Evidence map›Paper›PMID 38589765›Full record

ArticleJournal of microbiology (Seoul, Korea)2024

Exploring the Therapeutic Potential of Scorpion-Derived Css54 Peptide Against Candida albicans.

Jonggwan Park, Hyeongsun Kim, Da Dam Kang, Yoonkyung Park

Open access · hybridAbstract read
In one paragraph

Article in Journal of microbiology (Seoul, Korea), 2024. 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
2.8field-weighted citation impact, top 10% 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, 8 citations in OpenAlex.

  1. Review
  2. Article
  3. 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

4 authors at 2 institutions in 1 country.

Jonggwan ParkDepartment of Bioinformatics, Kongju National University, Kongju, 32588, Republic of Korea.
Hyeongsun KimDepartment of Biomedical Science, Chosun University, Gwangju, 61452, Republic of Korea.
Da Dam KangDepartment of Biomedical Science, Chosun University, Gwangju, 61452, Republic of Korea.
Yoonkyung ParkDepartment of Biomedical Science, Chosun University, Gwangju, 61452, Republic of Korea. y_k_park@chosun.ac.kr.ORCID http://orcid.org/0000-0002-8717-3080
Chosun University · KRKongju National University · KR

Funding

Institute for Information and Communications Technology Promotion MSIT No. 2017-0-01714National Research Foundation of Korea 2023R1A2C3006368National Research Foundation of Korea NRF-2017M3A9E4077206National Research Foundation of Korea NRF-2021R1C1C2009855National Research Foundation of Korea RS-2023-00228746
6 · The paper itself

Abstract

Candida albicans (C. albicans) is one of the most common opportunistic fungi worldwide, which is associated with a high mortality rate. Despite treatment, C. albicans remains the leading cause of life-threatening invasive infections. Consequently, antimicrobial peptides (AMPs) are potential alternatives as antifungal agents with excellent antifungal activity. We previously reported that Css54, found in the venom of Centrurodies suffusus suffusus (C. s. suffusus) showed antibacterial activity against zoonotic bacteria. However, the antifungal activity of Css54 has not yet been elucidated. The objective of this study was to identify the antifungal activity of Css54 against C. albicans and analyze its mechanism. Css54 showed high antifungal activity against C. albicans. Css54 also inhibited biofilm formation in fluconazole-resistant fungi. The antifungal mechanism of action of Css54 was investigated using membrane-related assays, including the membrane depolarization assay and analysis of the membrane integrity of C. albicans after treatment with Css54. Css54 induced reactive oxygen species (ROS) production in C. albicans, which affected its antifungal activity. Our results indicate that Css54 causes membrane damage in C. albicans, highlighting its value as a potential therapeutic agent against C. albicans infection.

Indexed as

Antifungal AgentsCandida albicansAnimalsBiofilmsFluconazoleMicrobial Sensitivity TestsPeptidesScorpionsAntifungal AgentsFluconazolePeptidesAntifungal activityAntifungal mechanismAntimicrobial peptideCandida albicans

Identifiers

PMID38589765
PMCPMC11021323
OpenAlexW4394580176

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.