Cargando…
Efficient protection of microorganisms for delivery to the intestinal tract by cellulose sulphate encapsulation
BACKGROUND: Gut microbiota in humans and animals play an important role in health, aiding in digestion, regulation of the immune system and protection against pathogens. Changes or imbalances in the gut microbiota (dysbiosis) have been linked to a variety of local and systemic diseases, and there is...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7691082/ https://www.ncbi.nlm.nih.gov/pubmed/33243224 http://dx.doi.org/10.1186/s12934-020-01465-3 |
_version_ | 1783614213019664384 |
---|---|
author | Gunzburg, Walter H. Aung, Myo Myint Toa, Pauline Ng, Shirelle Read, Eliot Tan, Wee Jin Brandtner, Eva Maria Dangerfield, John Salmons, Brian |
author_facet | Gunzburg, Walter H. Aung, Myo Myint Toa, Pauline Ng, Shirelle Read, Eliot Tan, Wee Jin Brandtner, Eva Maria Dangerfield, John Salmons, Brian |
author_sort | Gunzburg, Walter H. |
collection | PubMed |
description | BACKGROUND: Gut microbiota in humans and animals play an important role in health, aiding in digestion, regulation of the immune system and protection against pathogens. Changes or imbalances in the gut microbiota (dysbiosis) have been linked to a variety of local and systemic diseases, and there is growing evidence that restoring the balance of the microbiota by delivery of probiotic microorganisms can improve health. However, orally delivered probiotic microorganisms must survive transit through lethal highly acid conditions of the stomach and bile salts in the small intestine. Current methods to protect probiotic microorganisms are still not effective enough. RESULTS: We have developed a cell encapsulation technology based on the natural polymer, cellulose sulphate (CS), that protects members of the microbiota from stomach acid and bile. Here we show that six commonly used probiotic strains (5 bacteria and 1 yeast) can be encapsulated within CS microspheres. These encapsulated strains survive low pH in vitro for at least 4 h without appreciable loss in viability as compared to their respective non-encapsulated counterparts. They also survive subsequent exposure to bile. The CS microspheres can be digested by cellulase at concentrations found in the human intestine, indicating one mechanism of release. Studies in mice that were fed CS encapsulated autofluorescing, commensal E. coli demonstrated release and colonization of the intestinal tract. CONCLUSION: Taken together, the data suggests that CS microencapsulation can protect bacteria and yeasts from viability losses due to stomach acid, allowing the use of lower oral doses of probiotics and microbiota, whilst ensuring good intestinal delivery and release. |
format | Online Article Text |
id | pubmed-7691082 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-76910822020-11-30 Efficient protection of microorganisms for delivery to the intestinal tract by cellulose sulphate encapsulation Gunzburg, Walter H. Aung, Myo Myint Toa, Pauline Ng, Shirelle Read, Eliot Tan, Wee Jin Brandtner, Eva Maria Dangerfield, John Salmons, Brian Microb Cell Fact Research BACKGROUND: Gut microbiota in humans and animals play an important role in health, aiding in digestion, regulation of the immune system and protection against pathogens. Changes or imbalances in the gut microbiota (dysbiosis) have been linked to a variety of local and systemic diseases, and there is growing evidence that restoring the balance of the microbiota by delivery of probiotic microorganisms can improve health. However, orally delivered probiotic microorganisms must survive transit through lethal highly acid conditions of the stomach and bile salts in the small intestine. Current methods to protect probiotic microorganisms are still not effective enough. RESULTS: We have developed a cell encapsulation technology based on the natural polymer, cellulose sulphate (CS), that protects members of the microbiota from stomach acid and bile. Here we show that six commonly used probiotic strains (5 bacteria and 1 yeast) can be encapsulated within CS microspheres. These encapsulated strains survive low pH in vitro for at least 4 h without appreciable loss in viability as compared to their respective non-encapsulated counterparts. They also survive subsequent exposure to bile. The CS microspheres can be digested by cellulase at concentrations found in the human intestine, indicating one mechanism of release. Studies in mice that were fed CS encapsulated autofluorescing, commensal E. coli demonstrated release and colonization of the intestinal tract. CONCLUSION: Taken together, the data suggests that CS microencapsulation can protect bacteria and yeasts from viability losses due to stomach acid, allowing the use of lower oral doses of probiotics and microbiota, whilst ensuring good intestinal delivery and release. BioMed Central 2020-11-26 /pmc/articles/PMC7691082/ /pubmed/33243224 http://dx.doi.org/10.1186/s12934-020-01465-3 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Gunzburg, Walter H. Aung, Myo Myint Toa, Pauline Ng, Shirelle Read, Eliot Tan, Wee Jin Brandtner, Eva Maria Dangerfield, John Salmons, Brian Efficient protection of microorganisms for delivery to the intestinal tract by cellulose sulphate encapsulation |
title | Efficient protection of microorganisms for delivery to the intestinal tract by cellulose sulphate encapsulation |
title_full | Efficient protection of microorganisms for delivery to the intestinal tract by cellulose sulphate encapsulation |
title_fullStr | Efficient protection of microorganisms for delivery to the intestinal tract by cellulose sulphate encapsulation |
title_full_unstemmed | Efficient protection of microorganisms for delivery to the intestinal tract by cellulose sulphate encapsulation |
title_short | Efficient protection of microorganisms for delivery to the intestinal tract by cellulose sulphate encapsulation |
title_sort | efficient protection of microorganisms for delivery to the intestinal tract by cellulose sulphate encapsulation |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7691082/ https://www.ncbi.nlm.nih.gov/pubmed/33243224 http://dx.doi.org/10.1186/s12934-020-01465-3 |
work_keys_str_mv | AT gunzburgwalterh efficientprotectionofmicroorganismsfordeliverytotheintestinaltractbycellulosesulphateencapsulation AT aungmyomyint efficientprotectionofmicroorganismsfordeliverytotheintestinaltractbycellulosesulphateencapsulation AT toapauline efficientprotectionofmicroorganismsfordeliverytotheintestinaltractbycellulosesulphateencapsulation AT ngshirelle efficientprotectionofmicroorganismsfordeliverytotheintestinaltractbycellulosesulphateencapsulation AT readeliot efficientprotectionofmicroorganismsfordeliverytotheintestinaltractbycellulosesulphateencapsulation AT tanweejin efficientprotectionofmicroorganismsfordeliverytotheintestinaltractbycellulosesulphateencapsulation AT brandtnerevamaria efficientprotectionofmicroorganismsfordeliverytotheintestinaltractbycellulosesulphateencapsulation AT dangerfieldjohn efficientprotectionofmicroorganismsfordeliverytotheintestinaltractbycellulosesulphateencapsulation AT salmonsbrian efficientprotectionofmicroorganismsfordeliverytotheintestinaltractbycellulosesulphateencapsulation |