Efficacy of Different Encapsulation Techniques on the Viability and Stability of Diverse Phage under Simulated Gastric Conditions

<i>Salmonella</i> causes a range of diseases in humans and livestock of considerable public health and economic importance. Widespread antimicrobial use, particularly in intensively produced livestock (e.g., poultry and pigs) may contribute to the rise of multidrug-resistant <i>Sal...

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Main Authors: Sicelo B. Dlamini, Adriano M. Gigante, Steven P. T. Hooton, Robert J. Atterbury
Format: Article
Language:English
Published: MDPI AG 2023-09-01
Series:Microorganisms
Subjects:
Online Access:https://www.mdpi.com/2076-2607/11/10/2389
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author Sicelo B. Dlamini
Adriano M. Gigante
Steven P. T. Hooton
Robert J. Atterbury
author_facet Sicelo B. Dlamini
Adriano M. Gigante
Steven P. T. Hooton
Robert J. Atterbury
author_sort Sicelo B. Dlamini
collection DOAJ
description <i>Salmonella</i> causes a range of diseases in humans and livestock of considerable public health and economic importance. Widespread antimicrobial use, particularly in intensively produced livestock (e.g., poultry and pigs) may contribute to the rise of multidrug-resistant <i>Salmonella</i> strains. Alternative treatments such as bacteriophages have shown promise when used to reduce the intestinal carriage of <i>Salmonella</i> in livestock. However, the digestive enzymes and low pH encountered in the monogastric GI tract can significantly reduce phage viability and impact therapeutic outcomes. This study deployed alginate–carrageenan microcapsules with and without CaCO<sub>3</sub> to protect a genomically diverse set of five <i>Salmonella</i> bacteriophages from simulated gastrointestinal conditions. None of the unprotected phage could be recovered following exposure to pH < 3 for 10 min. Alginate–carrageenan encapsulation improved phage viability at pH 2–2.5 after exposure for 10 min, but not at pH 2 after 1 h. Including 1% (<i>w</i>/<i>v</i>) CaCO<sub>3</sub> in the formulation further reduced phage loss to <0.5 log<sub>10</sub> PFU/mL, even after 1 h at pH 2. In all cases, phage were efficiently released from the microcapsules following a shift to a neutral pH (7.5), simulating passage to the duodenum. In summary, alginate–carrageenan-CaCO<sub>3</sub> encapsulation is a promising approach for targeted intestinal delivery of genomically diverse <i>Salmonella</i> bacteriophages.
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spelling doaj.art-682d7d8454954aa1830d59b64bdcca0a2023-11-19T17:25:58ZengMDPI AGMicroorganisms2076-26072023-09-011110238910.3390/microorganisms11102389Efficacy of Different Encapsulation Techniques on the Viability and Stability of Diverse Phage under Simulated Gastric ConditionsSicelo B. Dlamini0Adriano M. Gigante1Steven P. T. Hooton2Robert J. Atterbury3School of Agricultural Sciences, Faculty of Agriculture and Natural Sciences, University of Mpumalanga, Nelspruit 1200, South AfricaSchool of Veterinary Medicine and Science, University of Nottingham, Sutton Bonington, Leicestershire LE12 5RD, UKDepartment of Genetics and Genome Biology, University of Leicester, University Road, Leicester LE1 7RH, UKSchool of Veterinary Medicine and Science, University of Nottingham, Sutton Bonington, Leicestershire LE12 5RD, UK<i>Salmonella</i> causes a range of diseases in humans and livestock of considerable public health and economic importance. Widespread antimicrobial use, particularly in intensively produced livestock (e.g., poultry and pigs) may contribute to the rise of multidrug-resistant <i>Salmonella</i> strains. Alternative treatments such as bacteriophages have shown promise when used to reduce the intestinal carriage of <i>Salmonella</i> in livestock. However, the digestive enzymes and low pH encountered in the monogastric GI tract can significantly reduce phage viability and impact therapeutic outcomes. This study deployed alginate–carrageenan microcapsules with and without CaCO<sub>3</sub> to protect a genomically diverse set of five <i>Salmonella</i> bacteriophages from simulated gastrointestinal conditions. None of the unprotected phage could be recovered following exposure to pH < 3 for 10 min. Alginate–carrageenan encapsulation improved phage viability at pH 2–2.5 after exposure for 10 min, but not at pH 2 after 1 h. Including 1% (<i>w</i>/<i>v</i>) CaCO<sub>3</sub> in the formulation further reduced phage loss to <0.5 log<sub>10</sub> PFU/mL, even after 1 h at pH 2. In all cases, phage were efficiently released from the microcapsules following a shift to a neutral pH (7.5), simulating passage to the duodenum. In summary, alginate–carrageenan-CaCO<sub>3</sub> encapsulation is a promising approach for targeted intestinal delivery of genomically diverse <i>Salmonella</i> bacteriophages.https://www.mdpi.com/2076-2607/11/10/2389bacteriophageencapsulationpoultrypigmonogastricfeed
spellingShingle Sicelo B. Dlamini
Adriano M. Gigante
Steven P. T. Hooton
Robert J. Atterbury
Efficacy of Different Encapsulation Techniques on the Viability and Stability of Diverse Phage under Simulated Gastric Conditions
Microorganisms
bacteriophage
encapsulation
poultry
pig
monogastric
feed
title Efficacy of Different Encapsulation Techniques on the Viability and Stability of Diverse Phage under Simulated Gastric Conditions
title_full Efficacy of Different Encapsulation Techniques on the Viability and Stability of Diverse Phage under Simulated Gastric Conditions
title_fullStr Efficacy of Different Encapsulation Techniques on the Viability and Stability of Diverse Phage under Simulated Gastric Conditions
title_full_unstemmed Efficacy of Different Encapsulation Techniques on the Viability and Stability of Diverse Phage under Simulated Gastric Conditions
title_short Efficacy of Different Encapsulation Techniques on the Viability and Stability of Diverse Phage under Simulated Gastric Conditions
title_sort efficacy of different encapsulation techniques on the viability and stability of diverse phage under simulated gastric conditions
topic bacteriophage
encapsulation
poultry
pig
monogastric
feed
url https://www.mdpi.com/2076-2607/11/10/2389
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AT stevenpthooton efficacyofdifferentencapsulationtechniquesontheviabilityandstabilityofdiversephageundersimulatedgastricconditions
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