Cargando…

Time-resolved proteomics of adenovirus infected cells

Viral infections cause large problems in the world and deeper understanding of the disease mechanisms is needed. Here we present an analytical strategy to investigate the host cell protein changes during human adenovirus type 2 (HAdV-C2 or Ad2) infection of lung fibroblasts by stable isotope labelli...

Descripción completa

Detalles Bibliográficos
Autores principales: Valdés, Alberto, Zhao, Hongxing, Pettersson, Ulf, Lind, Sara Bergström
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6155545/
https://www.ncbi.nlm.nih.gov/pubmed/30252905
http://dx.doi.org/10.1371/journal.pone.0204522
_version_ 1783357920250953728
author Valdés, Alberto
Zhao, Hongxing
Pettersson, Ulf
Lind, Sara Bergström
author_facet Valdés, Alberto
Zhao, Hongxing
Pettersson, Ulf
Lind, Sara Bergström
author_sort Valdés, Alberto
collection PubMed
description Viral infections cause large problems in the world and deeper understanding of the disease mechanisms is needed. Here we present an analytical strategy to investigate the host cell protein changes during human adenovirus type 2 (HAdV-C2 or Ad2) infection of lung fibroblasts by stable isotope labelling of amino acids in cell culture (SILAC) and nanoLC-MS/MS. This work focuses on early phase of infection (6 and 12 h post-infection (hpi)) but the data is combined with previously published late phase (24 and 36 hpi) proteomics data to produce a time series covering the complete infection. As many as 2169 proteins were quantitatively monitored from 6 to 36 hpi, while some proteins were time-specific. After applying different filter criteria, 2027 and 2150 proteins were quantified at 6 and 12 hpi and among them, 431 and 544 were significantly altered at the two time points. Pathway analysis showed that the De novo purine and pyrimidine biosynthesis, Glycolysis and Cytoskeletal regulation by Rho GTPase pathways were activated early during infection while inactivation of the Integrin signalling pathway started between 6 and 12 hpi. Moreover, upstream regulator analysis predicted MYC to be activated with time of infection and protein and RNA data for genes controlled by this transcription factor showed good correlation, which validated the use of protein data for this prediction. Among the identified phosphorylation sites, a group related to glycolysis and cytoskeletal reorganization were up-regulated during infection. The results show specific aspects on how the host cell proteins, the final products in the genetic information flow, are influenced by Ad2 infection, which would be overlooked if only knowledge derived from mRNA data is considered.
format Online
Article
Text
id pubmed-6155545
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-61555452018-10-19 Time-resolved proteomics of adenovirus infected cells Valdés, Alberto Zhao, Hongxing Pettersson, Ulf Lind, Sara Bergström PLoS One Research Article Viral infections cause large problems in the world and deeper understanding of the disease mechanisms is needed. Here we present an analytical strategy to investigate the host cell protein changes during human adenovirus type 2 (HAdV-C2 or Ad2) infection of lung fibroblasts by stable isotope labelling of amino acids in cell culture (SILAC) and nanoLC-MS/MS. This work focuses on early phase of infection (6 and 12 h post-infection (hpi)) but the data is combined with previously published late phase (24 and 36 hpi) proteomics data to produce a time series covering the complete infection. As many as 2169 proteins were quantitatively monitored from 6 to 36 hpi, while some proteins were time-specific. After applying different filter criteria, 2027 and 2150 proteins were quantified at 6 and 12 hpi and among them, 431 and 544 were significantly altered at the two time points. Pathway analysis showed that the De novo purine and pyrimidine biosynthesis, Glycolysis and Cytoskeletal regulation by Rho GTPase pathways were activated early during infection while inactivation of the Integrin signalling pathway started between 6 and 12 hpi. Moreover, upstream regulator analysis predicted MYC to be activated with time of infection and protein and RNA data for genes controlled by this transcription factor showed good correlation, which validated the use of protein data for this prediction. Among the identified phosphorylation sites, a group related to glycolysis and cytoskeletal reorganization were up-regulated during infection. The results show specific aspects on how the host cell proteins, the final products in the genetic information flow, are influenced by Ad2 infection, which would be overlooked if only knowledge derived from mRNA data is considered. Public Library of Science 2018-09-25 /pmc/articles/PMC6155545/ /pubmed/30252905 http://dx.doi.org/10.1371/journal.pone.0204522 Text en © 2018 Valdés et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Valdés, Alberto
Zhao, Hongxing
Pettersson, Ulf
Lind, Sara Bergström
Time-resolved proteomics of adenovirus infected cells
title Time-resolved proteomics of adenovirus infected cells
title_full Time-resolved proteomics of adenovirus infected cells
title_fullStr Time-resolved proteomics of adenovirus infected cells
title_full_unstemmed Time-resolved proteomics of adenovirus infected cells
title_short Time-resolved proteomics of adenovirus infected cells
title_sort time-resolved proteomics of adenovirus infected cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6155545/
https://www.ncbi.nlm.nih.gov/pubmed/30252905
http://dx.doi.org/10.1371/journal.pone.0204522
work_keys_str_mv AT valdesalberto timeresolvedproteomicsofadenovirusinfectedcells
AT zhaohongxing timeresolvedproteomicsofadenovirusinfectedcells
AT petterssonulf timeresolvedproteomicsofadenovirusinfectedcells
AT lindsarabergstrom timeresolvedproteomicsofadenovirusinfectedcells