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Differential Modulation of Saliva-Derived Microcosm Biofilms by Antimicrobial Peptide LL-31 and D-LL-31

Microbiome modulation, aiming to restore a health-compatible microbiota, is a novel strategy to treat periodontitis. This study evaluated the modulation effects of antimicrobial peptide LL-31 and its D-enantiomer (D-LL-31) on saliva-derived microcosm biofilms, spiked with or without Porphyromonas gi...

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Autores principales: Soldati, Kahena R., Jiang, Yaling, Brandt, Bernd W., Exterkate, Rob A. M., Buijs, Mark J., Nazmi, Kamran, Kaman, Wendy E., Cheng, Lei, Bikker, Floris J., Crielaard, Wim, Zandim-Barcelos, Daniela L., Deng, Dong Mei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10675243/
https://www.ncbi.nlm.nih.gov/pubmed/38003760
http://dx.doi.org/10.3390/pathogens12111295
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author Soldati, Kahena R.
Jiang, Yaling
Brandt, Bernd W.
Exterkate, Rob A. M.
Buijs, Mark J.
Nazmi, Kamran
Kaman, Wendy E.
Cheng, Lei
Bikker, Floris J.
Crielaard, Wim
Zandim-Barcelos, Daniela L.
Deng, Dong Mei
author_facet Soldati, Kahena R.
Jiang, Yaling
Brandt, Bernd W.
Exterkate, Rob A. M.
Buijs, Mark J.
Nazmi, Kamran
Kaman, Wendy E.
Cheng, Lei
Bikker, Floris J.
Crielaard, Wim
Zandim-Barcelos, Daniela L.
Deng, Dong Mei
author_sort Soldati, Kahena R.
collection PubMed
description Microbiome modulation, aiming to restore a health-compatible microbiota, is a novel strategy to treat periodontitis. This study evaluated the modulation effects of antimicrobial peptide LL-31 and its D-enantiomer (D-LL-31) on saliva-derived microcosm biofilms, spiked with or without Porphyromonas gingivalis. To this end, one-day-old biofilms were incubated for 24 h with biofilm medium alone, or medium containing 40 µM LL-31 or D-LL-31, after which biofilms were grown for 5 days. Biofilms were assessed at 1 day and 5 days after intervention for the total viable cell counts, dipeptidyl peptidase IV (DPP4) activity, P. gingivalis amount (by qPCR) and microbial composition (by sequencing). The results showed that D-LL-31, not LL-31, significantly reduced the total viable cell counts, the P. gingivalis amount, and the DPP4 activity of the biofilms spiked with P. gingivalis, but only at 1 day after intervention. In the biofilms spiked with P. gingivalis, D-LL-31 tended to reduce the α-diversity and the compositional shift of the biofilms in time as compared to the control and LL-31 groups. In conclusion, D-LL-31 showed a better performance than LL-31 in biofilm modulation. The biofilm modulation function of the peptides could be impaired when the biofilms were in a severely dysbiotic state.
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spelling pubmed-106752432023-10-29 Differential Modulation of Saliva-Derived Microcosm Biofilms by Antimicrobial Peptide LL-31 and D-LL-31 Soldati, Kahena R. Jiang, Yaling Brandt, Bernd W. Exterkate, Rob A. M. Buijs, Mark J. Nazmi, Kamran Kaman, Wendy E. Cheng, Lei Bikker, Floris J. Crielaard, Wim Zandim-Barcelos, Daniela L. Deng, Dong Mei Pathogens Article Microbiome modulation, aiming to restore a health-compatible microbiota, is a novel strategy to treat periodontitis. This study evaluated the modulation effects of antimicrobial peptide LL-31 and its D-enantiomer (D-LL-31) on saliva-derived microcosm biofilms, spiked with or without Porphyromonas gingivalis. To this end, one-day-old biofilms were incubated for 24 h with biofilm medium alone, or medium containing 40 µM LL-31 or D-LL-31, after which biofilms were grown for 5 days. Biofilms were assessed at 1 day and 5 days after intervention for the total viable cell counts, dipeptidyl peptidase IV (DPP4) activity, P. gingivalis amount (by qPCR) and microbial composition (by sequencing). The results showed that D-LL-31, not LL-31, significantly reduced the total viable cell counts, the P. gingivalis amount, and the DPP4 activity of the biofilms spiked with P. gingivalis, but only at 1 day after intervention. In the biofilms spiked with P. gingivalis, D-LL-31 tended to reduce the α-diversity and the compositional shift of the biofilms in time as compared to the control and LL-31 groups. In conclusion, D-LL-31 showed a better performance than LL-31 in biofilm modulation. The biofilm modulation function of the peptides could be impaired when the biofilms were in a severely dysbiotic state. MDPI 2023-10-29 /pmc/articles/PMC10675243/ /pubmed/38003760 http://dx.doi.org/10.3390/pathogens12111295 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
Soldati, Kahena R.
Jiang, Yaling
Brandt, Bernd W.
Exterkate, Rob A. M.
Buijs, Mark J.
Nazmi, Kamran
Kaman, Wendy E.
Cheng, Lei
Bikker, Floris J.
Crielaard, Wim
Zandim-Barcelos, Daniela L.
Deng, Dong Mei
Differential Modulation of Saliva-Derived Microcosm Biofilms by Antimicrobial Peptide LL-31 and D-LL-31
title Differential Modulation of Saliva-Derived Microcosm Biofilms by Antimicrobial Peptide LL-31 and D-LL-31
title_full Differential Modulation of Saliva-Derived Microcosm Biofilms by Antimicrobial Peptide LL-31 and D-LL-31
title_fullStr Differential Modulation of Saliva-Derived Microcosm Biofilms by Antimicrobial Peptide LL-31 and D-LL-31
title_full_unstemmed Differential Modulation of Saliva-Derived Microcosm Biofilms by Antimicrobial Peptide LL-31 and D-LL-31
title_short Differential Modulation of Saliva-Derived Microcosm Biofilms by Antimicrobial Peptide LL-31 and D-LL-31
title_sort differential modulation of saliva-derived microcosm biofilms by antimicrobial peptide ll-31 and d-ll-31
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10675243/
https://www.ncbi.nlm.nih.gov/pubmed/38003760
http://dx.doi.org/10.3390/pathogens12111295
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