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Encapsulation of E. coli phage ZCEC5 in chitosan–alginate beads as a delivery system in phage therapy

Bacteriophages can be used successfully to treat pathogenic bacteria in the food chain including zoonotic pathogens that colonize the intestines of farm animals. However, harsh gastric conditions of low pH and digestive enzyme activities affect phage viability, and accordingly reduce their effective...

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Autores principales: Abdelsattar, Abdallah S., Abdelrahman, Fatma, Dawoud, Alyaa, Connerton, Ian F., El-Shibiny, Ayman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6579803/
https://www.ncbi.nlm.nih.gov/pubmed/31209685
http://dx.doi.org/10.1186/s13568-019-0810-9
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author Abdelsattar, Abdallah S.
Abdelrahman, Fatma
Dawoud, Alyaa
Connerton, Ian F.
El-Shibiny, Ayman
author_facet Abdelsattar, Abdallah S.
Abdelrahman, Fatma
Dawoud, Alyaa
Connerton, Ian F.
El-Shibiny, Ayman
author_sort Abdelsattar, Abdallah S.
collection PubMed
description Bacteriophages can be used successfully to treat pathogenic bacteria in the food chain including zoonotic pathogens that colonize the intestines of farm animals. However, harsh gastric conditions of low pH and digestive enzyme activities affect phage viability, and accordingly reduce their effectiveness. We report the development of a natural protective barrier suitable for oral administration to farm animals that confers acid stability before functional release of bead-encapsulated phages. Escherichia coli bacteriophage ZSEC5 is rendered inactive at pH 2.0 but encapsulation in chitosan–alginate bead with a honey and gelatin matrix limited titer reductions to 1 log(10) PFU mL(−1). The encapsulated phage titers were stable upon storage in water but achieved near complete release over 4–5 h in a simulated intestinal solution (0.1% bile salt, 0.4% pancreatin, 50 mM KH(2)PO(4) pH 7.5) at 37 °C. Exposure of E. coli O157:H7 to the bead-encapsulated phage preparations produced a delayed response, reaching a maximal reductions of 4.2 to 4.8 log(10) CFU mL(−1) after 10 h at 37 °C under simulated intestinal conditions compared to a maximal reduction of 5.1 log(10) CFU mL(−1) at 3 h for free phage applied at MOI = 1. Bead-encapsulation is a promising reliable and cost-effective method for the functional delivery of bacteriophage targeting intestinal bacteria of farm animals.
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spelling pubmed-65798032019-07-05 Encapsulation of E. coli phage ZCEC5 in chitosan–alginate beads as a delivery system in phage therapy Abdelsattar, Abdallah S. Abdelrahman, Fatma Dawoud, Alyaa Connerton, Ian F. El-Shibiny, Ayman AMB Express Original Article Bacteriophages can be used successfully to treat pathogenic bacteria in the food chain including zoonotic pathogens that colonize the intestines of farm animals. However, harsh gastric conditions of low pH and digestive enzyme activities affect phage viability, and accordingly reduce their effectiveness. We report the development of a natural protective barrier suitable for oral administration to farm animals that confers acid stability before functional release of bead-encapsulated phages. Escherichia coli bacteriophage ZSEC5 is rendered inactive at pH 2.0 but encapsulation in chitosan–alginate bead with a honey and gelatin matrix limited titer reductions to 1 log(10) PFU mL(−1). The encapsulated phage titers were stable upon storage in water but achieved near complete release over 4–5 h in a simulated intestinal solution (0.1% bile salt, 0.4% pancreatin, 50 mM KH(2)PO(4) pH 7.5) at 37 °C. Exposure of E. coli O157:H7 to the bead-encapsulated phage preparations produced a delayed response, reaching a maximal reductions of 4.2 to 4.8 log(10) CFU mL(−1) after 10 h at 37 °C under simulated intestinal conditions compared to a maximal reduction of 5.1 log(10) CFU mL(−1) at 3 h for free phage applied at MOI = 1. Bead-encapsulation is a promising reliable and cost-effective method for the functional delivery of bacteriophage targeting intestinal bacteria of farm animals. Springer Berlin Heidelberg 2019-06-17 /pmc/articles/PMC6579803/ /pubmed/31209685 http://dx.doi.org/10.1186/s13568-019-0810-9 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
Abdelsattar, Abdallah S.
Abdelrahman, Fatma
Dawoud, Alyaa
Connerton, Ian F.
El-Shibiny, Ayman
Encapsulation of E. coli phage ZCEC5 in chitosan–alginate beads as a delivery system in phage therapy
title Encapsulation of E. coli phage ZCEC5 in chitosan–alginate beads as a delivery system in phage therapy
title_full Encapsulation of E. coli phage ZCEC5 in chitosan–alginate beads as a delivery system in phage therapy
title_fullStr Encapsulation of E. coli phage ZCEC5 in chitosan–alginate beads as a delivery system in phage therapy
title_full_unstemmed Encapsulation of E. coli phage ZCEC5 in chitosan–alginate beads as a delivery system in phage therapy
title_short Encapsulation of E. coli phage ZCEC5 in chitosan–alginate beads as a delivery system in phage therapy
title_sort encapsulation of e. coli phage zcec5 in chitosan–alginate beads as a delivery system in phage therapy
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6579803/
https://www.ncbi.nlm.nih.gov/pubmed/31209685
http://dx.doi.org/10.1186/s13568-019-0810-9
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