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Feline herpesvirus type-1 transcription is associated with increased nasal cytokine gene transcription in cats

The etiopathogenesis of chronic nasal discharge in the cat is poorly understood. The objective of this study was to investigate alterations in transcription of genes for cytokines and chemokines in association with feline herpesvirus-1 (FHV-1) mRNA transcription. Nasal samples from 21 cats were subm...

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Published in:Veterinary microbiology 2005-07, Vol.108 (3), p.225-233
Main Authors: Johnson, Lynelle R., Maggs, David J.
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description The etiopathogenesis of chronic nasal discharge in the cat is poorly understood. The objective of this study was to investigate alterations in transcription of genes for cytokines and chemokines in association with feline herpesvirus-1 (FHV-1) mRNA transcription. Nasal samples from 21 cats were submitted for FHV-1 virus isolation (VI), traditional endpoint polymerase chain reaction (PCR) detection of FHV-1 DNA, and quantitative real-time TaqMan PCR analysis of cytokines and chemokines (interleukin [IL]-4, IL-5, IL-6, IL-10, IL-12p40, IL-16, IL-18, interferon [IFN]-γ, tumor necrosis factor [TNF]-α, and regulated on activation normal T cell expressed and secreted protein [RANTES]) and of FHV-1 mRNA and DNA. Co-infection with feline calicivirus or Chlamydophila spp. was excluded in all cats. Gene transcription in nasal samples from four specific pathogen free (SPF) cats served as the calibrator for cytokines. FHV-1 was detected by VI in 14 of 21 samples, by traditional PCR in 18 of 21 samples, and by quantitative PCR in 13 (mRNA+) and 18 (DNA+) samples. Nasal samples from cats positive for FHV-1 mRNA displayed significantly increased transcription of IL-6, IL-10, IL-12p40, IL-18, IFN-γ, TNF-α, and RANTES ( P < 0.05) in comparison to samples from cats negative for FHV-1 mRNA. The cycle threshold for FHV-1 DNA was significantly higher in cats with detectable FHV-1 mRNA ( P < 0.05). Increased transcription of cytokines/chemokines in cats with detectable mRNA for FHV-1 suggests a role for FHV-1 in nasal inflammation.
doi_str_mv 10.1016/j.vetmic.2005.04.019
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The objective of this study was to investigate alterations in transcription of genes for cytokines and chemokines in association with feline herpesvirus-1 (FHV-1) mRNA transcription. Nasal samples from 21 cats were submitted for FHV-1 virus isolation (VI), traditional endpoint polymerase chain reaction (PCR) detection of FHV-1 DNA, and quantitative real-time TaqMan PCR analysis of cytokines and chemokines (interleukin [IL]-4, IL-5, IL-6, IL-10, IL-12p40, IL-16, IL-18, interferon [IFN]-γ, tumor necrosis factor [TNF]-α, and regulated on activation normal T cell expressed and secreted protein [RANTES]) and of FHV-1 mRNA and DNA. Co-infection with feline calicivirus or Chlamydophila spp. was excluded in all cats. Gene transcription in nasal samples from four specific pathogen free (SPF) cats served as the calibrator for cytokines. FHV-1 was detected by VI in 14 of 21 samples, by traditional PCR in 18 of 21 samples, and by quantitative PCR in 13 (mRNA+) and 18 (DNA+) samples. Nasal samples from cats positive for FHV-1 mRNA displayed significantly increased transcription of IL-6, IL-10, IL-12p40, IL-18, IFN-γ, TNF-α, and RANTES ( P &lt; 0.05) in comparison to samples from cats negative for FHV-1 mRNA. The cycle threshold for FHV-1 DNA was significantly higher in cats with detectable FHV-1 mRNA ( P &lt; 0.05). 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The objective of this study was to investigate alterations in transcription of genes for cytokines and chemokines in association with feline herpesvirus-1 (FHV-1) mRNA transcription. Nasal samples from 21 cats were submitted for FHV-1 virus isolation (VI), traditional endpoint polymerase chain reaction (PCR) detection of FHV-1 DNA, and quantitative real-time TaqMan PCR analysis of cytokines and chemokines (interleukin [IL]-4, IL-5, IL-6, IL-10, IL-12p40, IL-16, IL-18, interferon [IFN]-γ, tumor necrosis factor [TNF]-α, and regulated on activation normal T cell expressed and secreted protein [RANTES]) and of FHV-1 mRNA and DNA. Co-infection with feline calicivirus or Chlamydophila spp. was excluded in all cats. Gene transcription in nasal samples from four specific pathogen free (SPF) cats served as the calibrator for cytokines. FHV-1 was detected by VI in 14 of 21 samples, by traditional PCR in 18 of 21 samples, and by quantitative PCR in 13 (mRNA+) and 18 (DNA+) samples. 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Increased transcription of cytokines/chemokines in cats with detectable mRNA for FHV-1 suggests a role for FHV-1 in nasal inflammation.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>cat diseases</subject><subject>Cat Diseases - immunology</subject><subject>Cat Diseases - virology</subject><subject>Cats</subject><subject>chronic diseases</subject><subject>cytokines</subject><subject>Cytokines - genetics</subject><subject>Cytokines - immunology</subject><subject>disease detection</subject><subject>DNA, Viral - genetics</subject><subject>Felid herpesvirus 1</subject><subject>Fundamental and applied biological sciences. 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Nasal samples from cats positive for FHV-1 mRNA displayed significantly increased transcription of IL-6, IL-10, IL-12p40, IL-18, IFN-γ, TNF-α, and RANTES ( P &lt; 0.05) in comparison to samples from cats negative for FHV-1 mRNA. The cycle threshold for FHV-1 DNA was significantly higher in cats with detectable FHV-1 mRNA ( P &lt; 0.05). Increased transcription of cytokines/chemokines in cats with detectable mRNA for FHV-1 suggests a role for FHV-1 in nasal inflammation.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>15939557</pmid><doi>10.1016/j.vetmic.2005.04.019</doi><tpages>9</tpages></addata></record>
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identifier ISSN: 0378-1135
ispartof Veterinary microbiology, 2005-07, Vol.108 (3), p.225-233
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subjects Animals
Biological and medical sciences
cat diseases
Cat Diseases - immunology
Cat Diseases - virology
Cats
chronic diseases
cytokines
Cytokines - genetics
Cytokines - immunology
disease detection
DNA, Viral - genetics
Felid herpesvirus 1
Fundamental and applied biological sciences. Psychology
gene expression regulation
Gene regulation
Herpesviridae - genetics
Herpesviridae - immunology
Herpesviridae Infections - immunology
Herpesviridae Infections - veterinary
Herpesviridae Infections - virology
Herpesvirus
inflammation
interferons
interleukins
messenger RNA
Microbiology
Miscellaneous
Mucosal immunity
Nasal Cavity - immunology
Nasal Cavity - virology
nasal mucosa
Nasal Mucosa - immunology
Nasal Mucosa - virology
polymerase chain reaction
protein secretion
respiratory tract diseases
Respiratory tract-small animal
Reverse Transcriptase Polymerase Chain Reaction - veterinary
Rhinitis - immunology
Rhinitis - veterinary
Rhinitis - virology
RNA, Messenger - biosynthesis
RNA, Messenger - genetics
Specific Pathogen-Free Organisms
Statistics, Nonparametric
T-lymphocytes
transcription (genetics)
Transcription, Genetic - immunology
tumor necrosis factors
Virology
Virus Replication - immunology
title Feline herpesvirus type-1 transcription is associated with increased nasal cytokine gene transcription in cats
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