Cargando…
RNA sequencing provides exquisite insight into the manipulation of the alveolar macrophage by tubercle bacilli
Mycobacterium bovis, the agent of bovine tuberculosis, causes an estimated $3 billion annual losses to global agriculture due, in part, to the limitations of current diagnostics. Development of next-generation diagnostics requires a greater understanding of the interaction between the pathogen and t...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4642568/ https://www.ncbi.nlm.nih.gov/pubmed/26346536 http://dx.doi.org/10.1038/srep13629 |
_version_ | 1782400381324623872 |
---|---|
author | Nalpas, Nicolas C. Magee, David A. Conlon, Kevin M. Browne, John A. Healy, Claire McLoughlin, Kirsten E. Rue-Albrecht, Kévin McGettigan, Paul A. Killick, Kate E. Gormley, Eamonn Gordon, Stephen V. MacHugh, David E. |
author_facet | Nalpas, Nicolas C. Magee, David A. Conlon, Kevin M. Browne, John A. Healy, Claire McLoughlin, Kirsten E. Rue-Albrecht, Kévin McGettigan, Paul A. Killick, Kate E. Gormley, Eamonn Gordon, Stephen V. MacHugh, David E. |
author_sort | Nalpas, Nicolas C. |
collection | PubMed |
description | Mycobacterium bovis, the agent of bovine tuberculosis, causes an estimated $3 billion annual losses to global agriculture due, in part, to the limitations of current diagnostics. Development of next-generation diagnostics requires a greater understanding of the interaction between the pathogen and the bovine host. Therefore, to explore the early response of the alveolar macrophage to infection, we report the first application of RNA-sequencing to define, in exquisite detail, the transcriptomes of M. bovis-infected and non-infected alveolar macrophages from ten calves at 2, 6, 24 and 48 hours post-infection. Differentially expressed sense genes were detected at these time points that revealed enrichment of innate immune signalling functions, and transcriptional suppression of host defence mechanisms (e.g., lysosome maturation). We also detected differentially expressed natural antisense transcripts, which may play a role in subverting innate immune mechanisms following infection. Furthermore, we report differential expression of novel bovine genes, some of which have immune-related functions based on orthology with human proteins. This is the first in-depth transcriptomics investigation of the alveolar macrophage response to the early stages of M. bovis infection and reveals complex patterns of gene expression and regulation that underlie the immunomodulatory mechanisms used by M. bovis to evade host defence mechanisms. |
format | Online Article Text |
id | pubmed-4642568 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46425682015-11-20 RNA sequencing provides exquisite insight into the manipulation of the alveolar macrophage by tubercle bacilli Nalpas, Nicolas C. Magee, David A. Conlon, Kevin M. Browne, John A. Healy, Claire McLoughlin, Kirsten E. Rue-Albrecht, Kévin McGettigan, Paul A. Killick, Kate E. Gormley, Eamonn Gordon, Stephen V. MacHugh, David E. Sci Rep Article Mycobacterium bovis, the agent of bovine tuberculosis, causes an estimated $3 billion annual losses to global agriculture due, in part, to the limitations of current diagnostics. Development of next-generation diagnostics requires a greater understanding of the interaction between the pathogen and the bovine host. Therefore, to explore the early response of the alveolar macrophage to infection, we report the first application of RNA-sequencing to define, in exquisite detail, the transcriptomes of M. bovis-infected and non-infected alveolar macrophages from ten calves at 2, 6, 24 and 48 hours post-infection. Differentially expressed sense genes were detected at these time points that revealed enrichment of innate immune signalling functions, and transcriptional suppression of host defence mechanisms (e.g., lysosome maturation). We also detected differentially expressed natural antisense transcripts, which may play a role in subverting innate immune mechanisms following infection. Furthermore, we report differential expression of novel bovine genes, some of which have immune-related functions based on orthology with human proteins. This is the first in-depth transcriptomics investigation of the alveolar macrophage response to the early stages of M. bovis infection and reveals complex patterns of gene expression and regulation that underlie the immunomodulatory mechanisms used by M. bovis to evade host defence mechanisms. Nature Publishing Group 2015-09-08 /pmc/articles/PMC4642568/ /pubmed/26346536 http://dx.doi.org/10.1038/srep13629 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Nalpas, Nicolas C. Magee, David A. Conlon, Kevin M. Browne, John A. Healy, Claire McLoughlin, Kirsten E. Rue-Albrecht, Kévin McGettigan, Paul A. Killick, Kate E. Gormley, Eamonn Gordon, Stephen V. MacHugh, David E. RNA sequencing provides exquisite insight into the manipulation of the alveolar macrophage by tubercle bacilli |
title | RNA sequencing provides exquisite insight into the manipulation of the alveolar macrophage by tubercle bacilli |
title_full | RNA sequencing provides exquisite insight into the manipulation of the alveolar macrophage by tubercle bacilli |
title_fullStr | RNA sequencing provides exquisite insight into the manipulation of the alveolar macrophage by tubercle bacilli |
title_full_unstemmed | RNA sequencing provides exquisite insight into the manipulation of the alveolar macrophage by tubercle bacilli |
title_short | RNA sequencing provides exquisite insight into the manipulation of the alveolar macrophage by tubercle bacilli |
title_sort | rna sequencing provides exquisite insight into the manipulation of the alveolar macrophage by tubercle bacilli |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4642568/ https://www.ncbi.nlm.nih.gov/pubmed/26346536 http://dx.doi.org/10.1038/srep13629 |
work_keys_str_mv | AT nalpasnicolasc rnasequencingprovidesexquisiteinsightintothemanipulationofthealveolarmacrophagebytuberclebacilli AT mageedavida rnasequencingprovidesexquisiteinsightintothemanipulationofthealveolarmacrophagebytuberclebacilli AT conlonkevinm rnasequencingprovidesexquisiteinsightintothemanipulationofthealveolarmacrophagebytuberclebacilli AT brownejohna rnasequencingprovidesexquisiteinsightintothemanipulationofthealveolarmacrophagebytuberclebacilli AT healyclaire rnasequencingprovidesexquisiteinsightintothemanipulationofthealveolarmacrophagebytuberclebacilli AT mcloughlinkirstene rnasequencingprovidesexquisiteinsightintothemanipulationofthealveolarmacrophagebytuberclebacilli AT ruealbrechtkevin rnasequencingprovidesexquisiteinsightintothemanipulationofthealveolarmacrophagebytuberclebacilli AT mcgettiganpaula rnasequencingprovidesexquisiteinsightintothemanipulationofthealveolarmacrophagebytuberclebacilli AT killickkatee rnasequencingprovidesexquisiteinsightintothemanipulationofthealveolarmacrophagebytuberclebacilli AT gormleyeamonn rnasequencingprovidesexquisiteinsightintothemanipulationofthealveolarmacrophagebytuberclebacilli AT gordonstephenv rnasequencingprovidesexquisiteinsightintothemanipulationofthealveolarmacrophagebytuberclebacilli AT machughdavide rnasequencingprovidesexquisiteinsightintothemanipulationofthealveolarmacrophagebytuberclebacilli |