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RNA thermosensors facilitate Streptococcus pneumoniae and Haemophilus influenzae immune evasion
Bacterial meningitis is a major cause of death and disability in children worldwide. Two human restricted respiratory pathogens, Streptococcus pneumoniae and Haemophilus influenzae, are the major causative agents of bacterial meningitis, attributing to 200,000 deaths annually. These pathogens are of...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8084184/ https://www.ncbi.nlm.nih.gov/pubmed/33914847 http://dx.doi.org/10.1371/journal.ppat.1009513 |
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author | Eichner, Hannes Karlsson, Jens Spelmink, Laura Pathak, Anuj Sham, Lok-To Henriques-Normark, Birgitta Loh, Edmund |
author_facet | Eichner, Hannes Karlsson, Jens Spelmink, Laura Pathak, Anuj Sham, Lok-To Henriques-Normark, Birgitta Loh, Edmund |
author_sort | Eichner, Hannes |
collection | PubMed |
description | Bacterial meningitis is a major cause of death and disability in children worldwide. Two human restricted respiratory pathogens, Streptococcus pneumoniae and Haemophilus influenzae, are the major causative agents of bacterial meningitis, attributing to 200,000 deaths annually. These pathogens are often part of the nasopharyngeal microflora of healthy carriers. However, what factors elicit them to disseminate and cause invasive diseases, remain unknown. Elevated temperature and fever are hallmarks of inflammation triggered by infections and can act as warning signals to pathogens. Here, we investigate whether these respiratory pathogens can sense environmental temperature to evade host complement-mediated killing. We show that productions of two vital virulence factors and vaccine components, the polysaccharide capsules and factor H binding proteins, are temperature dependent, thus influencing serum/opsonophagocytic killing of the bacteria. We identify and characterise four novel RNA thermosensors in S. pneumoniae and H. influenzae, responsible for capsular biosynthesis and production of factor H binding proteins. Our data suggest that these bacteria might have independently co-evolved thermosensing abilities with different RNA sequences but distinct secondary structures to evade the immune system. |
format | Online Article Text |
id | pubmed-8084184 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-80841842021-05-06 RNA thermosensors facilitate Streptococcus pneumoniae and Haemophilus influenzae immune evasion Eichner, Hannes Karlsson, Jens Spelmink, Laura Pathak, Anuj Sham, Lok-To Henriques-Normark, Birgitta Loh, Edmund PLoS Pathog Research Article Bacterial meningitis is a major cause of death and disability in children worldwide. Two human restricted respiratory pathogens, Streptococcus pneumoniae and Haemophilus influenzae, are the major causative agents of bacterial meningitis, attributing to 200,000 deaths annually. These pathogens are often part of the nasopharyngeal microflora of healthy carriers. However, what factors elicit them to disseminate and cause invasive diseases, remain unknown. Elevated temperature and fever are hallmarks of inflammation triggered by infections and can act as warning signals to pathogens. Here, we investigate whether these respiratory pathogens can sense environmental temperature to evade host complement-mediated killing. We show that productions of two vital virulence factors and vaccine components, the polysaccharide capsules and factor H binding proteins, are temperature dependent, thus influencing serum/opsonophagocytic killing of the bacteria. We identify and characterise four novel RNA thermosensors in S. pneumoniae and H. influenzae, responsible for capsular biosynthesis and production of factor H binding proteins. Our data suggest that these bacteria might have independently co-evolved thermosensing abilities with different RNA sequences but distinct secondary structures to evade the immune system. Public Library of Science 2021-04-29 /pmc/articles/PMC8084184/ /pubmed/33914847 http://dx.doi.org/10.1371/journal.ppat.1009513 Text en © 2021 Eichner et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Eichner, Hannes Karlsson, Jens Spelmink, Laura Pathak, Anuj Sham, Lok-To Henriques-Normark, Birgitta Loh, Edmund RNA thermosensors facilitate Streptococcus pneumoniae and Haemophilus influenzae immune evasion |
title | RNA thermosensors facilitate Streptococcus pneumoniae and Haemophilus influenzae immune evasion |
title_full | RNA thermosensors facilitate Streptococcus pneumoniae and Haemophilus influenzae immune evasion |
title_fullStr | RNA thermosensors facilitate Streptococcus pneumoniae and Haemophilus influenzae immune evasion |
title_full_unstemmed | RNA thermosensors facilitate Streptococcus pneumoniae and Haemophilus influenzae immune evasion |
title_short | RNA thermosensors facilitate Streptococcus pneumoniae and Haemophilus influenzae immune evasion |
title_sort | rna thermosensors facilitate streptococcus pneumoniae and haemophilus influenzae immune evasion |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8084184/ https://www.ncbi.nlm.nih.gov/pubmed/33914847 http://dx.doi.org/10.1371/journal.ppat.1009513 |
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