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L-Arginine Destabilizes Oral Multi-Species Biofilm Communities Developed in Human Saliva

The amino acid L-arginine inhibits bacterial coaggregation, is involved in cell-cell signaling, and alters bacterial metabolism in a broad range of species present in the human oral cavity. Given the range of effects of L-arginine on bacteria, we hypothesized that L-arginine might alter multi-specie...

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Autores principales: Kolderman, Ethan, Bettampadi, Deepti, Samarian, Derek, Dowd, Scot E., Foxman, Betsy, Jakubovics, Nicholas S., Rickard, Alexander H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4422691/
https://www.ncbi.nlm.nih.gov/pubmed/25946040
http://dx.doi.org/10.1371/journal.pone.0121835
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author Kolderman, Ethan
Bettampadi, Deepti
Samarian, Derek
Dowd, Scot E.
Foxman, Betsy
Jakubovics, Nicholas S.
Rickard, Alexander H.
author_facet Kolderman, Ethan
Bettampadi, Deepti
Samarian, Derek
Dowd, Scot E.
Foxman, Betsy
Jakubovics, Nicholas S.
Rickard, Alexander H.
author_sort Kolderman, Ethan
collection PubMed
description The amino acid L-arginine inhibits bacterial coaggregation, is involved in cell-cell signaling, and alters bacterial metabolism in a broad range of species present in the human oral cavity. Given the range of effects of L-arginine on bacteria, we hypothesized that L-arginine might alter multi-species oral biofilm development and cause developed multi-species biofilms to disassemble. Because of these potential biofilm-destabilizing effects, we also hypothesized that L-arginine might enhance the efficacy of antimicrobials that normally cannot rapidly penetrate biofilms. A static microplate biofilm system and a controlled-flow microfluidic system were used to develop multi-species oral biofilms derived from pooled unfiltered cell-containing saliva (CCS) in pooled filter-sterilized cell-free saliva (CFS) at 37(o)C. The addition of pH neutral L-arginine monohydrochloride (LAHCl) to CFS was found to exert negligible antimicrobial effects but significantly altered biofilm architecture in a concentration-dependent manner. Under controlled flow, the biovolume of biofilms (μm(3)/μm(2)) developed in saliva containing 100-500 mM LAHCl were up to two orders of magnitude less than when developed without LAHCI. Culture-independent community analysis demonstrated that 500 mM LAHCl substantially altered biofilm species composition: the proportion of Streptococcus and Veillonella species increased and the proportion of Gram-negative bacteria such as Neisseria and Aggregatibacter species was reduced. Adding LAHCl to pre-formed biofilms also reduced biovolume, presumably by altering cell-cell interactions and causing cell detachment. Furthermore, supplementing 0.01% cetylpyridinium chloride (CPC), an antimicrobial commonly used for the treatment of dental plaque, with 500 mM LAHCl resulted in greater penetration of CPC into the biofilms and significantly greater killing compared to a non-supplemented 0.01% CPC solution. Collectively, this work demonstrates that LAHCl moderates multi-species oral biofilm development and community composition and enhances the activity of CPC. The incorporation of LAHCl into oral healthcare products may be useful for enhanced biofilm control.
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spelling pubmed-44226912015-05-12 L-Arginine Destabilizes Oral Multi-Species Biofilm Communities Developed in Human Saliva Kolderman, Ethan Bettampadi, Deepti Samarian, Derek Dowd, Scot E. Foxman, Betsy Jakubovics, Nicholas S. Rickard, Alexander H. PLoS One Research Article The amino acid L-arginine inhibits bacterial coaggregation, is involved in cell-cell signaling, and alters bacterial metabolism in a broad range of species present in the human oral cavity. Given the range of effects of L-arginine on bacteria, we hypothesized that L-arginine might alter multi-species oral biofilm development and cause developed multi-species biofilms to disassemble. Because of these potential biofilm-destabilizing effects, we also hypothesized that L-arginine might enhance the efficacy of antimicrobials that normally cannot rapidly penetrate biofilms. A static microplate biofilm system and a controlled-flow microfluidic system were used to develop multi-species oral biofilms derived from pooled unfiltered cell-containing saliva (CCS) in pooled filter-sterilized cell-free saliva (CFS) at 37(o)C. The addition of pH neutral L-arginine monohydrochloride (LAHCl) to CFS was found to exert negligible antimicrobial effects but significantly altered biofilm architecture in a concentration-dependent manner. Under controlled flow, the biovolume of biofilms (μm(3)/μm(2)) developed in saliva containing 100-500 mM LAHCl were up to two orders of magnitude less than when developed without LAHCI. Culture-independent community analysis demonstrated that 500 mM LAHCl substantially altered biofilm species composition: the proportion of Streptococcus and Veillonella species increased and the proportion of Gram-negative bacteria such as Neisseria and Aggregatibacter species was reduced. Adding LAHCl to pre-formed biofilms also reduced biovolume, presumably by altering cell-cell interactions and causing cell detachment. Furthermore, supplementing 0.01% cetylpyridinium chloride (CPC), an antimicrobial commonly used for the treatment of dental plaque, with 500 mM LAHCl resulted in greater penetration of CPC into the biofilms and significantly greater killing compared to a non-supplemented 0.01% CPC solution. Collectively, this work demonstrates that LAHCl moderates multi-species oral biofilm development and community composition and enhances the activity of CPC. The incorporation of LAHCl into oral healthcare products may be useful for enhanced biofilm control. Public Library of Science 2015-05-06 /pmc/articles/PMC4422691/ /pubmed/25946040 http://dx.doi.org/10.1371/journal.pone.0121835 Text en © 2015 Kolderman et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Kolderman, Ethan
Bettampadi, Deepti
Samarian, Derek
Dowd, Scot E.
Foxman, Betsy
Jakubovics, Nicholas S.
Rickard, Alexander H.
L-Arginine Destabilizes Oral Multi-Species Biofilm Communities Developed in Human Saliva
title L-Arginine Destabilizes Oral Multi-Species Biofilm Communities Developed in Human Saliva
title_full L-Arginine Destabilizes Oral Multi-Species Biofilm Communities Developed in Human Saliva
title_fullStr L-Arginine Destabilizes Oral Multi-Species Biofilm Communities Developed in Human Saliva
title_full_unstemmed L-Arginine Destabilizes Oral Multi-Species Biofilm Communities Developed in Human Saliva
title_short L-Arginine Destabilizes Oral Multi-Species Biofilm Communities Developed in Human Saliva
title_sort l-arginine destabilizes oral multi-species biofilm communities developed in human saliva
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4422691/
https://www.ncbi.nlm.nih.gov/pubmed/25946040
http://dx.doi.org/10.1371/journal.pone.0121835
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