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Marine Microalgae, Spirulina maxima-Derived Modified Pectin and Modified Pectin Nanoparticles Modulate the Gut Microbiota and Trigger Immune Responses in Mice

This study evaluated the modulation of gut microbiota, immune responses, and gut morphometry in C57BL/6 mice, upon oral administration of S. maxima-derived modified pectin (SmP, 7.5 mg/mL) and pectin nanoparticles (SmPNPs; 7.5 mg/mL). Metagenomics analysis was conducted using fecal samples, and mice...

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Autores principales: Chandrarathna, H.P.S.U., Liyanage, T.D., Edirisinghe, S.L., Dananjaya, S.H.S., Thulshan, E.H.T., Nikapitiya, Chamilani, Oh, Chulhong, Kang, Do-Hyung, De Zoysa, Mahanama
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7143556/
https://www.ncbi.nlm.nih.gov/pubmed/32245246
http://dx.doi.org/10.3390/md18030175
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author Chandrarathna, H.P.S.U.
Liyanage, T.D.
Edirisinghe, S.L.
Dananjaya, S.H.S.
Thulshan, E.H.T.
Nikapitiya, Chamilani
Oh, Chulhong
Kang, Do-Hyung
De Zoysa, Mahanama
author_facet Chandrarathna, H.P.S.U.
Liyanage, T.D.
Edirisinghe, S.L.
Dananjaya, S.H.S.
Thulshan, E.H.T.
Nikapitiya, Chamilani
Oh, Chulhong
Kang, Do-Hyung
De Zoysa, Mahanama
author_sort Chandrarathna, H.P.S.U.
collection PubMed
description This study evaluated the modulation of gut microbiota, immune responses, and gut morphometry in C57BL/6 mice, upon oral administration of S. maxima-derived modified pectin (SmP, 7.5 mg/mL) and pectin nanoparticles (SmPNPs; 7.5 mg/mL). Metagenomics analysis was conducted using fecal samples, and mice duodenum and jejunum were used for analyzing the immune response and gut morphometry, respectively. The results of metagenomics analysis revealed that the abundance of Bacteroidetes in the gut increased in response to both modified SmP and SmPNPs (75%) as compared with that in the control group (66%), while that of Firmicutes decreased in (20%) as compared with that in the control group (30%). The mRNA levels of mucin, antimicrobial peptide, and antiviral and gut permeability-related genes in the duodenum were significantly (p < 0.05) upregulated (> 2-fold) upon modified SmP and SmPNPs feeding. Protein level of intestinal alkaline phosphatase was increased (1.9-fold) in the duodenum of modified SmPNPs feeding, evidenced by significantly increased goblet cell density (0.5 ± 0.03 cells/1000 µm(2)) and villi height (352 ± 10 µm). Our results suggest that both modified SmP and SmPNPs have the potential to modulate gut microbial community, enhance the expression of immune related genes, and improve gut morphology.
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spelling pubmed-71435562020-04-14 Marine Microalgae, Spirulina maxima-Derived Modified Pectin and Modified Pectin Nanoparticles Modulate the Gut Microbiota and Trigger Immune Responses in Mice Chandrarathna, H.P.S.U. Liyanage, T.D. Edirisinghe, S.L. Dananjaya, S.H.S. Thulshan, E.H.T. Nikapitiya, Chamilani Oh, Chulhong Kang, Do-Hyung De Zoysa, Mahanama Mar Drugs Article This study evaluated the modulation of gut microbiota, immune responses, and gut morphometry in C57BL/6 mice, upon oral administration of S. maxima-derived modified pectin (SmP, 7.5 mg/mL) and pectin nanoparticles (SmPNPs; 7.5 mg/mL). Metagenomics analysis was conducted using fecal samples, and mice duodenum and jejunum were used for analyzing the immune response and gut morphometry, respectively. The results of metagenomics analysis revealed that the abundance of Bacteroidetes in the gut increased in response to both modified SmP and SmPNPs (75%) as compared with that in the control group (66%), while that of Firmicutes decreased in (20%) as compared with that in the control group (30%). The mRNA levels of mucin, antimicrobial peptide, and antiviral and gut permeability-related genes in the duodenum were significantly (p < 0.05) upregulated (> 2-fold) upon modified SmP and SmPNPs feeding. Protein level of intestinal alkaline phosphatase was increased (1.9-fold) in the duodenum of modified SmPNPs feeding, evidenced by significantly increased goblet cell density (0.5 ± 0.03 cells/1000 µm(2)) and villi height (352 ± 10 µm). Our results suggest that both modified SmP and SmPNPs have the potential to modulate gut microbial community, enhance the expression of immune related genes, and improve gut morphology. MDPI 2020-03-21 /pmc/articles/PMC7143556/ /pubmed/32245246 http://dx.doi.org/10.3390/md18030175 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Chandrarathna, H.P.S.U.
Liyanage, T.D.
Edirisinghe, S.L.
Dananjaya, S.H.S.
Thulshan, E.H.T.
Nikapitiya, Chamilani
Oh, Chulhong
Kang, Do-Hyung
De Zoysa, Mahanama
Marine Microalgae, Spirulina maxima-Derived Modified Pectin and Modified Pectin Nanoparticles Modulate the Gut Microbiota and Trigger Immune Responses in Mice
title Marine Microalgae, Spirulina maxima-Derived Modified Pectin and Modified Pectin Nanoparticles Modulate the Gut Microbiota and Trigger Immune Responses in Mice
title_full Marine Microalgae, Spirulina maxima-Derived Modified Pectin and Modified Pectin Nanoparticles Modulate the Gut Microbiota and Trigger Immune Responses in Mice
title_fullStr Marine Microalgae, Spirulina maxima-Derived Modified Pectin and Modified Pectin Nanoparticles Modulate the Gut Microbiota and Trigger Immune Responses in Mice
title_full_unstemmed Marine Microalgae, Spirulina maxima-Derived Modified Pectin and Modified Pectin Nanoparticles Modulate the Gut Microbiota and Trigger Immune Responses in Mice
title_short Marine Microalgae, Spirulina maxima-Derived Modified Pectin and Modified Pectin Nanoparticles Modulate the Gut Microbiota and Trigger Immune Responses in Mice
title_sort marine microalgae, spirulina maxima-derived modified pectin and modified pectin nanoparticles modulate the gut microbiota and trigger immune responses in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7143556/
https://www.ncbi.nlm.nih.gov/pubmed/32245246
http://dx.doi.org/10.3390/md18030175
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