that the HSV-2 isolates have an enhanced capacity to enter and replicate in the central nervous system of mice but that latency is influenced by both virus type and route of inoculation. |
doi_str_mv | 10.1093/infdis/144.5.464 |
format | article |
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The HSV-2 isolates caused higher death rates in all four infections. No differences in death rate were observed between recent and passaged isolates of either HSV-l or HSV-2. After intravaginal inoculation, HSV-l isolates replicated to higher titers in the vaginal mucosa, but HSV-2 isolates produced a higher death rate and a greater frequency of latent infection in lumbosacral ganglia of surviving animals. After intranasal inoculation, HSV-2 isolates again produced a higher death rate, but the frequency of latent infection in trigeminal ganglia was higher with HSV-l isolates. 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The HSV-2 isolates caused higher death rates in all four infections. No differences in death rate were observed between recent and passaged isolates of either HSV-l or HSV-2. After intravaginal inoculation, HSV-l isolates replicated to higher titers in the vaginal mucosa, but HSV-2 isolates produced a higher death rate and a greater frequency of latent infection in lumbosacral ganglia of surviving animals. After intranasal inoculation, HSV-2 isolates again produced a higher death rate, but the frequency of latent infection in trigeminal ganglia was higher with HSV-l isolates. The data suggest that the HSV-2 isolates have an enhanced capacity to enter and replicate in the central nervous system of mice but that latency is influenced by both virus type and route of inoculation.</description><subject>Animals</subject><subject>Central Nervous System Diseases - etiology</subject><subject>Experimental Medicine</subject><subject>Female</subject><subject>Ganglia</subject><subject>Genitalia</subject><subject>Herpes Simplex - microbiology</subject><subject>herpes simplex virus 1</subject><subject>herpes simplex virus 2</subject><subject>Human herpesvirus 1</subject><subject>Human herpesvirus 2</subject><subject>Infections</subject><subject>Inoculation</subject><subject>Mice</subject><subject>Mortality</subject><subject>Simplexvirus</subject><subject>Simplexvirus - pathogenicity</subject><subject>Virulence</subject><subject>Viruses</subject><issn>0022-1899</issn><issn>1537-6613</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1981</creationdate><recordtype>article</recordtype><recordid>eNqFUUtv1DAQthCoLKV3Lkg-ccvWzviRHGlLd1e0INGHEBfLcWzkksSLnaDuv8fRrpYjpxl9L439IfSOkiUlNZz7wbU-nVPGlnzJBHuBFpSDLISg8BItCCnLglZ1_Rq9SemJEMJAyBN0IkoJTPIF2l1552y0g7EJ-wF_sVMMf3ycuhnCug_DT7xJodNjFgSH1zZu83bn-21nn_FjliZ8v5sxivXQ4nKOufXZPCWfzddhivhbmA7-zeCsGX0Y3qJXTnfJnh3mKXq4_nR_uS5uvq42lx9vCgOEjIWsWlI10NQ1q1qqjTEN09I1pmxBgzF1BaRkICtJXCtM2zRNqV1GmDaCc4BT9GGfu43h92TTqHqfjO06PdgwJSVB8rqs6H-F-WM5r4BlIdkLTQwpRevUNvpex52iRM21qH0tKteiuMq1ZMv7Q_bU9LY9Gg49_OOf0hjikQaS45iYbyv2vE-jfT7yOv5SYn6AWn__oVb08wXcXlC1gr9x26N4</recordid><startdate>198111</startdate><enddate>198111</enddate><creator>Richards, James T.</creator><creator>Kern, Earl R.</creator><creator>Overall, James C.</creator><creator>Glasgow, Lowell A.</creator><general>The University of Chicago Press</general><general>University of Chicago Press</general><scope>BSCLL</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>7U9</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>198111</creationdate><title>Differences in Neurovirulence among Isolates of Herpes Simplex Virus Types 1 and 2 in Mice using Four Routes of Infection</title><author>Richards, James T. ; Kern, Earl R. ; Overall, James C. ; Glasgow, Lowell A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c300t-78d08b3b9948d1acccb4a7fbc2d3a3cc98302437870fd6cdbbb2af2434ac65533</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1981</creationdate><topic>Animals</topic><topic>Central Nervous System Diseases - etiology</topic><topic>Experimental Medicine</topic><topic>Female</topic><topic>Ganglia</topic><topic>Genitalia</topic><topic>Herpes Simplex - microbiology</topic><topic>herpes simplex virus 1</topic><topic>herpes simplex virus 2</topic><topic>Human herpesvirus 1</topic><topic>Human herpesvirus 2</topic><topic>Infections</topic><topic>Inoculation</topic><topic>Mice</topic><topic>Mortality</topic><topic>Simplexvirus</topic><topic>Simplexvirus - pathogenicity</topic><topic>Virulence</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Richards, James T.</creatorcontrib><creatorcontrib>Kern, Earl R.</creatorcontrib><creatorcontrib>Overall, James C.</creatorcontrib><creatorcontrib>Glasgow, Lowell A.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Richards, James T.</au><au>Kern, Earl R.</au><au>Overall, James C.</au><au>Glasgow, Lowell A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differences in Neurovirulence among Isolates of Herpes Simplex Virus Types 1 and 2 in Mice using Four Routes of Infection</atitle><jtitle>The Journal of infectious diseases</jtitle><addtitle>J Infect Dis</addtitle><date>1981-11</date><risdate>1981</risdate><volume>144</volume><issue>5</issue><spage>464</spage><epage>471</epage><pages>464-471</pages><issn>0022-1899</issn><eissn>1537-6613</eissn><abstract>Differences in neurovirulence between herpes simplex virus type 1 (HSV-l) and type 2 (HSV-2) were investigated using recent clinical isolates and laboratory-passaged strains in intravaginal, intranasal, intraperitoneal, and intracerebral infections of mice. The HSV-2 isolates caused higher death rates in all four infections. No differences in death rate were observed between recent and passaged isolates of either HSV-l or HSV-2. After intravaginal inoculation, HSV-l isolates replicated to higher titers in the vaginal mucosa, but HSV-2 isolates produced a higher death rate and a greater frequency of latent infection in lumbosacral ganglia of surviving animals. After intranasal inoculation, HSV-2 isolates again produced a higher death rate, but the frequency of latent infection in trigeminal ganglia was higher with HSV-l isolates. The data suggest that the HSV-2 isolates have an enhanced capacity to enter and replicate in the central nervous system of mice but that latency is influenced by both virus type and route of inoculation.</abstract><cop>United States</cop><pub>The University of Chicago Press</pub><pmid>6273475</pmid><doi>10.1093/infdis/144.5.464</doi><tpages>8</tpages></addata></record> |
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source | JSTOR Archival Journals and Primary Sources Collection; Oxford University Press:Jisc Collections:Oxford Journal Archive: Access period 2024-2025 |
subjects | Animals Central Nervous System Diseases - etiology Experimental Medicine Female Ganglia Genitalia Herpes Simplex - microbiology herpes simplex virus 1 herpes simplex virus 2 Human herpesvirus 1 Human herpesvirus 2 Infections Inoculation Mice Mortality Simplexvirus Simplexvirus - pathogenicity Virulence Viruses |
title | Differences in Neurovirulence among Isolates of Herpes Simplex Virus Types 1 and 2 in Mice using Four Routes of Infection |
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