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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
Main Authors: Kaye, Stephen B, Baker, Kevin, Bonshek, Richard, Maseruka, Henry, Grinfeld, Esther, Tullo, Andrew, Easty, David L, Hart, Colin A
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container_issue 6
container_start_page 563
container_title British journal of ophthalmology
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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
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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&lt;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 &amp; purification ; Deoxyribonucleic acid ; DNA ; Gene expression ; Genomes ; Herpes viruses ; Herpesvirus 1, Human - isolation &amp; purification ; Herpesvirus 3, Human - isolation &amp; purification ; Herpesvirus 4, Human - isolation &amp; 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 &amp; 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&lt;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. 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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 &amp; 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 &amp; 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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&lt;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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