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Dual RNASeq Reveals NTHi-Macrophage Transcriptomic Changes During Intracellular Persistence
Nontypeable Haemophilus influenzae (NTHi) is a pathobiont which chronically colonises the airway of individuals with chronic respiratory disease and is associated with poor clinical outcomes. It is unclear how NTHi persists in the airway, however accumulating evidence suggests that NTHi can invade a...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8419319/ https://www.ncbi.nlm.nih.gov/pubmed/34497778 http://dx.doi.org/10.3389/fcimb.2021.723481 |
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author | Ackland, Jodie Heinson, Ashley I. Cleary, David W. Christodoulides, Myron Wilkinson, Tom M. A. Staples, Karl J. |
author_facet | Ackland, Jodie Heinson, Ashley I. Cleary, David W. Christodoulides, Myron Wilkinson, Tom M. A. Staples, Karl J. |
author_sort | Ackland, Jodie |
collection | PubMed |
description | Nontypeable Haemophilus influenzae (NTHi) is a pathobiont which chronically colonises the airway of individuals with chronic respiratory disease and is associated with poor clinical outcomes. It is unclear how NTHi persists in the airway, however accumulating evidence suggests that NTHi can invade and persist within macrophages. To better understand the mechanisms of NTHi persistence within macrophages, we developed an in vitro model of NTHi intracellular persistence using human monocyte-derived macrophages (MDM). Dual RNA Sequencing was used to assess MDM and NTHi transcriptomic regulation occurring simultaneously during NTHi persistence. Analysis of the macrophage response to NTHi identified temporally regulated transcriptomic profiles, with a specific ‘core’ profile displaying conserved expression of genes across time points. Gene list enrichment analysis identified enrichment of immune responses in the core gene set, with KEGG pathway analysis revealing specific enrichment of intracellular immune response pathways. NTHi persistence was facilitated by modulation of bacterial metabolic, stress response and ribosome pathways. Levels of NTHi genes bioC, mepM and dps were differentially expressed by intracellular NTHi compared to planktonic NTHi, indicating that the transcriptomic adaption was distinct between the two different NTHi lifestyles. Overall, this study provides crucial insights into the transcriptomic adaptations facilitating NTHi persistence within macrophages. Targeting these reported pathways with novel therapeutics to reduce NTHi burden in the airway could be an effective treatment strategy given the current antimicrobial resistance crisis and lack of NTHi vaccines. |
format | Online Article Text |
id | pubmed-8419319 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84193192021-09-07 Dual RNASeq Reveals NTHi-Macrophage Transcriptomic Changes During Intracellular Persistence Ackland, Jodie Heinson, Ashley I. Cleary, David W. Christodoulides, Myron Wilkinson, Tom M. A. Staples, Karl J. Front Cell Infect Microbiol Cellular and Infection Microbiology Nontypeable Haemophilus influenzae (NTHi) is a pathobiont which chronically colonises the airway of individuals with chronic respiratory disease and is associated with poor clinical outcomes. It is unclear how NTHi persists in the airway, however accumulating evidence suggests that NTHi can invade and persist within macrophages. To better understand the mechanisms of NTHi persistence within macrophages, we developed an in vitro model of NTHi intracellular persistence using human monocyte-derived macrophages (MDM). Dual RNA Sequencing was used to assess MDM and NTHi transcriptomic regulation occurring simultaneously during NTHi persistence. Analysis of the macrophage response to NTHi identified temporally regulated transcriptomic profiles, with a specific ‘core’ profile displaying conserved expression of genes across time points. Gene list enrichment analysis identified enrichment of immune responses in the core gene set, with KEGG pathway analysis revealing specific enrichment of intracellular immune response pathways. NTHi persistence was facilitated by modulation of bacterial metabolic, stress response and ribosome pathways. Levels of NTHi genes bioC, mepM and dps were differentially expressed by intracellular NTHi compared to planktonic NTHi, indicating that the transcriptomic adaption was distinct between the two different NTHi lifestyles. Overall, this study provides crucial insights into the transcriptomic adaptations facilitating NTHi persistence within macrophages. Targeting these reported pathways with novel therapeutics to reduce NTHi burden in the airway could be an effective treatment strategy given the current antimicrobial resistance crisis and lack of NTHi vaccines. Frontiers Media S.A. 2021-08-23 /pmc/articles/PMC8419319/ /pubmed/34497778 http://dx.doi.org/10.3389/fcimb.2021.723481 Text en Copyright © 2021 Ackland, Heinson, Cleary, Christodoulides, Wilkinson and Staples https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cellular and Infection Microbiology Ackland, Jodie Heinson, Ashley I. Cleary, David W. Christodoulides, Myron Wilkinson, Tom M. A. Staples, Karl J. Dual RNASeq Reveals NTHi-Macrophage Transcriptomic Changes During Intracellular Persistence |
title | Dual RNASeq Reveals NTHi-Macrophage Transcriptomic Changes During Intracellular Persistence |
title_full | Dual RNASeq Reveals NTHi-Macrophage Transcriptomic Changes During Intracellular Persistence |
title_fullStr | Dual RNASeq Reveals NTHi-Macrophage Transcriptomic Changes During Intracellular Persistence |
title_full_unstemmed | Dual RNASeq Reveals NTHi-Macrophage Transcriptomic Changes During Intracellular Persistence |
title_short | Dual RNASeq Reveals NTHi-Macrophage Transcriptomic Changes During Intracellular Persistence |
title_sort | dual rnaseq reveals nthi-macrophage transcriptomic changes during intracellular persistence |
topic | Cellular and Infection Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8419319/ https://www.ncbi.nlm.nih.gov/pubmed/34497778 http://dx.doi.org/10.3389/fcimb.2021.723481 |
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