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Global transcriptional responses of pneumococcus to human blood components and cerebrospinal fluid

Streptococcus pneumoniae (pneumococcus) is a leading cause of severe invasive infectious diseases such as sepsis and meningitis. Understanding how pneumococcus adapts and survive in the human bloodstream environment and cerebrospinal fluid (CSF) is important for development of future treatment strat...

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Autores principales: Pettersen, Jens Sivkær, Høg, Frida Fabricius, Nielsen, Flemming Damgaard, Møller-Jensen, Jakob, Jørgensen, Mikkel Girke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9812572/
https://www.ncbi.nlm.nih.gov/pubmed/36620004
http://dx.doi.org/10.3389/fmicb.2022.1060583
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author Pettersen, Jens Sivkær
Høg, Frida Fabricius
Nielsen, Flemming Damgaard
Møller-Jensen, Jakob
Jørgensen, Mikkel Girke
author_facet Pettersen, Jens Sivkær
Høg, Frida Fabricius
Nielsen, Flemming Damgaard
Møller-Jensen, Jakob
Jørgensen, Mikkel Girke
author_sort Pettersen, Jens Sivkær
collection PubMed
description Streptococcus pneumoniae (pneumococcus) is a leading cause of severe invasive infectious diseases such as sepsis and meningitis. Understanding how pneumococcus adapts and survive in the human bloodstream environment and cerebrospinal fluid (CSF) is important for development of future treatment strategies. This study investigates the global transcriptional response of pneumococcus to human blood components and CSF acquired from discarded and anonymized patient samples. Extensive transcriptional changes to human blood components were observed during early stages of interaction. Plasma-specific responses were primarily related to metabolic components and include strong downregulation of fatty acid biosynthesis genes, and upregulation of nucleotide biosynthesis genes. No transcriptional responses specific to the active plasma proteins (e.g., complement proteins) were observed during early stages of interaction as demonstrated by a differential expression analysis between plasma and heat-inactivated plasma. The red blood cell (RBC)-specific response was far more complex, and included activation of the competence system, differential expression of several two-component systems, phosphotransferase systems and transition metal transporter genes. Interestingly, most of the changes observed for CSF were also observed for plasma. One of the few CSF-specific responses, not observed for plasma, was a strong downregulation of the iron acquisition system piuBCDA. Intriguingly, this transcriptomic analysis also uncovers significant differential expression of more than 20 small non-coding RNAs, most of them in response to RBCs, including small RNAs from uncharacterized type I toxin-antitoxin systems. In summary, this transcriptomic study identifies key pneumococcal metabolic pathways and regulatory genes involved with adaptation to human blood and CSF. Future studies should uncover the potential involvement of these factors with virulence in-vivo.
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spelling pubmed-98125722023-01-05 Global transcriptional responses of pneumococcus to human blood components and cerebrospinal fluid Pettersen, Jens Sivkær Høg, Frida Fabricius Nielsen, Flemming Damgaard Møller-Jensen, Jakob Jørgensen, Mikkel Girke Front Microbiol Microbiology Streptococcus pneumoniae (pneumococcus) is a leading cause of severe invasive infectious diseases such as sepsis and meningitis. Understanding how pneumococcus adapts and survive in the human bloodstream environment and cerebrospinal fluid (CSF) is important for development of future treatment strategies. This study investigates the global transcriptional response of pneumococcus to human blood components and CSF acquired from discarded and anonymized patient samples. Extensive transcriptional changes to human blood components were observed during early stages of interaction. Plasma-specific responses were primarily related to metabolic components and include strong downregulation of fatty acid biosynthesis genes, and upregulation of nucleotide biosynthesis genes. No transcriptional responses specific to the active plasma proteins (e.g., complement proteins) were observed during early stages of interaction as demonstrated by a differential expression analysis between plasma and heat-inactivated plasma. The red blood cell (RBC)-specific response was far more complex, and included activation of the competence system, differential expression of several two-component systems, phosphotransferase systems and transition metal transporter genes. Interestingly, most of the changes observed for CSF were also observed for plasma. One of the few CSF-specific responses, not observed for plasma, was a strong downregulation of the iron acquisition system piuBCDA. Intriguingly, this transcriptomic analysis also uncovers significant differential expression of more than 20 small non-coding RNAs, most of them in response to RBCs, including small RNAs from uncharacterized type I toxin-antitoxin systems. In summary, this transcriptomic study identifies key pneumococcal metabolic pathways and regulatory genes involved with adaptation to human blood and CSF. Future studies should uncover the potential involvement of these factors with virulence in-vivo. Frontiers Media S.A. 2022-12-21 /pmc/articles/PMC9812572/ /pubmed/36620004 http://dx.doi.org/10.3389/fmicb.2022.1060583 Text en Copyright © 2022 Pettersen, Høg, Nielsen, Møller-Jensen and Jørgensen. 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 Microbiology
Pettersen, Jens Sivkær
Høg, Frida Fabricius
Nielsen, Flemming Damgaard
Møller-Jensen, Jakob
Jørgensen, Mikkel Girke
Global transcriptional responses of pneumococcus to human blood components and cerebrospinal fluid
title Global transcriptional responses of pneumococcus to human blood components and cerebrospinal fluid
title_full Global transcriptional responses of pneumococcus to human blood components and cerebrospinal fluid
title_fullStr Global transcriptional responses of pneumococcus to human blood components and cerebrospinal fluid
title_full_unstemmed Global transcriptional responses of pneumococcus to human blood components and cerebrospinal fluid
title_short Global transcriptional responses of pneumococcus to human blood components and cerebrospinal fluid
title_sort global transcriptional responses of pneumococcus to human blood components and cerebrospinal fluid
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9812572/
https://www.ncbi.nlm.nih.gov/pubmed/36620004
http://dx.doi.org/10.3389/fmicb.2022.1060583
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