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Modulation of the Gut Microbiota by the Plantaricin-Producing Lactiplantibacillus plantarum D13, Analysed in the DSS-Induced Colitis Mouse Model

Lactiplantibacillus plantarum D13 shows antistaphylococcal and antilisterial activity, probably due to the synthesis of a presumptive bacteriocin with antibiofilm capacity released in the cell-free supernatant (CFS), whose inhibitory effect is enhanced by cocultivation with susceptible strains. An i...

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Autores principales: Butorac, Katarina, Novak, Jasna, Banić, Martina, Leboš Pavunc, Andreja, Čuljak, Nina, Oršolić, Nada, Odeh, Dyana, Perica, Jana, Šušković, Jagoda, Kos, Blaženka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10607255/
https://www.ncbi.nlm.nih.gov/pubmed/37895001
http://dx.doi.org/10.3390/ijms242015322
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author Butorac, Katarina
Novak, Jasna
Banić, Martina
Leboš Pavunc, Andreja
Čuljak, Nina
Oršolić, Nada
Odeh, Dyana
Perica, Jana
Šušković, Jagoda
Kos, Blaženka
author_facet Butorac, Katarina
Novak, Jasna
Banić, Martina
Leboš Pavunc, Andreja
Čuljak, Nina
Oršolić, Nada
Odeh, Dyana
Perica, Jana
Šušković, Jagoda
Kos, Blaženka
author_sort Butorac, Katarina
collection PubMed
description Lactiplantibacillus plantarum D13 shows antistaphylococcal and antilisterial activity, probably due to the synthesis of a presumptive bacteriocin with antibiofilm capacity released in the cell-free supernatant (CFS), whose inhibitory effect is enhanced by cocultivation with susceptible strains. An in silico analysis of the genome of strain D13 confirmed the pln gene cluster. Genes associated with plantaricin biosynthesis, structure, transport, antimicrobial activity, and immunity of strain D13 were identified. Furthermore, the predicted homology-based 3D structures of the cyclic conformation of PlnE, PlnF, PlnJ, and PlnK revealed that PlnE and PlnK contain two helices, while PlnF and PlnJ contain one and two helices, respectively. The potential of the strain to modulate the intestinal microbiota in healthy or dextran sulphate sodium (DSS)-induced colitis mouse models was also investigated. Strain D13 decreased the disease activity index (DAI) and altered the gut microbiota of mice with DSS-induced colitis by increasing the ratio of beneficial microbial species (Allobaculum, Barnesiella) and decreasing those associated with inflammatory bowel disease (Candidatus Saccharimonas). This suggests that strain D13 helps to restore the gut microbiota after DSS-induced colitis, indicating its potential for further investigation as a probiotic strain for the prevention and treatment of colitis.
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spelling pubmed-106072552023-10-28 Modulation of the Gut Microbiota by the Plantaricin-Producing Lactiplantibacillus plantarum D13, Analysed in the DSS-Induced Colitis Mouse Model Butorac, Katarina Novak, Jasna Banić, Martina Leboš Pavunc, Andreja Čuljak, Nina Oršolić, Nada Odeh, Dyana Perica, Jana Šušković, Jagoda Kos, Blaženka Int J Mol Sci Article Lactiplantibacillus plantarum D13 shows antistaphylococcal and antilisterial activity, probably due to the synthesis of a presumptive bacteriocin with antibiofilm capacity released in the cell-free supernatant (CFS), whose inhibitory effect is enhanced by cocultivation with susceptible strains. An in silico analysis of the genome of strain D13 confirmed the pln gene cluster. Genes associated with plantaricin biosynthesis, structure, transport, antimicrobial activity, and immunity of strain D13 were identified. Furthermore, the predicted homology-based 3D structures of the cyclic conformation of PlnE, PlnF, PlnJ, and PlnK revealed that PlnE and PlnK contain two helices, while PlnF and PlnJ contain one and two helices, respectively. The potential of the strain to modulate the intestinal microbiota in healthy or dextran sulphate sodium (DSS)-induced colitis mouse models was also investigated. Strain D13 decreased the disease activity index (DAI) and altered the gut microbiota of mice with DSS-induced colitis by increasing the ratio of beneficial microbial species (Allobaculum, Barnesiella) and decreasing those associated with inflammatory bowel disease (Candidatus Saccharimonas). This suggests that strain D13 helps to restore the gut microbiota after DSS-induced colitis, indicating its potential for further investigation as a probiotic strain for the prevention and treatment of colitis. MDPI 2023-10-18 /pmc/articles/PMC10607255/ /pubmed/37895001 http://dx.doi.org/10.3390/ijms242015322 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Butorac, Katarina
Novak, Jasna
Banić, Martina
Leboš Pavunc, Andreja
Čuljak, Nina
Oršolić, Nada
Odeh, Dyana
Perica, Jana
Šušković, Jagoda
Kos, Blaženka
Modulation of the Gut Microbiota by the Plantaricin-Producing Lactiplantibacillus plantarum D13, Analysed in the DSS-Induced Colitis Mouse Model
title Modulation of the Gut Microbiota by the Plantaricin-Producing Lactiplantibacillus plantarum D13, Analysed in the DSS-Induced Colitis Mouse Model
title_full Modulation of the Gut Microbiota by the Plantaricin-Producing Lactiplantibacillus plantarum D13, Analysed in the DSS-Induced Colitis Mouse Model
title_fullStr Modulation of the Gut Microbiota by the Plantaricin-Producing Lactiplantibacillus plantarum D13, Analysed in the DSS-Induced Colitis Mouse Model
title_full_unstemmed Modulation of the Gut Microbiota by the Plantaricin-Producing Lactiplantibacillus plantarum D13, Analysed in the DSS-Induced Colitis Mouse Model
title_short Modulation of the Gut Microbiota by the Plantaricin-Producing Lactiplantibacillus plantarum D13, Analysed in the DSS-Induced Colitis Mouse Model
title_sort modulation of the gut microbiota by the plantaricin-producing lactiplantibacillus plantarum d13, analysed in the dss-induced colitis mouse model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10607255/
https://www.ncbi.nlm.nih.gov/pubmed/37895001
http://dx.doi.org/10.3390/ijms242015322
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