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Cellular transcripts of chicken brain tissues in response to H5N1 and Newcastle disease virus infection

BACKGROUND: Highly-pathogenic avian influenza (HPAI) H5N1 and Newcastle disease (ND) viruses are the two most important poultry viruses in the world, with the ability to cause classic central nervous system dysfunction in poultry and migratory birds. To elucidate the mechanisms of neurovirulence cau...

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Autores principales: Balasubramaniam, Vinod RMT, Wai, Tham H, Omar, Abdul R, Othman, Iekhsan, Hassan, Sharifah S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3297529/
https://www.ncbi.nlm.nih.gov/pubmed/22361110
http://dx.doi.org/10.1186/1743-422X-9-53
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author Balasubramaniam, Vinod RMT
Wai, Tham H
Omar, Abdul R
Othman, Iekhsan
Hassan, Sharifah S
author_facet Balasubramaniam, Vinod RMT
Wai, Tham H
Omar, Abdul R
Othman, Iekhsan
Hassan, Sharifah S
author_sort Balasubramaniam, Vinod RMT
collection PubMed
description BACKGROUND: Highly-pathogenic avian influenza (HPAI) H5N1 and Newcastle disease (ND) viruses are the two most important poultry viruses in the world, with the ability to cause classic central nervous system dysfunction in poultry and migratory birds. To elucidate the mechanisms of neurovirulence caused by these viruses, a preliminary study was design to analyze host's cellular responses during infections of these viruses. METHODS: An improved mRNA differential display technique (Gene Fishing™) was undertaken to analyze differentially expressed transcripts regulated during HPAI H5N1 and velogenic neurotropic NDV infections of whole brain of chickens. The identification of differentially expressed genes (DEGs) was made possible as this technique uses annealing control primers that generate reproducible, authentic and long PCR products that are detectable on agarose gels. RESULTS: Twenty-three genes were identified to be significantly regulated during infections with both viruses, where ten of the genes have been selected for validation using a TaqMan(® )based real time quantitative PCR assay. Some of the identified genes demonstrated to be key factors involving the cytoskeletal system, neural signal transduction and protein folding during stress. Interestingly, Septin 5, one of the genes isolated from HPAI H5N1-infected brain tissues has been reported to participate in the pathogenic process of Parkinson's disease. CONCLUSIONS: In this limited study, the differentially expressed genes of infected brain tissues regulated by the viruses were found not to be identical, thus suggesting that their neurovirulence and neuropathogenesis may not share similar mechanisms and pathways.
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spelling pubmed-32975292012-03-09 Cellular transcripts of chicken brain tissues in response to H5N1 and Newcastle disease virus infection Balasubramaniam, Vinod RMT Wai, Tham H Omar, Abdul R Othman, Iekhsan Hassan, Sharifah S Virol J Research BACKGROUND: Highly-pathogenic avian influenza (HPAI) H5N1 and Newcastle disease (ND) viruses are the two most important poultry viruses in the world, with the ability to cause classic central nervous system dysfunction in poultry and migratory birds. To elucidate the mechanisms of neurovirulence caused by these viruses, a preliminary study was design to analyze host's cellular responses during infections of these viruses. METHODS: An improved mRNA differential display technique (Gene Fishing™) was undertaken to analyze differentially expressed transcripts regulated during HPAI H5N1 and velogenic neurotropic NDV infections of whole brain of chickens. The identification of differentially expressed genes (DEGs) was made possible as this technique uses annealing control primers that generate reproducible, authentic and long PCR products that are detectable on agarose gels. RESULTS: Twenty-three genes were identified to be significantly regulated during infections with both viruses, where ten of the genes have been selected for validation using a TaqMan(® )based real time quantitative PCR assay. Some of the identified genes demonstrated to be key factors involving the cytoskeletal system, neural signal transduction and protein folding during stress. Interestingly, Septin 5, one of the genes isolated from HPAI H5N1-infected brain tissues has been reported to participate in the pathogenic process of Parkinson's disease. CONCLUSIONS: In this limited study, the differentially expressed genes of infected brain tissues regulated by the viruses were found not to be identical, thus suggesting that their neurovirulence and neuropathogenesis may not share similar mechanisms and pathways. BioMed Central 2012-02-23 /pmc/articles/PMC3297529/ /pubmed/22361110 http://dx.doi.org/10.1186/1743-422X-9-53 Text en Copyright ©2012 Balasubramaniam et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Balasubramaniam, Vinod RMT
Wai, Tham H
Omar, Abdul R
Othman, Iekhsan
Hassan, Sharifah S
Cellular transcripts of chicken brain tissues in response to H5N1 and Newcastle disease virus infection
title Cellular transcripts of chicken brain tissues in response to H5N1 and Newcastle disease virus infection
title_full Cellular transcripts of chicken brain tissues in response to H5N1 and Newcastle disease virus infection
title_fullStr Cellular transcripts of chicken brain tissues in response to H5N1 and Newcastle disease virus infection
title_full_unstemmed Cellular transcripts of chicken brain tissues in response to H5N1 and Newcastle disease virus infection
title_short Cellular transcripts of chicken brain tissues in response to H5N1 and Newcastle disease virus infection
title_sort cellular transcripts of chicken brain tissues in response to h5n1 and newcastle disease virus infection
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3297529/
https://www.ncbi.nlm.nih.gov/pubmed/22361110
http://dx.doi.org/10.1186/1743-422X-9-53
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