Dual organism transcriptomics of airway epithelial cells interacting with conidia of Aspergillus fumigatus.

Given the complex nature of the responses that can occur in host-pathogen interactions, dual transcriptomics offers a powerful method of elucidating these interactions during infection. The gene expression patterns of Aspergillus fumigatus conidia or host cells have been reported in a number of prev...

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Main Authors: Jean L Oosthuizen, Pol Gomez, Jian Ruan, Tillie L Hackett, Margo M Moore, Darryl A Knight, Scott J Tebbutt
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3105077?pdf=render
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spelling doaj-47fa0891741247b68b25e2f0251503e82020-11-24T21:33:07ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-01-0165e2052710.1371/journal.pone.0020527Dual organism transcriptomics of airway epithelial cells interacting with conidia of Aspergillus fumigatus.Jean L OosthuizenPol GomezJian RuanTillie L HackettMargo M MooreDarryl A KnightScott J TebbuttGiven the complex nature of the responses that can occur in host-pathogen interactions, dual transcriptomics offers a powerful method of elucidating these interactions during infection. The gene expression patterns of Aspergillus fumigatus conidia or host cells have been reported in a number of previous studies, but each focused on only one of the interacting organisms. In the present study, we profiled simultaneously the transcriptional response of both A. fumigatus and human airway epithelial cells (AECs).16HBE14o- transformed bronchial epithelial cells were incubated with A. fumigatus conidia at 37°C for 6 hours, followed by genome-wide transcriptome analysis using human and fungal microarrays. Differentially expressed gene lists were generated from the microarrays, from which biologically relevant themes were identified. Human and fungal candidate genes were selected for validation, using RT-qPCR, in both 16HBE14o- cells and primary AECs co-cultured with conidia.We report that ontologies related to the innate immune response are activated by co-incubation with A. fumigatus condia, and interleukin-6 (IL-6) was confirmed to be up-regulated in primary AECs via RT-qPCR. Concomitantly, A. fumigatus was found to up-regulate fungal pathways involved in iron acquisition, vacuolar acidification, and formate dehydrogenase activity.To our knowledge, this is the first study to apply a dual organism transcriptomics approach to interactions of A. fumigatus conidia and human airway epithelial cells. The up-regulation of IL-6 by epithelia and simultaneous activation of several pathways by fungal conidia warrants further investigation as we seek to better understand this interaction in both health and disease. The cellular response of the airway epithelium to A. fumigatus is important to understand if we are to improve host-pathogen outcomes.http://europepmc.org/articles/PMC3105077?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Jean L Oosthuizen
Pol Gomez
Jian Ruan
Tillie L Hackett
Margo M Moore
Darryl A Knight
Scott J Tebbutt
spellingShingle Jean L Oosthuizen
Pol Gomez
Jian Ruan
Tillie L Hackett
Margo M Moore
Darryl A Knight
Scott J Tebbutt
Dual organism transcriptomics of airway epithelial cells interacting with conidia of Aspergillus fumigatus.
PLoS ONE
author_facet Jean L Oosthuizen
Pol Gomez
Jian Ruan
Tillie L Hackett
Margo M Moore
Darryl A Knight
Scott J Tebbutt
author_sort Jean L Oosthuizen
title Dual organism transcriptomics of airway epithelial cells interacting with conidia of Aspergillus fumigatus.
title_short Dual organism transcriptomics of airway epithelial cells interacting with conidia of Aspergillus fumigatus.
title_full Dual organism transcriptomics of airway epithelial cells interacting with conidia of Aspergillus fumigatus.
title_fullStr Dual organism transcriptomics of airway epithelial cells interacting with conidia of Aspergillus fumigatus.
title_full_unstemmed Dual organism transcriptomics of airway epithelial cells interacting with conidia of Aspergillus fumigatus.
title_sort dual organism transcriptomics of airway epithelial cells interacting with conidia of aspergillus fumigatus.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2011-01-01
description Given the complex nature of the responses that can occur in host-pathogen interactions, dual transcriptomics offers a powerful method of elucidating these interactions during infection. The gene expression patterns of Aspergillus fumigatus conidia or host cells have been reported in a number of previous studies, but each focused on only one of the interacting organisms. In the present study, we profiled simultaneously the transcriptional response of both A. fumigatus and human airway epithelial cells (AECs).16HBE14o- transformed bronchial epithelial cells were incubated with A. fumigatus conidia at 37°C for 6 hours, followed by genome-wide transcriptome analysis using human and fungal microarrays. Differentially expressed gene lists were generated from the microarrays, from which biologically relevant themes were identified. Human and fungal candidate genes were selected for validation, using RT-qPCR, in both 16HBE14o- cells and primary AECs co-cultured with conidia.We report that ontologies related to the innate immune response are activated by co-incubation with A. fumigatus condia, and interleukin-6 (IL-6) was confirmed to be up-regulated in primary AECs via RT-qPCR. Concomitantly, A. fumigatus was found to up-regulate fungal pathways involved in iron acquisition, vacuolar acidification, and formate dehydrogenase activity.To our knowledge, this is the first study to apply a dual organism transcriptomics approach to interactions of A. fumigatus conidia and human airway epithelial cells. The up-regulation of IL-6 by epithelia and simultaneous activation of several pathways by fungal conidia warrants further investigation as we seek to better understand this interaction in both health and disease. The cellular response of the airway epithelium to A. fumigatus is important to understand if we are to improve host-pathogen outcomes.
url http://europepmc.org/articles/PMC3105077?pdf=render
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