Differential Modulation of Saliva-Derived Microcosm Biofilms by Antimicrobial Peptide LL-31 and D-LL-31
| dc.contributor.author | Soldati, Kahena R. [UNESP] | |
| dc.contributor.author | Jiang, Yaling | |
| dc.contributor.author | Brandt, Bernd W. | |
| dc.contributor.author | Exterkate, Rob A. M. | |
| dc.contributor.author | Buijs, Mark J. | |
| dc.contributor.author | Nazmi, Kamran | |
| dc.contributor.author | Kaman, Wendy E. | |
| dc.contributor.author | Cheng, Lei | |
| dc.contributor.author | Bikker, Floris J. | |
| dc.contributor.author | Crielaard, Wim | |
| dc.contributor.author | Zandim-Barcelos, Daniela L. [UNESP] | |
| dc.contributor.author | Deng, Dong Mei | |
| dc.contributor.institution | University of Amsterdam and Vrije Universiteit Amsterdam | |
| dc.contributor.institution | Universidade Estadual Paulista (UNESP) | |
| dc.contributor.institution | Sichuan University | |
| dc.date.accessioned | 2025-04-29T18:07:28Z | |
| dc.date.issued | 2023-11-01 | |
| dc.description.abstract | 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. | en |
| dc.description.affiliation | Department of Preventive Dentistry Academic Center for Dentistry Amsterdam (ACTA) University of Amsterdam and Vrije Universiteit Amsterdam, LA | |
| dc.description.affiliation | Department of Oral Diagnosis and Surgery School of Dentistry at Araraquara Universidade Estadual Paulista—UNESP, SP | |
| dc.description.affiliation | State Key Laboratory of Oral Diseases & National Center for Stomatology & National Clinical Research Center for Oral Diseases & Department of Operative Dentistry and Endodontics West China Hospital of Stomatology Sichuan University | |
| dc.description.affiliation | Department of Oral Biochemistry Academic Centre for Dentistry Amsterdam (ACTA) University of Amsterdam and Vrije Universiteit Amsterdam | |
| dc.description.affiliationUnesp | Department of Oral Diagnosis and Surgery School of Dentistry at Araraquara Universidade Estadual Paulista—UNESP, SP | |
| dc.identifier | http://dx.doi.org/10.3390/pathogens12111295 | |
| dc.identifier.citation | Pathogens, v. 12, n. 11, 2023. | |
| dc.identifier.doi | 10.3390/pathogens12111295 | |
| dc.identifier.issn | 2076-0817 | |
| dc.identifier.scopus | 2-s2.0-85178316230 | |
| dc.identifier.uri | https://hdl.handle.net/11449/297702 | |
| dc.language.iso | eng | |
| dc.relation.ispartof | Pathogens | |
| dc.source | Scopus | |
| dc.subject | 16S rRNA gene amplicon sequencing | |
| dc.subject | oral microbiome | |
| dc.subject | periodontitis | |
| dc.subject | Porphyromonas gingivalis | |
| dc.subject | saliva-derived microcosm biofilms | |
| dc.title | Differential Modulation of Saliva-Derived Microcosm Biofilms by Antimicrobial Peptide LL-31 and D-LL-31 | en |
| dc.type | Artigo | pt |
| dspace.entity.type | Publication | |
| relation.isOrgUnitOfPublication | ca4c0298-cd82-48ee-a9c8-c97704bac2b0 | |
| relation.isOrgUnitOfPublication.latestForDiscovery | ca4c0298-cd82-48ee-a9c8-c97704bac2b0 | |
| unesp.author.orcid | 0000-0002-1155-1989[3] | |
| unesp.author.orcid | 0000-0002-6472-3051[4] | |
| unesp.author.orcid | 0000-0002-0159-2816[7] | |
| unesp.author.orcid | 0000-0002-2762-4740[8] | |
| unesp.author.orcid | 0000-0002-9453-4630[9] | |
| unesp.author.orcid | 0000-0003-3706-1678[12] | |
| unesp.campus | Universidade Estadual Paulista (UNESP), Faculdade de Odontologia, Araraquara | pt |

