Evidence map›Paper›PMID 24509501›Full record

ArticleMicrobiology (Reading, England)2014

β-Phosphoglucomutase contributes to aciduricity in Streptococcus mutans.

Andrew A Buckley, Roberta C Faustoferri, Robert G Quivey

Abstract read
In one paragraph

Article in Microbiology (Reading, England), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

14 citing papers in PubMed, 18 citations in OpenAlex.

  1. Microorganisms · 2023
    Review
  2. Article
  3. The Route of Sucrose Utilization byFrontiers in microbiology · 2021
    Article
  4. Article
  5. Article
  6. [Role of SMU.2055 gene in regulating acid resistance of Streptococcus mutans UA159].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2018
    Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
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

3 authors at 1 institution in 1 country.

Andrew A BuckleyDepartment of Microbiology & Immunology, University of Rochester School of Medicine and Dentistry, Rochester, NY 14642, USA.
Roberta C FaustoferriCenter for Oral Biology, University of Rochester School of Medicine and Dentistry, Rochester, NY 14642, USA.
Robert G QuiveyCenter for Oral Biology, University of Rochester School of Medicine and Dentistry, Rochester, NY 14642, USA.
University of Rochester · US

Funding

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
Fitness profiling of the Streptococcus mutans genomeR01DE017425 · NIDCR · UNIVERSITY OF ROCHESTER · PI QUIVEY, ROBERT G · 2007 to 2011
$3.5M
Low pH-mediated membrane biosynthesis in S. mutans.R01DE017157 · NIDCR · UNIVERSITY OF ROCHESTER · PI QUIVEY, ROBERT G · 2006 to 2010
$1.8M
Training Program in Oral Infectious DiseasesT32DE007165 · NIDCR · UNIVERSITY OF ROCHESTER · PI QUIVEY, ROBERT G · 1985 to 2005
$1.2M
NIDCR NIH HHS DE-13683NIDCR NIH HHS DE- 17157NIDCR NIH HHS DE-17425NIDCR NIH HHS R01 DE013683NIDCR NIH HHS R01 DE017425NIDCR NIH HHS T32 DE007165NIDCR NIH HHS T32 DE-07165NIDCR NIH HHS T90 DE021985NIDCR NIH HHS T90-DE021985
6 · The paper itself

Abstract

Streptococcus mutans encounters an array of sugar moieties within the oral cavity due to a varied human diet. One such sugar is β-d-glucose 1-phosphate (βDG1P), which must be converted to glucose 6-phosphate (G6P) before further metabolism to lactic acid. The conversion of βDG1P to G6P is mediated by β-phosphoglucomutase, which has not been previously observed in any oral streptococci, but has been extensively characterized and the gene designated pgmB in Lactococcus lactis. An orthologue was identified in S. mutans, SMU.1747c, and deletion of the gene resulted in the inability of the deletion strain to convert βDG1P to G6P, indicating that SMU.1747c is a β-phosphoglucomutase and should be designated pgmB. In this study, we sought to characterize how deletion of pgmB affected known virulence factors of S. mutans, specifically acid tolerance. The ΔpgmB strain showed a decreased ability to survive acid challenge. Additionally, the strain lacking β-phosphoglucomutase had a diminished glycolytic profile compared with the parental strain. Deletion of pgmB had a negative impact on the virulence of S. mutans in the Galleria mellonella (greater wax worm) animal model. Our results indicate that pgmB plays a role at the juncture of carbohydrate metabolism and virulence.

Indexed as

AcidsAnimalsDisease Models, AnimalGene DeletionGlucose-6-PhosphateGlucosephosphatesLepidopteraMicrobial ViabilityPhosphoglucomutaseStreptococcal InfectionsStreptococcus mutansVirulenceVirulence FactorsAcidsglucose-1-phosphateGlucose-6-PhosphateGlucosephosphatesPhosphoglucomutaseVirulence Factors

Identifiers

PMID24509501
PMCPMC3973451
OpenAlexW2146459311

What OpenQuestion holds

Textmetadata
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.