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抗菌肽LL-31和D-LL-31对唾液来源的微生态生物膜的差异调节作用

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

作者信息

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

机构信息

Department of Preventive Dentistry, Academic Center for Dentistry Amsterdam (ACTA), University of Amsterdam and Vrije Universiteit Amsterdam, 1081 LA Amsterdam, The Netherlands.

Department of Oral Diagnosis and Surgery, School of Dentistry at Araraquara, Universidade Estadual Paulista-UNESP, Araraquara 1680, SP, Brazil.

出版信息

Pathogens. 2023 Oct 29;12(11):1295. doi: 10.3390/pathogens12111295.

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 . 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, 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 amount, and the DPP4 activity of the biofilms spiked with , but only at 1 day after intervention. In the biofilms spiked with , 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.

摘要

微生物群调节旨在恢复与健康相容的微生物群,是一种治疗牙周炎的新策略。本研究评估了抗菌肽LL-31及其D-对映体(D-LL-31)对添加或未添加[具体物质未给出]的唾液衍生微生态生物膜的调节作用。为此,将一天龄的生物膜分别与单独的生物膜培养基、含有40µM LL-31或D-LL-31的培养基孵育24小时,之后让生物膜生长5天。在干预后的第1天和第5天评估生物膜的总活细胞计数、二肽基肽酶IV(DPP4)活性、[具体物质未给出]量(通过定量聚合酶链反应)和微生物组成(通过测序)。结果表明,D-LL-31而非LL-31能显著降低添加[具体物质未给出]的生物膜的总活细胞计数、[具体物质未给出]量和DPP4活性,但仅在干预后的第1天。在添加[具体物质未给出]的生物膜中,与对照组和LL-31组相比,D-LL-31随着时间推移倾向于降低生物膜的α多样性和组成变化。总之,在生物膜调节方面,D-LL-31表现优于LL-31。当生物膜处于严重失调状态时,这些肽的生物膜调节功能可能会受损。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c09c/10675243/6df70500ffe8/pathogens-12-01295-g001.jpg

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