Improved functionality of Ligilactobacillus salivarius Li01 in alleviating colonic inflammation by layer-by-layer microencapsulation

Abstract The low viability during gastrointestinal transit and poor mucoadhesion considerably limits the effectiveness of Ligilactobacillus salivarius Li01 (Li01) in regulating gut microbiota and alleviating inflammatory bowel disease (IBD). In this study, a delivery system was designed through laye...

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Autores principales: Mingfei Yao, Yanmeng Lu, Ting Zhang, Jiaojiao Xie, Shengyi Han, Shuobo Zhang, Yiqiu Fei, Zongxin Ling, Jingjing Wu, Yue Hu, Shouling Ji, Hao Chen, Björn Berglund, Lanjuan Li
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Publicado: Nature Portfolio 2021
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spelling oai:doaj.org-article:9855046786c34d518992166806c86a842021-12-02T16:24:50ZImproved functionality of Ligilactobacillus salivarius Li01 in alleviating colonic inflammation by layer-by-layer microencapsulation10.1038/s41522-021-00228-12055-5008https://doaj.org/article/9855046786c34d518992166806c86a842021-07-01T00:00:00Zhttps://doi.org/10.1038/s41522-021-00228-1https://doaj.org/toc/2055-5008Abstract The low viability during gastrointestinal transit and poor mucoadhesion considerably limits the effectiveness of Ligilactobacillus salivarius Li01 (Li01) in regulating gut microbiota and alleviating inflammatory bowel disease (IBD). In this study, a delivery system was designed through layer-by-layer (LbL) encapsulating a single Li01cell with chitosan and alginate. The layers were strengthened by cross-linking to form a firm and mucoadhesive shell (~10 nm thickness) covering the bacterial cell. The LbL Li01 displayed improved viability under simulated gastrointestinal conditions and mucoadhesive function. Almost no cells could be detected among the free Li01 after 2 h incubation in digestive fluids, while for LbL Li01, the total reduction was around 3 log CFU/mL and the viable number of cells remained above 6 log CFU/mL. Besides, a 5-fold increase in the value of rupture length and a two-fold increase in the number of peaks were found in the (bacteria-mucin) adhesion curves of LbL Li01, compared to those of free Li01. Oral administration with LbL Li01 on colitis mice facilitated intestinal barrier recovery and restoration of the gut microbiota. The improved functionality of Li01 by LbL encapsulation could increase the potential for the probiotic to be used in clinical applications to treat IBD; this should be explored in future studies.Mingfei YaoYanmeng LuTing ZhangJiaojiao XieShengyi HanShuobo ZhangYiqiu FeiZongxin LingJingjing WuYue HuShouling JiHao ChenBjörn BerglundLanjuan LiNature PortfolioarticleMicrobial ecologyQR100-130ENnpj Biofilms and Microbiomes, Vol 7, Iss 1, Pp 1-10 (2021)
institution DOAJ
collection DOAJ
language EN
topic Microbial ecology
QR100-130
spellingShingle Microbial ecology
QR100-130
Mingfei Yao
Yanmeng Lu
Ting Zhang
Jiaojiao Xie
Shengyi Han
Shuobo Zhang
Yiqiu Fei
Zongxin Ling
Jingjing Wu
Yue Hu
Shouling Ji
Hao Chen
Björn Berglund
Lanjuan Li
Improved functionality of Ligilactobacillus salivarius Li01 in alleviating colonic inflammation by layer-by-layer microencapsulation
description Abstract The low viability during gastrointestinal transit and poor mucoadhesion considerably limits the effectiveness of Ligilactobacillus salivarius Li01 (Li01) in regulating gut microbiota and alleviating inflammatory bowel disease (IBD). In this study, a delivery system was designed through layer-by-layer (LbL) encapsulating a single Li01cell with chitosan and alginate. The layers were strengthened by cross-linking to form a firm and mucoadhesive shell (~10 nm thickness) covering the bacterial cell. The LbL Li01 displayed improved viability under simulated gastrointestinal conditions and mucoadhesive function. Almost no cells could be detected among the free Li01 after 2 h incubation in digestive fluids, while for LbL Li01, the total reduction was around 3 log CFU/mL and the viable number of cells remained above 6 log CFU/mL. Besides, a 5-fold increase in the value of rupture length and a two-fold increase in the number of peaks were found in the (bacteria-mucin) adhesion curves of LbL Li01, compared to those of free Li01. Oral administration with LbL Li01 on colitis mice facilitated intestinal barrier recovery and restoration of the gut microbiota. The improved functionality of Li01 by LbL encapsulation could increase the potential for the probiotic to be used in clinical applications to treat IBD; this should be explored in future studies.
format article
author Mingfei Yao
Yanmeng Lu
Ting Zhang
Jiaojiao Xie
Shengyi Han
Shuobo Zhang
Yiqiu Fei
Zongxin Ling
Jingjing Wu
Yue Hu
Shouling Ji
Hao Chen
Björn Berglund
Lanjuan Li
author_facet Mingfei Yao
Yanmeng Lu
Ting Zhang
Jiaojiao Xie
Shengyi Han
Shuobo Zhang
Yiqiu Fei
Zongxin Ling
Jingjing Wu
Yue Hu
Shouling Ji
Hao Chen
Björn Berglund
Lanjuan Li
author_sort Mingfei Yao
title Improved functionality of Ligilactobacillus salivarius Li01 in alleviating colonic inflammation by layer-by-layer microencapsulation
title_short Improved functionality of Ligilactobacillus salivarius Li01 in alleviating colonic inflammation by layer-by-layer microencapsulation
title_full Improved functionality of Ligilactobacillus salivarius Li01 in alleviating colonic inflammation by layer-by-layer microencapsulation
title_fullStr Improved functionality of Ligilactobacillus salivarius Li01 in alleviating colonic inflammation by layer-by-layer microencapsulation
title_full_unstemmed Improved functionality of Ligilactobacillus salivarius Li01 in alleviating colonic inflammation by layer-by-layer microencapsulation
title_sort improved functionality of ligilactobacillus salivarius li01 in alleviating colonic inflammation by layer-by-layer microencapsulation
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/9855046786c34d518992166806c86a84
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