Evidence map›Paper›PMID 27549081›Full record

ArticleBMC microbiology2016

Novel cationic peptide TP359 down-regulates the expression of outer membrane biogenesis genes in Pseudomonas aeruginosa: a potential TP359 anti-microbial mechanism.

Ejovwoke F Dosunmu, Atul A Chaudhari, Swapnil Bawage, Mona K Bakeer, Donald R Owen, Shree R Singh, Vida A Dennis, Shreekumar R Pillai

Open access · goldAbstract read
In one paragraph

Article in BMC microbiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

5 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Antimicrobial Mechanism of pBD2 againstMolecules (Basel, Switzerland) · 2020
    Article
  3. Article
  4. Article
  5. Review
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

8 authors at 3 institutions in 1 country.

Ejovwoke F DosunmuCenter for NanoBiotechnology Research, Alabama State University, Montgomery, AL, USA.
Atul A ChaudhariCenter for NanoBiotechnology Research, Alabama State University, Montgomery, AL, USA.
Swapnil BawageCenter for NanoBiotechnology Research, Alabama State University, Montgomery, AL, USA.
Mona K BakeerLSU Health Sciences Center, School of Allied Health Professions, New Orleans, LA, USA.
Donald R OwenTherapeutic Peptides Inc., Baton Rouge, LA, USA.
Shree R SinghCenter for NanoBiotechnology Research, Alabama State University, Montgomery, AL, USA.
Vida A DennisCenter for NanoBiotechnology Research, Alabama State University, Montgomery, AL, USA.
Shreekumar R PillaiCenter for NanoBiotechnology Research, Alabama State University, Montgomery, AL, USA. spillai@alasu.edu.
Alabama State University · USLouisiana State University Health Sciences Center New Orleans · USPeptides International (United States) · US

Funding

RISE Option II:NIGMS-Research Initiative for Scientific Enhancement (RISE) Program at ASUR25GM106995 · NIGMS · ALABAMA STATE UNIVERSITY · PI DENNIS, VIDA A · 2013 to 2023
$3.0M
NIGMS NIH HHS R25 GM106995
6 · The paper itself

Abstract

backgroundAntimicrobial peptides (AMPs) are a class of antimicrobial agents with broad-spectrum activities. Several reports indicate that cationic AMPs bind to the negatively charged bacterial membrane causing membrane depolarization and damage. However, membrane depolarization and damage may be insufficient to elicit cell death, thereby suggesting that other mechanism(s) of action could be involved in this phenomenon. In this study, we investigated the antimicrobial activity of a novel antimicrobial peptide, TP359, against two strains of Pseudomonas aeruginosa, as well as its possible mechanisms of action.

resultsTP359 proved to be bactericidal against P. aeruginosa as confirmed by the reduced bacteria counts, membrane damage and cytoplasmic membrane depolarization. In addition, it was non-toxic to mouse J774 macrophages and human lung A549 epithelial cells. Electron microscopy analysis showed TP359 bactericidal effects by structural changes of the bacteria from viable rod-shaped cells to those with cell membrane damages, proceeding into the efflux of cytoplasmic contents and emergence of ghost cells. Gene expression analysis on the effects of TP359 on outer membrane biogenesis genes underscored marked down-regulation, particularly of oprF, which encodes a major structural and outer membrane porin (OprF) in both strains studied, indicating that the peptide may cause deregulation of outer membrane genes and reduced structural stability which could lead to cell death.

conclusionOur data shows that TP359 has potent antimicrobial activity against P aeruginosa. The correlation between membrane damage, depolarization and reduced expression of outer membrane biogenesis genes, particularly oprF may suggest the bactericidal mechanism of action of the TP359 peptide.

Indexed as

A549 CellsAnimalsAnti-Bacterial AgentsAntimicrobial Cationic PeptidesBacterial Outer Membrane ProteinsBacterial ProteinsCell LineCell MembraneCell Membrane PermeabilityDown-RegulationHumansMacrophagesMiceMicrobial Sensitivity TestsPorinsPseudomonas aeruginosaAnti-Bacterial AgentsAntimicrobial Cationic PeptidesBacterial Outer Membrane ProteinsBacterial ProteinsOprF protein, Pseudomonas aeruginosaPorinsAntimicrobial effectAntimicrobial peptidesPseudomonas aeruginosa

Identifiers

PMID27549081
PMCPMC4994277
OpenAlexW2510344382

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.