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Bacteria and Bioactivity in Holder Pasteurized and Shelf-Stable Human Milk Products

Background: Historically, Holder pasteurization has been used to pasteurize donor human milk available in a hospital setting. There is extensive research that provides an overview of the impact of Holder pasteurization on bioactive components of human milk. A shelf-stable (SS) human milk product, cr...

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Autores principales: Lima, Hope K, Wagner-Gillespie, Montana, Perrin, Maryanne T, Fogleman, April D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5998364/
https://www.ncbi.nlm.nih.gov/pubmed/29955718
http://dx.doi.org/10.3945/cdn.117.001438
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author Lima, Hope K
Wagner-Gillespie, Montana
Perrin, Maryanne T
Fogleman, April D
author_facet Lima, Hope K
Wagner-Gillespie, Montana
Perrin, Maryanne T
Fogleman, April D
author_sort Lima, Hope K
collection PubMed
description Background: Historically, Holder pasteurization has been used to pasteurize donor human milk available in a hospital setting. There is extensive research that provides an overview of the impact of Holder pasteurization on bioactive components of human milk. A shelf-stable (SS) human milk product, created using retort processing, recently became available; however, to our knowledge, little has been published about the effect of retort processing on human milk. Objective: We aimed to assess the ability of retort processing to eliminate bacteria and to quantify the difference in lysozyme and secretory immunoglobulin A (sIgA) activity between Holder pasteurized (HP) and SS human milk. Methods: Milk samples from 60 mothers were pooled. From this pool, 36 samples were taken: 12 samples were kept raw, 12 samples were HP, and 12 samples were retort processed to create an SS product. All samples were analyzed for total aerobic bacteria, coliform bacteria, Bacillus cereus, sIgA activity, and lysozyme activity. Raw samples served as the control. Results: One raw sample and 3 HP samples contained B. cereus at the time of culture. There were no detectable bacteria in SS samples at the time of culture. Raw samples had significantly greater lysozyme and sIgA activity than HP and SS samples (P < 0.0001). HP samples retained significantly more lysozyme and sIgA activity (54% and 87%, respectively) than SS samples (0% and 11%, respectively). Conclusions: Human milk processed using Holder pasteurization should continue to be screened for the presence of B. cereus. Clinicians should be aware of the differences in the retention of lysozyme and sIgA activity in HP and SS products when making feeding decisions for medically fragile or immunocompromised infants to ensure that patients are receiving the maximum immune protection.
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spelling pubmed-59983642018-06-28 Bacteria and Bioactivity in Holder Pasteurized and Shelf-Stable Human Milk Products Lima, Hope K Wagner-Gillespie, Montana Perrin, Maryanne T Fogleman, April D Curr Dev Nutr Original Research Background: Historically, Holder pasteurization has been used to pasteurize donor human milk available in a hospital setting. There is extensive research that provides an overview of the impact of Holder pasteurization on bioactive components of human milk. A shelf-stable (SS) human milk product, created using retort processing, recently became available; however, to our knowledge, little has been published about the effect of retort processing on human milk. Objective: We aimed to assess the ability of retort processing to eliminate bacteria and to quantify the difference in lysozyme and secretory immunoglobulin A (sIgA) activity between Holder pasteurized (HP) and SS human milk. Methods: Milk samples from 60 mothers were pooled. From this pool, 36 samples were taken: 12 samples were kept raw, 12 samples were HP, and 12 samples were retort processed to create an SS product. All samples were analyzed for total aerobic bacteria, coliform bacteria, Bacillus cereus, sIgA activity, and lysozyme activity. Raw samples served as the control. Results: One raw sample and 3 HP samples contained B. cereus at the time of culture. There were no detectable bacteria in SS samples at the time of culture. Raw samples had significantly greater lysozyme and sIgA activity than HP and SS samples (P < 0.0001). HP samples retained significantly more lysozyme and sIgA activity (54% and 87%, respectively) than SS samples (0% and 11%, respectively). Conclusions: Human milk processed using Holder pasteurization should continue to be screened for the presence of B. cereus. Clinicians should be aware of the differences in the retention of lysozyme and sIgA activity in HP and SS products when making feeding decisions for medically fragile or immunocompromised infants to ensure that patients are receiving the maximum immune protection. Oxford University Press 2017-08-02 /pmc/articles/PMC5998364/ /pubmed/29955718 http://dx.doi.org/10.3945/cdn.117.001438 Text en Copyright © 2017, Lima et al. http://creativecommons.org/licenses/by-nc/4.0/ This is an open access article distributed under the terms of the CCBY-NC License http://creativecommons.org/licenses/by-nc/4.0/, which permits noncommercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Lima, Hope K
Wagner-Gillespie, Montana
Perrin, Maryanne T
Fogleman, April D
Bacteria and Bioactivity in Holder Pasteurized and Shelf-Stable Human Milk Products
title Bacteria and Bioactivity in Holder Pasteurized and Shelf-Stable Human Milk Products
title_full Bacteria and Bioactivity in Holder Pasteurized and Shelf-Stable Human Milk Products
title_fullStr Bacteria and Bioactivity in Holder Pasteurized and Shelf-Stable Human Milk Products
title_full_unstemmed Bacteria and Bioactivity in Holder Pasteurized and Shelf-Stable Human Milk Products
title_short Bacteria and Bioactivity in Holder Pasteurized and Shelf-Stable Human Milk Products
title_sort bacteria and bioactivity in holder pasteurized and shelf-stable human milk products
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5998364/
https://www.ncbi.nlm.nih.gov/pubmed/29955718
http://dx.doi.org/10.3945/cdn.117.001438
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