Evidence map›Paper›PMID 25946040›Full record

ArticlePloS one2015

L-arginine destabilizes oral multi-species biofilm communities developed in human saliva.

Ethan Kolderman, Deepti Bettampadi, Derek Samarian, Scot E Dowd, Betsy Foxman, Nicholas S Jakubovics, Alexander H Rickard

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
9.2field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

58 citing papers in PubMed, 107 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Ethan KoldermanCenter for Molecular and Clinical Epidemiology of Infectious Diseases, Department of Epidemiology, University of Michigan, Ann Arbor, MI, United States of America.
Deepti BettampadiCenter for Molecular and Clinical Epidemiology of Infectious Diseases, Department of Epidemiology, University of Michigan, Ann Arbor, MI, United States of America.
Derek SamarianCenter for Molecular and Clinical Epidemiology of Infectious Diseases, Department of Epidemiology, University of Michigan, Ann Arbor, MI, United States of America.
Scot E DowdMolecular Research LP (MR DNA), Shallowater, TX, United States of America.
Betsy FoxmanCenter for Molecular and Clinical Epidemiology of Infectious Diseases, Department of Epidemiology, University of Michigan, Ann Arbor, MI, United States of America.
Nicholas S JakubovicsCentre for Oral Health Research, School of Dental Sciences, Newcastle University, Newcastle upon Tyne, NE2 4BW, United States of America.
Alexander H RickardCenter for Molecular and Clinical Epidemiology of Infectious Diseases, Department of Epidemiology, University of Michigan, Ann Arbor, MI, United States of America.
University of Michigan–Ann Arbor · USMassanutten Regional Library · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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° 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.

Indexed as

Anti-Bacterial AgentsArginineBiofilmsHumansMicrobiotaSalivaAnti-Bacterial AgentsArginine

Identifiers

PMID25946040
PMCPMC4422691
OpenAlexW312996121

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.