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Human herpesviruses in the cornea
AIMS To determine the sensitivity and specificity of culture, immunohistochemistry (IHC), the polymerase chain reaction (PCR), and in situ hybridisation (ISH) for detecting herpes simplex virus (HSV-1) in the cornea of patients undergoing penetrating keratoplasty. To compare the incidence of HSV-1 i...
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Published in: | British journal of ophthalmology 2000-06, Vol.84 (6), p.563-571 |
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creator | Kaye, Stephen B Baker, Kevin Bonshek, Richard Maseruka, Henry Grinfeld, Esther Tullo, Andrew Easty, David L Hart, Colin A |
description | AIMS To determine the sensitivity and specificity of culture, immunohistochemistry (IHC), the polymerase chain reaction (PCR), and in situ hybridisation (ISH) for detecting herpes simplex virus (HSV-1) in the cornea of patients undergoing penetrating keratoplasty. To compare the incidence of HSV-1 in the cornea with that of varicella zoster virus (VZV), cytomegalovirus (CMV), and Epstein-Barr virus (EBV). METHODS The corneas of 110 patients, 52 with a documented history of herpes keratitis (HSK) and 58 with non-herpetic corneal disease, were investigated using IHC, PCR, ISH, and culture. RESULTS HSV-1 DNA and antigen were detected in 82% and 74% respectively, of corneas of patients with HSK and in 22% and 15% of corneas of patients with no history of HSK. The sensitivity of PCR and IHC was 82% and 74% with a specificity of 78% and 85%, respectively. HSV-1 DNA and antigen were found more frequently and in increased amounts in corneas of patients with a short interval between their last attack of HSK and surgery. There was a good correlation between PCR and IHC in 71%. HSV-1 was isolated by culture in 2%. Latency associated transcripts were not detected using ISH. Evidence of VZV DNA or antigen was found significantly more frequently in the corneas of patients with a history of HSK (p |
doi_str_mv | 10.1136/bjo.84.6.563 |
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To compare the incidence of HSV-1 in the cornea with that of varicella zoster virus (VZV), cytomegalovirus (CMV), and Epstein-Barr virus (EBV). METHODS The corneas of 110 patients, 52 with a documented history of herpes keratitis (HSK) and 58 with non-herpetic corneal disease, were investigated using IHC, PCR, ISH, and culture. RESULTS HSV-1 DNA and antigen were detected in 82% and 74% respectively, of corneas of patients with HSK and in 22% and 15% of corneas of patients with no history of HSK. The sensitivity of PCR and IHC was 82% and 74% with a specificity of 78% and 85%, respectively. HSV-1 DNA and antigen were found more frequently and in increased amounts in corneas of patients with a short interval between their last attack of HSK and surgery. There was a good correlation between PCR and IHC in 71%. HSV-1 was isolated by culture in 2%. Latency associated transcripts were not detected using ISH. Evidence of VZV DNA or antigen was found significantly more frequently in the corneas of patients with a history of HSK (p<0.001). No evidence of EBV or CMV was found in any cornea. CONCLUSIONS PCR and IHC are both sensitive for the detection of HSV-1 in the cornea. A combination of PCR and IHC increases the specificity for the diagnosis of HSK to 97%. HSV-1 appears to be slowly removed from the cornea. VZV and HSV-1 may co-infect the cornea.</description><identifier>ISSN: 0007-1161</identifier><identifier>EISSN: 1468-2079</identifier><identifier>DOI: 10.1136/bjo.84.6.563</identifier><identifier>PMID: 10837377</identifier><identifier>CODEN: BJOPAL</identifier><language>eng</language><publisher>BMA House, Tavistock Square, London, WC1H 9JR: BMJ Publishing Group Ltd</publisher><subject>Antigens ; Carrier State - virology ; cornea ; Cornea - virology ; Cytomegalovirus ; Cytomegalovirus - isolation & purification ; Deoxyribonucleic acid ; DNA ; Gene expression ; Genomes ; Herpes viruses ; Herpesvirus 1, Human - isolation & purification ; Herpesvirus 3, Human - isolation & purification ; Herpesvirus 4, Human - isolation & purification ; HIV ; human herpesviruses ; Human immunodeficiency virus ; Humans ; Immunoenzyme Techniques ; In Situ Hybridization ; Infections ; Keratitis, Herpetic - diagnosis ; Keratitis, Herpetic - virology ; Keratoplasty, Penetrating ; Laboratories ; Original articles - Clinical science ; Patients ; Polymerase chain reaction ; Polymerase Chain Reaction - methods ; Reoperation ; Sensitivity and Specificity ; Transplants & implants</subject><ispartof>British journal of ophthalmology, 2000-06, Vol.84 (6), p.563-571</ispartof><rights>British Journal of Ophthalmology</rights><rights>Copyright: 2000 British Journal of Ophthalmology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b478t-24e1e06fecd3dc6561a9a7f6dd757814a927f5fa3d0a8ddf436915c65091c6f63</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1723495/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1723495/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10837377$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kaye, Stephen B</creatorcontrib><creatorcontrib>Baker, Kevin</creatorcontrib><creatorcontrib>Bonshek, Richard</creatorcontrib><creatorcontrib>Maseruka, Henry</creatorcontrib><creatorcontrib>Grinfeld, Esther</creatorcontrib><creatorcontrib>Tullo, Andrew</creatorcontrib><creatorcontrib>Easty, David L</creatorcontrib><creatorcontrib>Hart, Colin A</creatorcontrib><title>Human herpesviruses in the cornea</title><title>British journal of ophthalmology</title><addtitle>Br J Ophthalmol</addtitle><description>AIMS To determine the sensitivity and specificity of culture, immunohistochemistry (IHC), the polymerase chain reaction (PCR), and in situ hybridisation (ISH) for detecting herpes simplex virus (HSV-1) in the cornea of patients undergoing penetrating keratoplasty. To compare the incidence of HSV-1 in the cornea with that of varicella zoster virus (VZV), cytomegalovirus (CMV), and Epstein-Barr virus (EBV). METHODS The corneas of 110 patients, 52 with a documented history of herpes keratitis (HSK) and 58 with non-herpetic corneal disease, were investigated using IHC, PCR, ISH, and culture. RESULTS HSV-1 DNA and antigen were detected in 82% and 74% respectively, of corneas of patients with HSK and in 22% and 15% of corneas of patients with no history of HSK. The sensitivity of PCR and IHC was 82% and 74% with a specificity of 78% and 85%, respectively. HSV-1 DNA and antigen were found more frequently and in increased amounts in corneas of patients with a short interval between their last attack of HSK and surgery. There was a good correlation between PCR and IHC in 71%. HSV-1 was isolated by culture in 2%. Latency associated transcripts were not detected using ISH. Evidence of VZV DNA or antigen was found significantly more frequently in the corneas of patients with a history of HSK (p<0.001). No evidence of EBV or CMV was found in any cornea. CONCLUSIONS PCR and IHC are both sensitive for the detection of HSV-1 in the cornea. A combination of PCR and IHC increases the specificity for the diagnosis of HSK to 97%. HSV-1 appears to be slowly removed from the cornea. VZV and HSV-1 may co-infect the cornea.</description><subject>Antigens</subject><subject>Carrier State - virology</subject><subject>cornea</subject><subject>Cornea - virology</subject><subject>Cytomegalovirus</subject><subject>Cytomegalovirus - isolation & purification</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>Gene expression</subject><subject>Genomes</subject><subject>Herpes viruses</subject><subject>Herpesvirus 1, Human - isolation & purification</subject><subject>Herpesvirus 3, Human - isolation & purification</subject><subject>Herpesvirus 4, Human - isolation & purification</subject><subject>HIV</subject><subject>human herpesviruses</subject><subject>Human immunodeficiency virus</subject><subject>Humans</subject><subject>Immunoenzyme Techniques</subject><subject>In Situ Hybridization</subject><subject>Infections</subject><subject>Keratitis, Herpetic - diagnosis</subject><subject>Keratitis, Herpetic - virology</subject><subject>Keratoplasty, Penetrating</subject><subject>Laboratories</subject><subject>Original articles - Clinical science</subject><subject>Patients</subject><subject>Polymerase chain reaction</subject><subject>Polymerase Chain Reaction - methods</subject><subject>Reoperation</subject><subject>Sensitivity and Specificity</subject><subject>Transplants & implants</subject><issn>0007-1161</issn><issn>1468-2079</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><recordid>eNp90MFLwzAUBvAgis7pzbNMBL3Ymde0L8lFcEOdMPSiIl5C1qauc21n0g79782oyPTgKYT8-N7LR8gB0D4Aw_PJrOqLqI_9GNkG6UCEIggpl5ukQynlAQDCDtl1buavIQLfJjtABeOM8w45GjWFLntTYxfGLXPbOON6edmrp6aXVLY0eo9sZXruzP732SWP11cPw1Ewvr-5HV6Og0nERR2EkQFDMTNJytIEYwQtNc8wTXnMBURahjyLM81SqkWaZhFDCbGHVEKCGbIuuWhzF82kMGliytrquVrYvND2U1U6V79fynyqXqulAh6ySMY-4OQ7wFbvjXG1KnKXmPlcl6ZqnOIAMYpwNen4D5xVjS3953wWFxIRgHt11qrEVs5Zk_2sAlStmle-eSUihco37_nh-vpruK3ag6AFuavNx8-7tm8KPYjV3dNQyZfwgQ-epRp4f9r6STH7f_QX5jqZ4A</recordid><startdate>200006</startdate><enddate>200006</enddate><creator>Kaye, Stephen B</creator><creator>Baker, Kevin</creator><creator>Bonshek, Richard</creator><creator>Maseruka, Henry</creator><creator>Grinfeld, Esther</creator><creator>Tullo, Andrew</creator><creator>Easty, David L</creator><creator>Hart, Colin A</creator><general>BMJ Publishing Group Ltd</general><general>BMJ Publishing Group LTD</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>200006</creationdate><title>Human herpesviruses in the cornea</title><author>Kaye, Stephen B ; Baker, Kevin ; Bonshek, Richard ; Maseruka, Henry ; Grinfeld, Esther ; Tullo, Andrew ; Easty, David L ; Hart, Colin A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b478t-24e1e06fecd3dc6561a9a7f6dd757814a927f5fa3d0a8ddf436915c65091c6f63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Antigens</topic><topic>Carrier State - virology</topic><topic>cornea</topic><topic>Cornea - virology</topic><topic>Cytomegalovirus</topic><topic>Cytomegalovirus - isolation & purification</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>Gene expression</topic><topic>Genomes</topic><topic>Herpes viruses</topic><topic>Herpesvirus 1, Human - isolation & purification</topic><topic>Herpesvirus 3, Human - isolation & purification</topic><topic>Herpesvirus 4, Human - isolation & purification</topic><topic>HIV</topic><topic>human herpesviruses</topic><topic>Human immunodeficiency virus</topic><topic>Humans</topic><topic>Immunoenzyme Techniques</topic><topic>In Situ Hybridization</topic><topic>Infections</topic><topic>Keratitis, Herpetic - diagnosis</topic><topic>Keratitis, Herpetic - virology</topic><topic>Keratoplasty, Penetrating</topic><topic>Laboratories</topic><topic>Original articles - Clinical science</topic><topic>Patients</topic><topic>Polymerase chain reaction</topic><topic>Polymerase Chain Reaction - methods</topic><topic>Reoperation</topic><topic>Sensitivity and Specificity</topic><topic>Transplants & implants</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kaye, Stephen B</creatorcontrib><creatorcontrib>Baker, Kevin</creatorcontrib><creatorcontrib>Bonshek, Richard</creatorcontrib><creatorcontrib>Maseruka, Henry</creatorcontrib><creatorcontrib>Grinfeld, Esther</creatorcontrib><creatorcontrib>Tullo, Andrew</creatorcontrib><creatorcontrib>Easty, David L</creatorcontrib><creatorcontrib>Hart, Colin 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>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>British journal of ophthalmology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kaye, Stephen B</au><au>Baker, Kevin</au><au>Bonshek, Richard</au><au>Maseruka, Henry</au><au>Grinfeld, Esther</au><au>Tullo, Andrew</au><au>Easty, David L</au><au>Hart, Colin A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Human herpesviruses in the cornea</atitle><jtitle>British journal of ophthalmology</jtitle><addtitle>Br J Ophthalmol</addtitle><date>2000-06</date><risdate>2000</risdate><volume>84</volume><issue>6</issue><spage>563</spage><epage>571</epage><pages>563-571</pages><issn>0007-1161</issn><eissn>1468-2079</eissn><coden>BJOPAL</coden><abstract>AIMS To determine the sensitivity and specificity of culture, immunohistochemistry (IHC), the polymerase chain reaction (PCR), and in situ hybridisation (ISH) for detecting herpes simplex virus (HSV-1) in the cornea of patients undergoing penetrating keratoplasty. To compare the incidence of HSV-1 in the cornea with that of varicella zoster virus (VZV), cytomegalovirus (CMV), and Epstein-Barr virus (EBV). METHODS The corneas of 110 patients, 52 with a documented history of herpes keratitis (HSK) and 58 with non-herpetic corneal disease, were investigated using IHC, PCR, ISH, and culture. RESULTS HSV-1 DNA and antigen were detected in 82% and 74% respectively, of corneas of patients with HSK and in 22% and 15% of corneas of patients with no history of HSK. The sensitivity of PCR and IHC was 82% and 74% with a specificity of 78% and 85%, respectively. HSV-1 DNA and antigen were found more frequently and in increased amounts in corneas of patients with a short interval between their last attack of HSK and surgery. There was a good correlation between PCR and IHC in 71%. HSV-1 was isolated by culture in 2%. Latency associated transcripts were not detected using ISH. Evidence of VZV DNA or antigen was found significantly more frequently in the corneas of patients with a history of HSK (p<0.001). No evidence of EBV or CMV was found in any cornea. CONCLUSIONS PCR and IHC are both sensitive for the detection of HSV-1 in the cornea. A combination of PCR and IHC increases the specificity for the diagnosis of HSK to 97%. HSV-1 appears to be slowly removed from the cornea. VZV and HSV-1 may co-infect the cornea.</abstract><cop>BMA House, Tavistock Square, London, WC1H 9JR</cop><pub>BMJ Publishing Group Ltd</pub><pmid>10837377</pmid><doi>10.1136/bjo.84.6.563</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antigens Carrier State - virology cornea Cornea - virology Cytomegalovirus Cytomegalovirus - isolation & purification Deoxyribonucleic acid DNA Gene expression Genomes Herpes viruses Herpesvirus 1, Human - isolation & purification Herpesvirus 3, Human - isolation & purification Herpesvirus 4, Human - isolation & purification HIV human herpesviruses Human immunodeficiency virus Humans Immunoenzyme Techniques In Situ Hybridization Infections Keratitis, Herpetic - diagnosis Keratitis, Herpetic - virology Keratoplasty, Penetrating Laboratories Original articles - Clinical science Patients Polymerase chain reaction Polymerase Chain Reaction - methods Reoperation Sensitivity and Specificity Transplants & implants |
title | Human herpesviruses in the cornea |
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