Evidence map›Paper›PMID 37946110›Full record

ArticleBMC microbiology2023

Investigating the antimicrobial activity, cytotoxicity, and action mechanism of acylated and amidated derivatives of AurH1 antifungal peptide.

Reyhane Nikookar Golestani, Elahe Ghods, Mosayeb Rostamian, Hamid Madanchi, Ahmad Farhad Talebi

Open access · goldAbstract read
In one paragraph

Article in BMC microbiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Novel Isoxazole-Based Antifungal Drug Candidates.International journal of molecular sciences · 2024
    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 4 institutions in 1 country.

Reyhane Nikookar GolestaniDepartment of Microbial Biotechnology, Faculty of New Sciences and Technologies, Semnan University, Semnan, 35131-19111, Iran.
Elahe GhodsDepartment of Biotechnology, School of Medicine, Semnan University of Medical Sciences, Semnan, 35131-38111, Iran.
Mosayeb RostamianInfectious Diseases Research Center, Health Institute, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Hamid MadanchiDepartment of Biotechnology, School of Medicine, Semnan University of Medical Sciences, Semnan, 35131-38111, Iran. hamidmadanchi@yahoo.com.ORCID 0000-0002-6527-7321
Ahmad Farhad TalebiDepartment of Microbial Biotechnology, Faculty of New Sciences and Technologies, Semnan University, Semnan, 35131-19111, Iran. aftalebi@semnan.ac.ir.
Semnan University · IRKermanshah University of Medical Sciences · IRPasteur Institute of Iran · IRSemnan University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe increasing growth of microbial resistance threatens the health of human societies. Therefore, the discovery and design of new antibiotics seem necessary. Today, antimicrobial peptides (AMPs) are receiving attention due to their unique properties. In our previous studies, exclusive antifungal effects of AurH1, which is a truncated and modified form of Aurein1.2, were synthesized. In this study, AurH1 antifungal peptide was synthesized into acylated (Ac-AurH1) and amidated (AurH1-NH

resultsThe results showed that amidation at the C-terminal of AurH1 compared to acylation at the N-terminal of it can improve the antifungal properties and cytotoxicity of AurH1. The results showed that AurH1 amidation can maintain the antifungal activity of this peptide in the culture medium containing specific dilutions of human serum compared to the intact AurH1. Also, the amidation of the C-terminal of AurH1 could not affect the mechanism of action and its time -of killing.

conclusionAs a result, the amidation of the C-terminal of the AurH1 is a suitable strategy to improve its antifungal properties and cytotoxicity. This modification can enhance its properties for animal studies.

Indexed as

Antifungal AgentsAnti-Infective AgentsAnimalsAnti-Bacterial AgentsHumansMicrobial Sensitivity TestsPeptidesAnti-Bacterial AgentsAntifungal AgentsAnti-Infective AgentsPeptidesAcylationAmidationAntifungal peptidesAntimicrobial peptidesAurein1.2AurH1

Identifiers

PMID37946110
PMCPMC10633902
OpenAlexW4388520383

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.