The University of Southampton
University of Southampton Institutional Repository

Denitrification in human dental plaque

Denitrification in human dental plaque
Denitrification in human dental plaque
Background
Microbial denitrification is not considered important in human-associated microbial communities. Accordingly, metabolic investigations of the microbial biofilm communities of human dental plaque have focused on aerobic respiration and acid fermentation of carbohydrates, even though it is known that the oral habitat is constantly exposed to nitrate (NO3-) concentrations in the millimolar range and that dental plaque houses bacteria that can reduce this NO3- to nitrite (NO2-).

Results
We show that dental plaque mediates denitrification of NO3- to nitric oxide (NO), nitrous oxide (N2O), and dinitrogen (N2) using microsensor measurements, 15N isotopic labelling and molecular detection of denitrification genes. In vivo N2O accumulation rates in the mouth depended on the presence of dental plaque and on salivary NO3- concentrations. NO and N2O production by denitrification occurred under aerobic conditions and was regulated by plaque pH.

Conclusions
Increases of NO concentrations were in the range of effective concentrations for NO signalling to human host cells and, thus, may locally affect blood flow, signalling between nerves and inflammatory processes in the gum. This is specifically significant for the understanding of periodontal diseases, where NO has been shown to play a key role, but where gingival cells are believed to be the only source of NO. More generally, this study establishes denitrification by human-associated microbial communities as a significant metabolic pathway which, due to concurrent NO formation, provides a basis for symbiotic interactions.
Denitrification as a source for nitric oxide and nitrous oxide in human dental plaque
1741-7007
Schreiber, F.
bd04e7b2-fb42-468c-a09c-11729bb0cc38
Stief, P.
8b8a637f-01c7-4fc9-82b7-b12ac614202e
Gieseke, A.
9e64f3c8-aced-493d-8efc-e9868dcb04d0
Heisterkampa, I.
f91c96e0-71d6-4ad1-b7b3-b8e16ed587ef
Verstraete, W.
6f6ed0a8-1b27-4f65-96f4-4a345fb054f1
DeBeer, D.
78a5fcaa-e0f4-413b-83b9-97f7281b3055
Stoodley, P.
08614665-92a9-4466-806e-20c6daeb483f
Schreiber, F.
bd04e7b2-fb42-468c-a09c-11729bb0cc38
Stief, P.
8b8a637f-01c7-4fc9-82b7-b12ac614202e
Gieseke, A.
9e64f3c8-aced-493d-8efc-e9868dcb04d0
Heisterkampa, I.
f91c96e0-71d6-4ad1-b7b3-b8e16ed587ef
Verstraete, W.
6f6ed0a8-1b27-4f65-96f4-4a345fb054f1
DeBeer, D.
78a5fcaa-e0f4-413b-83b9-97f7281b3055
Stoodley, P.
08614665-92a9-4466-806e-20c6daeb483f

Schreiber, F., Stief, P., Gieseke, A., Heisterkampa, I., Verstraete, W., DeBeer, D. and Stoodley, P. (2010) Denitrification in human dental plaque. BMC Biology, 8 (24). (doi:10.1186/1741-7007-8-24).

Record type: Article

Abstract

Background
Microbial denitrification is not considered important in human-associated microbial communities. Accordingly, metabolic investigations of the microbial biofilm communities of human dental plaque have focused on aerobic respiration and acid fermentation of carbohydrates, even though it is known that the oral habitat is constantly exposed to nitrate (NO3-) concentrations in the millimolar range and that dental plaque houses bacteria that can reduce this NO3- to nitrite (NO2-).

Results
We show that dental plaque mediates denitrification of NO3- to nitric oxide (NO), nitrous oxide (N2O), and dinitrogen (N2) using microsensor measurements, 15N isotopic labelling and molecular detection of denitrification genes. In vivo N2O accumulation rates in the mouth depended on the presence of dental plaque and on salivary NO3- concentrations. NO and N2O production by denitrification occurred under aerobic conditions and was regulated by plaque pH.

Conclusions
Increases of NO concentrations were in the range of effective concentrations for NO signalling to human host cells and, thus, may locally affect blood flow, signalling between nerves and inflammatory processes in the gum. This is specifically significant for the understanding of periodontal diseases, where NO has been shown to play a key role, but where gingival cells are believed to be the only source of NO. More generally, this study establishes denitrification by human-associated microbial communities as a significant metabolic pathway which, due to concurrent NO formation, provides a basis for symbiotic interactions.

This record has no associated files available for download.

More information

Published date: April 2010
Additional Information: The National Centre for Advanced Tribology at Southampton (nCATS)
Keywords: Denitrification as a source for nitric oxide and nitrous oxide in human dental plaque
Organisations: Engineering Mats & Surface Engineerg Gp

Identifiers

Local EPrints ID: 71665
URI: http://eprints.soton.ac.uk/id/eprint/71665
ISSN: 1741-7007
PURE UUID: f4c7b1bd-0b10-4268-aedc-34d286bd8792
ORCID for P. Stoodley: ORCID iD orcid.org/0000-0001-6069-273X

Catalogue record

Date deposited: 17 Dec 2009
Last modified: 14 Mar 2024 02:55

Export record

Altmetrics

Contributors

Author: F. Schreiber
Author: P. Stief
Author: A. Gieseke
Author: I. Heisterkampa
Author: W. Verstraete
Author: D. DeBeer
Author: P. Stoodley ORCID iD

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×