Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2017
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
_version_ 1782516889978667008
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
work_keys_str_mv AT pannekoekyvonne neisseriameningitidisusessiblingsmallregulatoryrnastoswitchfromcataplerotictoanapleroticmetabolism
AT huisintveldrobertag neisseriameningitidisusessiblingsmallregulatoryrnastoswitchfromcataplerotictoanapleroticmetabolism
AT schipperkim neisseriameningitidisusessiblingsmallregulatoryrnastoswitchfromcataplerotictoanapleroticmetabolism
AT bovenkerksandra neisseriameningitidisusessiblingsmallregulatoryrnastoswitchfromcataplerotictoanapleroticmetabolism
AT kramergertjan neisseriameningitidisusessiblingsmallregulatoryrnastoswitchfromcataplerotictoanapleroticmetabolism
AT brouwermatthijsc neisseriameningitidisusessiblingsmallregulatoryrnastoswitchfromcataplerotictoanapleroticmetabolism
AT vandebeekdiederik neisseriameningitidisusessiblingsmallregulatoryrnastoswitchfromcataplerotictoanapleroticmetabolism
AT speijerdave neisseriameningitidisusessiblingsmallregulatoryrnastoswitchfromcataplerotictoanapleroticmetabolism
AT vanderendearie neisseriameningitidisusessiblingsmallregulatoryrnastoswitchfromcataplerotictoanapleroticmetabolism