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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...

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Autores principales: Ackland, Jodie, Heinson, Ashley I., Cleary, David W., Christodoulides, Myron, Wilkinson, Tom M. A., Staples, Karl J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
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.
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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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