In situ hybridization for the detection of infectious laryngotracheitis virus in sections of trachea from experimentally infected chickens

An in situ hybridization procedure for the detection of infectious laryngotracheitis virus (ILTV) in experimentally infected chickens is described. Formalin-fixed, paraffin-embedded sections of trachea, taken from chickens on days 3-10 post-inoculation (p.i.) with ILTV were hybridized with a mixture...

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Veröffentlicht in:Acta veterinaria scandinavica 1998-01, Vol.39 (4), p.415-421
Hauptverfasser: Nielsen, O L, Handberg, K J, Jørgensen, P H
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Jørgensen, P H
description An in situ hybridization procedure for the detection of infectious laryngotracheitis virus (ILTV) in experimentally infected chickens is described. Formalin-fixed, paraffin-embedded sections of trachea, taken from chickens on days 3-10 post-inoculation (p.i.) with ILTV were hybridized with a mixture of 2 biotinylated, polymerase chain reaction-generated DNA fragments. The fragments correspond to sequences of the ILTV glycoprotein C and thymidine Kinase genes. In situ hybridization was seen in 7 out of 7 chickens examined on day 3 p.i., 2 out of 2 examined on day 4 p.i. and 3 out of 3 examined on day 5 p.i. No hybridization was observed in 3 out of 3 chickens examined on day 10 p.i. ILTV nucleic acid was detected in nuclei of degenerated tracheal epithelial cells and in intranuclear inclusion bodies of syncytia.
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Formalin-fixed, paraffin-embedded sections of trachea, taken from chickens on days 3-10 post-inoculation (p.i.) with ILTV were hybridized with a mixture of 2 biotinylated, polymerase chain reaction-generated DNA fragments. The fragments correspond to sequences of the ILTV glycoprotein C and thymidine Kinase genes. In situ hybridization was seen in 7 out of 7 chickens examined on day 3 p.i., 2 out of 2 examined on day 4 p.i. and 3 out of 3 examined on day 5 p.i. No hybridization was observed in 3 out of 3 chickens examined on day 10 p.i. 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Formalin-fixed, paraffin-embedded sections of trachea, taken from chickens on days 3-10 post-inoculation (p.i.) with ILTV were hybridized with a mixture of 2 biotinylated, polymerase chain reaction-generated DNA fragments. The fragments correspond to sequences of the ILTV glycoprotein C and thymidine Kinase genes. In situ hybridization was seen in 7 out of 7 chickens examined on day 3 p.i., 2 out of 2 examined on day 4 p.i. and 3 out of 3 examined on day 5 p.i. No hybridization was observed in 3 out of 3 chickens examined on day 10 p.i. ILTV nucleic acid was detected in nuclei of degenerated tracheal epithelial cells and in intranuclear inclusion bodies of syncytia.</abstract><cop>England</cop><pub>BioMed Central</pub><pmid>9926455</pmid><doi>10.1186/BF03547767</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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subjects Administration, Oral
Animals
Antibodies, Viral - blood
Chickens
DNA Primers - chemistry
DNA, Viral - analysis
DNA, Viral - chemistry
Enzyme-Linked Immunosorbent Assay - veterinary
Herpesviridae Infections - diagnosis
Herpesviridae Infections - veterinary
Herpesviridae Infections - virology
Herpesvirus 1, Gallid - genetics
Herpesvirus 1, Gallid - immunology
Herpesvirus 1, Gallid - isolation & purification
In Situ Hybridization - veterinary
Polymerase Chain Reaction - veterinary
Poultry Diseases - virology
Specific Pathogen-Free Organisms - immunology
Trachea - pathology
Trachea - virology
Tracheal Diseases - diagnosis
Tracheal Diseases - veterinary
Tracheal Diseases - virology
title In situ hybridization for the detection of infectious laryngotracheitis virus in sections of trachea from experimentally infected chickens
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