Quantitative proteomics analysis revealed compromised chicken dendritic cells function at early stage of very virulent infectious Bursal disease virus infection

Chicken dendritic cells (DCs) have been demonstrated to be susceptible to infectious bursal disease virus (IBDV), a causative agent of acute and immunosuppressed disease in young chicks known as infectious bursal disease. Further functional characterization of IBDV-infected DCs of chickens is requir...

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Main Authors: Abdul Raham, Nor Yasmin, Omar, Abdul Rahman, Mohd Isa, Noor Farhanah, Hiscox, Julian, Yeap, Swee Keong
Format: Article
Language:English
Published: American Association of Avian Pathologists 2019
Online Access:http://psasir.upm.edu.my/id/eprint/81914/
http://psasir.upm.edu.my/id/eprint/81914/1/Quantitative%20proteomics%20analysis%20.pdf
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author Abdul Raham, Nor Yasmin
Omar, Abdul Rahman
Mohd Isa, Noor Farhanah
Hiscox, Julian
Yeap, Swee Keong
author_facet Abdul Raham, Nor Yasmin
Omar, Abdul Rahman
Mohd Isa, Noor Farhanah
Hiscox, Julian
Yeap, Swee Keong
author_sort Abdul Raham, Nor Yasmin
building UPM Institutional Repository
collection Online Access
description Chicken dendritic cells (DCs) have been demonstrated to be susceptible to infectious bursal disease virus (IBDV), a causative agent of acute and immunosuppressed disease in young chicks known as infectious bursal disease. Further functional characterization of IBDV-infected DCs of chickens is required to provide a better understanding on the influence of the virus on chicken bone marrow-derived dendritic cells (BM-DCs) following very virulent (vv) IBDV infection. Membrane proteins of BM-DCs were extracted and the proteins were further denatured and reduced before performing labeling with isobaric tags for relative and absolute quantitation. The differential expression protein profiles were identified and quantified using liquid chromatography coupled with tandem mass spectrometry, and later validated using flow cytometry and real-time reverse transcriptase PCR. The analysis has identified 134 differentially regulated proteins from a total of 283 proteins (cutoff values of ≤0.67, ≥1.5, and ProtScore >1.3 at 95% confidence interval), which produced high-yield membrane fractions. The entry of vvIBDV into the plasma membrane of BM-DCs was observed at 3 hr postinfection by the disruption of several important protein molecule functions, namely apoptosis, RNA/DNA/protein synthesis, and transport and cellular organization, without the activation of proteins associated with signaling. At the later stage of infection, vvIBDV induced expression of several proteins, namely CD200 receptor 1-A, integrin alpha-5, HSP-90, cathepsin, lysosomal-associated membrane protein, and Ras-related proteins, which play crucial roles in signaling, apoptosis, stress response, and antigen processing as well as in secretion of danger-associated proteins. These findings collectively indicated that the chicken DCs are expressing various receptors regarded as potential targets for pathogen interaction during viral infection. Therefore, fundamental study of the interaction of DCs and IBDV will provide valuable information in understanding the role of professional antigen-presenting cells in chickens and their molecular interactions during IBDV infection and vaccination.
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spelling upm-819142021-09-08T03:17:39Z http://psasir.upm.edu.my/id/eprint/81914/ Quantitative proteomics analysis revealed compromised chicken dendritic cells function at early stage of very virulent infectious Bursal disease virus infection Abdul Raham, Nor Yasmin Omar, Abdul Rahman Mohd Isa, Noor Farhanah Hiscox, Julian Yeap, Swee Keong Chicken dendritic cells (DCs) have been demonstrated to be susceptible to infectious bursal disease virus (IBDV), a causative agent of acute and immunosuppressed disease in young chicks known as infectious bursal disease. Further functional characterization of IBDV-infected DCs of chickens is required to provide a better understanding on the influence of the virus on chicken bone marrow-derived dendritic cells (BM-DCs) following very virulent (vv) IBDV infection. Membrane proteins of BM-DCs were extracted and the proteins were further denatured and reduced before performing labeling with isobaric tags for relative and absolute quantitation. The differential expression protein profiles were identified and quantified using liquid chromatography coupled with tandem mass spectrometry, and later validated using flow cytometry and real-time reverse transcriptase PCR. The analysis has identified 134 differentially regulated proteins from a total of 283 proteins (cutoff values of ≤0.67, ≥1.5, and ProtScore >1.3 at 95% confidence interval), which produced high-yield membrane fractions. The entry of vvIBDV into the plasma membrane of BM-DCs was observed at 3 hr postinfection by the disruption of several important protein molecule functions, namely apoptosis, RNA/DNA/protein synthesis, and transport and cellular organization, without the activation of proteins associated with signaling. At the later stage of infection, vvIBDV induced expression of several proteins, namely CD200 receptor 1-A, integrin alpha-5, HSP-90, cathepsin, lysosomal-associated membrane protein, and Ras-related proteins, which play crucial roles in signaling, apoptosis, stress response, and antigen processing as well as in secretion of danger-associated proteins. These findings collectively indicated that the chicken DCs are expressing various receptors regarded as potential targets for pathogen interaction during viral infection. Therefore, fundamental study of the interaction of DCs and IBDV will provide valuable information in understanding the role of professional antigen-presenting cells in chickens and their molecular interactions during IBDV infection and vaccination. American Association of Avian Pathologists 2019-06 Article PeerReviewed text en http://psasir.upm.edu.my/id/eprint/81914/1/Quantitative%20proteomics%20analysis%20.pdf Abdul Raham, Nor Yasmin and Omar, Abdul Rahman and Mohd Isa, Noor Farhanah and Hiscox, Julian and Yeap, Swee Keong (2019) Quantitative proteomics analysis revealed compromised chicken dendritic cells function at early stage of very virulent infectious Bursal disease virus infection. Avian Diseases, 63 (2). pp. 275-288. ISSN 0005-2086 https://bioone.org/journals/avian-diseases/volume-63/issue-2/11936-072418-Reg.1/Quantitative-Proteomics-Analysis-Revealed-Compromised-Chicken-Dendritic-Cells-Function-at/10.1637/11936-072418-Reg.1.short 10.1637/11936-072418-Reg.1.
spellingShingle Abdul Raham, Nor Yasmin
Omar, Abdul Rahman
Mohd Isa, Noor Farhanah
Hiscox, Julian
Yeap, Swee Keong
Quantitative proteomics analysis revealed compromised chicken dendritic cells function at early stage of very virulent infectious Bursal disease virus infection
title Quantitative proteomics analysis revealed compromised chicken dendritic cells function at early stage of very virulent infectious Bursal disease virus infection
title_full Quantitative proteomics analysis revealed compromised chicken dendritic cells function at early stage of very virulent infectious Bursal disease virus infection
title_fullStr Quantitative proteomics analysis revealed compromised chicken dendritic cells function at early stage of very virulent infectious Bursal disease virus infection
title_full_unstemmed Quantitative proteomics analysis revealed compromised chicken dendritic cells function at early stage of very virulent infectious Bursal disease virus infection
title_short Quantitative proteomics analysis revealed compromised chicken dendritic cells function at early stage of very virulent infectious Bursal disease virus infection
title_sort quantitative proteomics analysis revealed compromised chicken dendritic cells function at early stage of very virulent infectious bursal disease virus infection
url http://psasir.upm.edu.my/id/eprint/81914/
http://psasir.upm.edu.my/id/eprint/81914/
http://psasir.upm.edu.my/id/eprint/81914/
http://psasir.upm.edu.my/id/eprint/81914/1/Quantitative%20proteomics%20analysis%20.pdf