Evidence map›Paper›PMID 41652182›Full record

ArticleProbiotics and antimicrobial proteins2026

Gassericins from Lactobacillus Paragasseri K7: Preparative Isolation and Discovery of Dose-Dependent Anti-Inflammatory Effects.

Humna Liaqat, Diana Paveljšek, Jernej Oberčkal, Gabriela Ambrožová, Kristýna Turková, Lukáš Kubala, Adrijana Leonardi, Igor Križaj, Bojana Bogovič Matijašić

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Article in Probiotics and antimicrobial proteins, 2026. 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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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Humna LiaqatDepartment of Animal Science, Biotechnical Faculty, University of Ljubljana, Domžale, 1230, Slovenia.
Diana PaveljšekDepartment of Animal Science, Biotechnical Faculty, University of Ljubljana, Domžale, 1230, Slovenia.
Jernej OberčkalDepartment of Animal Science, Biotechnical Faculty, University of Ljubljana, Domžale, 1230, Slovenia.
Gabriela AmbrožováDepartment of Biophysics of Immune System, Institute of Biophysics of the Czech Academy of Sciences, Brno, Czech Republic.
Kristýna TurkováDepartment of Biophysics of Immune System, Institute of Biophysics of the Czech Academy of Sciences, Brno, Czech Republic.
Lukáš KubalaDepartment of Biophysics of Immune System, Institute of Biophysics of the Czech Academy of Sciences, Brno, Czech Republic.
Adrijana LeonardiDepartment of Molecular and Biomedical Sciences, Jožef Stefan Institute, Ljubljana, 1000, Slovenia.
Igor KrižajDepartment of Molecular and Biomedical Sciences, Jožef Stefan Institute, Ljubljana, 1000, Slovenia.
Bojana Bogovič MatijašićDepartment of Animal Science, Biotechnical Faculty, University of Ljubljana, Domžale, 1230, Slovenia. Bojana.BogovicMatijasic@bf.uni-lj.si.

Funding

National Institute for Research of Metabolic and Cardiovascular Diseases Programme EXCELES, Project No. LX22NPO5104 (Next Generation EU)The Slovenian Research and Innovation Agency Research program P1-0207The Slovenian Research and Innovation Agency Research program P4-0097The Slovenian Research and Innovation Agency Young Researchers' Program (Humna Liaqat, grant number 802-6/2021)
6 · The paper itself

Abstract

Gassericins K7 are heterodimeric bacteriocins produced by Lactobacillus paragasseri K7. Their biological characterisation has been limited by challenges in obtaining these compounds in sufficient purity and quantity. In this study, we used a preparative isolation and purification workflow for gassericins K7, combining ammonium sulphate precipitation, Amberlite XAD-16 extraction, and reversed-phase chromatography. Mass spectrometry confirmed the presence of all four peptide components GasK7A α, GasK7A β, GasK7B α, and GasK7B β in the pooled preparation, including GasK7A β, identified here for the first time in natural isolates of this strain. The purified bacteriocin preparation exhibited strong antibacterial activity against indicator strain Latilactobacillus sakei NCDO 2714. Cytotoxicity testing in RAW 264.7 macrophages revealed minimal effects at concentrations up to 50 µg/ml, with only a modest reduction in cell viability observed at 100 µg/ml. Subsequent evaluation of immunomodulatory properties demonstrated a clear dose-dependent anti-inflammatory effect in LPS-stimulated macrophages. Treatment with gassericins K7 reduced nitric oxide (NO) production, downregulated inducible nitric oxide synthase (iNOS) expression, and suppressed secretion of the pro-inflammatory cytokines TNF-α and IL-6. Importantly, exposure of macrophages to gassericins alone did not elicit any inflammatory response. These findings provide the first evidence of anti-inflammatory activity of purified gassericins K7 in eukaryotic immune cells and highlight their potential as postbiotic components or biotherapeutic candidates for inflammatory disorders. The preparative method used in this study enables the production of gassericins K7 in quantities sufficient for advanced in vitro and in vivo investigations, facilitating future development of bacteriocin-based therapeutics.

Indexed as

Anti-Inflammatory AgentsBacteriocinsLactobacillusAnimalsAnti-Bacterial AgentsCell SurvivalMacrophagesMiceNitric OxideRAW 264.7 CellsAnti-Bacterial AgentsAnti-Inflammatory AgentsBacteriocinsNitric OxideAnti-inflammatory activityBacteriocinsGassericins K7AGassericins K7BImmunomodulationLactobacillus paragasseri K7Purification

Identifiers

PMID41652182
PMCPMC13369773

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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.