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Neisseria meningitidis Uses Sibling Small Regulatory RNAs To Switch from Cataplerotic to Anaplerotic Metabolism
Neisseria meningitidis (the meningococcus) is primarily a commensal of the human oropharynx that sporadically causes septicemia and meningitis. Meningococci adapt to diverse local host conditions differing in nutrient supply, like the nasopharynx, blood, and cerebrospinal fluid, by changing metaboli...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5362039/ https://www.ncbi.nlm.nih.gov/pubmed/28325760 http://dx.doi.org/10.1128/mBio.02293-16 |
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author | Pannekoek, Yvonne Huis in ‘t Veld, Robert A. G. Schipper, Kim Bovenkerk, Sandra Kramer, Gertjan Brouwer, Matthijs C. van de Beek, Diederik Speijer, Dave van der Ende, Arie |
author_facet | Pannekoek, Yvonne Huis in ‘t Veld, Robert A. G. Schipper, Kim Bovenkerk, Sandra Kramer, Gertjan Brouwer, Matthijs C. van de Beek, Diederik Speijer, Dave van der Ende, Arie |
author_sort | Pannekoek, Yvonne |
collection | PubMed |
description | Neisseria meningitidis (the meningococcus) is primarily a commensal of the human oropharynx that sporadically causes septicemia and meningitis. Meningococci adapt to diverse local host conditions differing in nutrient supply, like the nasopharynx, blood, and cerebrospinal fluid, by changing metabolism and protein repertoire. However, regulatory transcription factors and two-component systems in meningococci involved in adaptation to local nutrient variations are limited. We identified novel sibling small regulatory RNAs (Neisseria metabolic switch regulators [NmsRs]) regulating switches between cataplerotic and anaplerotic metabolism in this pathogen. Overexpression of NmsRs was tolerated in blood but not in cerebrospinal fluid. Expression of six tricarboxylic acid cycle enzymes was downregulated by direct action of NmsRs. Expression of the NmsRs themselves was under the control of the stringent response through the action of RelA. Small sibling regulatory RNAs of meningococci, controlling general metabolic switches, add an exciting twist to their versatile repertoire in bacterial pathogens. |
format | Online Article Text |
id | pubmed-5362039 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-53620392017-03-24 Neisseria meningitidis Uses Sibling Small Regulatory RNAs To Switch from Cataplerotic to Anaplerotic Metabolism Pannekoek, Yvonne Huis in ‘t Veld, Robert A. G. Schipper, Kim Bovenkerk, Sandra Kramer, Gertjan Brouwer, Matthijs C. van de Beek, Diederik Speijer, Dave van der Ende, Arie mBio Research Article Neisseria meningitidis (the meningococcus) is primarily a commensal of the human oropharynx that sporadically causes septicemia and meningitis. Meningococci adapt to diverse local host conditions differing in nutrient supply, like the nasopharynx, blood, and cerebrospinal fluid, by changing metabolism and protein repertoire. However, regulatory transcription factors and two-component systems in meningococci involved in adaptation to local nutrient variations are limited. We identified novel sibling small regulatory RNAs (Neisseria metabolic switch regulators [NmsRs]) regulating switches between cataplerotic and anaplerotic metabolism in this pathogen. Overexpression of NmsRs was tolerated in blood but not in cerebrospinal fluid. Expression of six tricarboxylic acid cycle enzymes was downregulated by direct action of NmsRs. Expression of the NmsRs themselves was under the control of the stringent response through the action of RelA. Small sibling regulatory RNAs of meningococci, controlling general metabolic switches, add an exciting twist to their versatile repertoire in bacterial pathogens. American Society for Microbiology 2017-03-21 /pmc/articles/PMC5362039/ /pubmed/28325760 http://dx.doi.org/10.1128/mBio.02293-16 Text en Copyright © 2017 Pannekoek et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Pannekoek, Yvonne Huis in ‘t Veld, Robert A. G. Schipper, Kim Bovenkerk, Sandra Kramer, Gertjan Brouwer, Matthijs C. van de Beek, Diederik Speijer, Dave van der Ende, Arie Neisseria meningitidis Uses Sibling Small Regulatory RNAs To Switch from Cataplerotic to Anaplerotic Metabolism |
title | Neisseria meningitidis Uses Sibling Small Regulatory RNAs To Switch from Cataplerotic to Anaplerotic Metabolism |
title_full | Neisseria meningitidis Uses Sibling Small Regulatory RNAs To Switch from Cataplerotic to Anaplerotic Metabolism |
title_fullStr | Neisseria meningitidis Uses Sibling Small Regulatory RNAs To Switch from Cataplerotic to Anaplerotic Metabolism |
title_full_unstemmed | Neisseria meningitidis Uses Sibling Small Regulatory RNAs To Switch from Cataplerotic to Anaplerotic Metabolism |
title_short | Neisseria meningitidis Uses Sibling Small Regulatory RNAs To Switch from Cataplerotic to Anaplerotic Metabolism |
title_sort | neisseria meningitidis uses sibling small regulatory rnas to switch from cataplerotic to anaplerotic metabolism |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5362039/ https://www.ncbi.nlm.nih.gov/pubmed/28325760 http://dx.doi.org/10.1128/mBio.02293-16 |
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