Evidence map›Paper›PMID 24682329›Full record

ArticleJournal of bacteriology2014

Streptococcus mutans NADH oxidase lies at the intersection of overlapping regulons controlled by oxygen and NAD+ levels.

J L Baker, A M Derr, K Karuppaiah, M E MacGilvray, J K Kajfasz, R C Faustoferri, I Rivera-Ramos, J P Bitoun, J A Lemos, Z T Wen and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of bacteriology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

40 citing papers in PubMed, 60 citations in OpenAlex.

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  3. Systematic analysis of the glucose-PTS inApplied and environmental microbiology · 2025
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  8. The Dlt and LiaFSR systems derepress SpeB production independently in theFrontiers in cellular and infection microbiology · 2023
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  11. Disruption of theJournal of bacteriology · 2022
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  16. Characterization of the Streptococcus mutansJournal of bacteriology · 2020
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  17. Article
  18. Metallomics : integrated biometal science · 2020
    Article
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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

11 authors at 2 institutions in 1 country.

J L BakerDepartment of Microbiology and Immunology, University of Rochester School of Medicine and Dentistry, Rochester, New York, USA.
A M DerrDepartment of Microbiology and Immunology, University of Rochester School of Medicine and Dentistry, Rochester, New York, USA.
K KaruppaiahCenter for Oral Biology, University of Rochester School of Medicine and Dentistry, Rochester, New York, USA.
M E MacGilvrayCenter for Oral Biology, University of Rochester School of Medicine and Dentistry, Rochester, New York, USA.
J K KajfaszCenter for Oral Biology, University of Rochester School of Medicine and Dentistry, Rochester, New York, USA.
R C FaustoferriCenter for Oral Biology, University of Rochester School of Medicine and Dentistry, Rochester, New York, USA.
I Rivera-RamosDepartment of Microbiology and Immunology, University of Rochester School of Medicine and Dentistry, Rochester, New York, USA.
J P BitounDepartment of Oral and Craniofacial Biology, School of Dentistry, Louisiana State University Health Sciences Center, New Orleans, Louisiana, USA.
J A LemosDepartment of Microbiology and Immunology, University of Rochester School of Medicine and Dentistry, Rochester, New York, USA Center for Oral Biology, University of Rochester School of Medicine and Dentistry, Rochester, New York, USA.
Z T WenDepartment of Oral and Craniofacial Biology, School of Dentistry, Louisiana State University Health Sciences Center, New Orleans, Louisiana, USA.
R G QuiveyDepartment of Microbiology and Immunology, University of Rochester School of Medicine and Dentistry, Rochester, New York, USA Center for Oral Biology, University of Rochester School of Medicine and Dentistry, Rochester, New York, USA Robert_Quivey@urmc.rochester.edu.
University of Rochester · USLouisiana State University Health Sciences Center New Orleans · US

Funding

BrpA in Virulence Modulation of Streptococcus mutansR01DE019452 · NIDCR · LSU HEALTH SCIENCES CENTER · PI ZEZHANG TOM WEN, Hui Wu · 2009 to 2026
$6.3M
Oxidative Stress Responses in Oral StreptococciR01DE013683 · NIDCR · UNIVERSITY OF ROCHESTER · PI QUIVEY, ROBERT G · 2000 to 2019
$6.2M
Training Program in Oral ScienceT90DE021985 · NIDCR · UNIVERSITY OF ROCHESTER · PI OVITT, CATHERINE, YULE, DAVID I · 2011 to 2021
$5.6M
Role of the Spx Regulator in Streptococcus mutansR01DE019783 · NIDCR · UNIVERSITY OF ROCHESTER · PI LEMOS, JOSE A · 2010 to 2020
$3.7M
Fitness profiling of the Streptococcus mutans genomeR01DE017425 · NIDCR · UNIVERSITY OF ROCHESTER · PI QUIVEY, ROBERT G · 2007 to 2011
$3.5M
Training Program in Oral Infectious DiseasesT32DE007165 · NIDCR · UNIVERSITY OF ROCHESTER · PI QUIVEY, ROBERT G · 1985 to 2005
$1.2M
NIDCR NIH HHS DE-019783NIDCR NIH HHS DE-13683NIDCR NIH HHS DE-17425NIDCR NIH HHS DE-19452NIDCR NIH HHS R01 DE013683NIDCR NIH HHS R01 DE017425NIDCR NIH HHS R01 DE019452NIDCR NIH HHS R01 DE019783NIDCR NIH HHS T32 DE007165NIDCR NIH HHS T32 DE-07165NIDCR NIH HHS T90 DE021985NIDCR NIH HHS T90-DE021985
6 · The paper itself

Abstract

NADH oxidase (Nox, encoded by nox) is a flavin-containing enzyme used by the oral pathogen Streptococcus mutans to reduce diatomic oxygen to water while oxidizing NADH to NAD(+). The critical nature of Nox is 2-fold: it serves to regenerate NAD(+), a carbon cycle metabolite, and to reduce intracellular oxygen, preventing formation of destructive reactive oxygen species (ROS). As oxygen and NAD(+) have been shown to modulate the activity of the global transcription factors Spx and Rex, respectively, Nox is potentially poised at a critical junction of two stress regulons. In this study, microarray data showed that either addition of oxygen or loss of nox resulted in altered expression of genes involved in energy metabolism and transport and the upregulation of genes encoding ROS-metabolizing enzymes. Loss of nox also resulted in upregulation of several genes encoding transcription factors and signaling molecules, including the redox-sensing regulator gene rex. Characterization of the nox promoter revealed that nox was regulated by oxygen, through SpxA, and by Rex. These data suggest a regulatory loop in which the roles of nox in reduction of oxygen and regeneration of NAD(+) affect the activity levels of Spx and Rex, respectively, and their regulons, which control several genes, including nox, crucial to growth of S. mutans under conditions of oxidative stress.

Indexed as

Gene DeletionGene Expression Regulation, BacterialGene Expression Regulation, EnzymologicMultienzyme ComplexesNADNADH, NADPH OxidoreductasesOxygenPromoter Regions, GeneticStreptococcus mutansMultienzyme ComplexesNADNADH, NADPH OxidoreductasesNADH oxidaseOxygen

Identifiers

PMID24682329
PMCPMC4054193
OpenAlexW2162234429

What OpenQuestion holds

Textmetadata
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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.