Evidence map›Paper›PMID 40540086›Full record

ArticleCurrent microbiology2025

Agar Composition Modulates Production of Trichoderma Peptaibols, Affecting Antibacterial and Antiproliferative Activity.

Patrik Macášek, Adriana Kapustová, Jitka Viktorová, Ján Víglaš, Petra Olejníková, Lukas Grey, Lucia Laubertová, Helena Gbelcová

Abstract read
In one paragraph

Article in Current microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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.

Patrik MacášekFaculty of Medicine, Institute of Medical Biology, Genetics and Clinical Genetics, Comenius University, Sasinkova 4, 811 08, Bratislava, Slovak Republic.
Adriana KapustováFaculty of Medicine, Institute of Medical Biology, Genetics and Clinical Genetics, Comenius University, Sasinkova 4, 811 08, Bratislava, Slovak Republic.
Jitka ViktorováDepartment of Biochemistry and Microbiology, University of Chemistry and Technology Prague, 166 28, Prague, Czech Republic.
Ján VíglašFaculty of Food and Chemical Technology, Institute of Biochemistry and Microbiology, Slovak University of Technology in Bratislava, 812 37, Bratislava, Slovak Republic.
Petra OlejníkováFaculty of Food and Chemical Technology, Institute of Biochemistry and Microbiology, Slovak University of Technology in Bratislava, 812 37, Bratislava, Slovak Republic.
Lukas GreyFaculty of Food and Chemical Technology, Institute of Biochemistry and Microbiology, Slovak University of Technology in Bratislava, 812 37, Bratislava, Slovak Republic.
Lucia LaubertováFaculty of Medicine, Institute of Medical Chemistry, Biochemistry and Clinical Biochemistry, Comenius University, Sasinkova 4, 811 08, Bratislava, Slovak Republic.
Helena GbelcováFaculty of Medicine, Institute of Medical Biology, Genetics and Clinical Genetics, Comenius University, Sasinkova 4, 811 08, Bratislava, Slovak Republic. helena.gbelcova@fmed.uniba.sk.ORCID http://orcid.org/0000-0003-1644-109X

Funding

Agentúra Ministerstva Školstva, Vedy, Výskumu a Športu SR VEGA 1/0388/22Agentúra na Podporu Výskumu a Vývoja APVV-19-0094Ministerstvo Školství, Mládeže a Tělovýchovy INTER-COST LUC24099 (COST Action CA21145 EURESTOP)Univerzita Komenského v Bratislave UK/3211/2024
6 · The paper itself

Abstract

Current antibiotics and chemotherapeutics are becoming ineffective because pathogenic bacteria and tumor cells have developed multiple drug resistance. Therefore, it is necessary to find new substances that can be used in treatment, either alone or as sensitizing molecules in combination with existing drugs. Peptaibols are bioactive, membrane-active peptides of non-ribosomal origin, mainly produced by filamentous fungi such as Trichoderma spp. This study focused on producing peptaibol-rich extracts from Trichoderma atroviride O1, cultivated on malt extract agar (MA) under circadian and constant darkness conditions for 13 days. Peptaibol production was detected by MALDI-TOF mass spectrometry after six days of cultivation. The extracts demonstrated antibacterial activity against Staphylococcus aureus strains, particularly the methicillin-resistant variant, but not against the Gram-negative Pseudomonas aeruginosa. Quorum sensing interference revealed that a peptaibol-rich extract suppressed Vibrio campbellii BAA-1119's AI-2 signaling system to a degree comparable with gentamycin. Beyond antibacterial properties, the extracts exhibited notable antiproliferative activity against human ovarian cancer cells and their adriamycin-resistant subline in both 2D and 3D models. Specifically, MA-derived extracts reduced ovarian cancer cell viability by 70% at 50 μg/mL, especially under light/dark regime of cultivation. Compared to previously published results for PDA-based extracts, MA cultivation shifted the biological effects of peptaibol-containing extracts toward anticancer potential. These findings support the idea that modifying fungal cultivation parameters, the bioactivity of secondary metabolite mixtures can be tailored for specific therapeutic applications.

Indexed as

AgarAnti-Bacterial AgentsAntineoplastic AgentsPeptaibolsTrichodermaCell Line, TumorCell ProliferationCulture MediaHumansHypocrealesMicrobial Sensitivity TestsPseudomonas aeruginosaStaphylococcus aureusAgarAnti-Bacterial AgentsAntineoplastic AgentsCulture MediaPeptaibols

Identifiers

PMID40540086
PMCPMC12181216

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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.