Evidence map›Paper›PMID 36412172›Full record

ArticleMolecular oral microbiology2023

Characterization of FA1654: A putative DPS protein in Filifactor alocis.

Malissa Mangar, Arunima Mishra, Zhengrong Yang, Champion Deivanayagam, Hansel M Fletcher

Open access · hybridAbstract read
In one paragraph

Article in Molecular oral microbiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 36% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Functional Characterization of a Putative Sortase FA1364 inInternational journal of molecular sciences · 2026
    Article
  2. Article
  3. 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

5 authors at 2 institutions in 1 country.

Malissa MangarDivision of Microbiology & Molecular Genetics, School of Medicine, Loma Linda University, Loma Linda, California, USA.
Arunima MishraDivision of Microbiology & Molecular Genetics, School of Medicine, Loma Linda University, Loma Linda, California, USA.
Zhengrong YangDepartment of Biochemistry and Molecular Genetics, University of Alabama, Birmingham, Alabama, USA.
Champion DeivanayagamDepartment of Biochemistry and Molecular Genetics, University of Alabama, Birmingham, Alabama, USA.
Hansel M FletcherDivision of Microbiology & Molecular Genetics, School of Medicine, Loma Linda University, Loma Linda, California, USA.ORCID 0000-0002-7165-2159
Loma Linda University · USUniversity of Alabama at Birmingham · US

Funding

Studies on the virulence regulation in PorphyromonasR01DE025852 · NIDCR · LOMA LINDA UNIVERSITY · PI FLETCHER, HANSEL M. · 2016 to 2020
$2.0M
Mechanisms for the repair of oxidative stress-induced DNA damage in PorphyromonasR21DE030411 · NIDCR · LOMA LINDA UNIVERSITY · PI FLETCHER, HANSEL M. · 2021 to 2022
$435k
Oxidative Stress Resistance Mechanisms in Filifactor AlocisR03DE029825 · NIDCR · LOMA LINDA UNIVERSITY · PI MISHRA, ARUNIMA · 2021 to 2022
$316k
NIDCR NIH HHS R01 DE025852NIDCR NIH HHS R03 DE029825NIDCR NIH HHS R21 DE030411
6 · The paper itself

Abstract

The survival/adaptation of Filifactor alocis, a fastidious Gram-positive asaccharolytic anaerobe, to the inflammatory environment of the periodontal pocket requires an ability to overcome oxidative stress. Moreover, its pathogenic characteristics are highlighted by its capacity to survive in the oxidative-stress microenvironment of the periodontal pocket and a likely ability to modulate the microbial community dynamics. There is still a significant gap in our understanding of its mechanism of oxidative stress resistance and its impact on the virulence and pathogenicity of the microbial biofilm. Coinfection of epithelial cells with F. alocis and Porphyromonas gingivalis resulted in the upregulation of several genes, including HMPREF0389_01654 (FA1654). Bioinformatics analysis indicates that FA1654 has a "di-iron binding domain" and could function as a DNA starvation and stationary phase protection (DPS) protein. We have further characterized the FA1654 protein to determine its role in oxidative stress resistance in F. alocis. In the presence of hydrogen peroxide-induced oxidative stress, there was an ∼1.3 fold upregulation of the FA1654 gene in F. alocis. Incubation of the purified FA1654 protein with DNA in the presence of hydrogen peroxide and iron resulted in the protection of the DNA from Fenton-mediated degradation. Circular dichroism and differential scanning fluorimetry studies have documented the intrinsic ability of rFA1654 protein to bind iron; however, the rFA1654 protein is missing the intrinsic ability to reduce hydrogen peroxide. Collectively, the data may suggest that FA1654 in F. alocis is involved in oxidative stress resistance via an ability to protect against Fenton-mediated oxidative stress-induced damage.

Indexed as

EubacterialesHydrogen PeroxideEpithelial CellsHumansPeriodontal PocketHydrogen PeroxideDPS proteinFenton reactionFilifactor alocisoxidative stressperiodontal disease

Identifiers

PMID36412172
PMCPMC9905271
OpenAlexW4309656088

What OpenQuestion holds

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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.