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Enriched bovine IgG fraction prevents infections with Enterohaemorrhagic Escherichia coli O157:H7, Salmonella enterica serovar Enteritidis, and Mycobacterium avium
A bovine IgG‐enriched whey fraction contains antibodies against various bacterial antigens. We investigated the protective effects of a bovine whey fraction preparation against infections with Enterohaemorrhagic Escherichia coli O157:H7, Salmonella enterica serovar Enteritidis, and Mycobacterium avi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6694433/ https://www.ncbi.nlm.nih.gov/pubmed/31428360 http://dx.doi.org/10.1002/fsn3.1134 |
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author | Funatogawa, Keiji Tada, Tatsuya Kuwahara‐Arai, Kyoko Kirikae, Teruo Takahashi, Masao |
author_facet | Funatogawa, Keiji Tada, Tatsuya Kuwahara‐Arai, Kyoko Kirikae, Teruo Takahashi, Masao |
author_sort | Funatogawa, Keiji |
collection | PubMed |
description | A bovine IgG‐enriched whey fraction contains antibodies against various bacterial antigens. We investigated the protective effects of a bovine whey fraction preparation against infections with Enterohaemorrhagic Escherichia coli O157:H7, Salmonella enterica serovar Enteritidis, and Mycobacterium avium in mouse models. After infection with these pathogens, the IgG‐enriched fraction or skim milk was given ad libitum at a 5% solution instead of water. The mice given the IgG‐enriched fraction were significantly resistant to orally challenged EHEC O157:H7 (LD(50): 4.0 × 10(5) CFU/mouse) infections compared with the mice given skim milk (LD(50): <1.5 × 10(2) CFU/mouse). The mice given the IgG‐enriched fraction were also significantly resistant to orally challenged S. Enteritidis (LD(50): 5.0 × 10(6) CFU/mouse) infections compared with the mice given skim milk (LD(50): <2.5 × 10(1) CFU/mouse). When the mice were nasally infected with M. avium, the numbers of the bacteria in lungs of mice given the IgG‐enriched fraction were significantly lower than those given skim milk 2 and 3 weeks after infection. These results strongly indicate that oral administration of the bovine IgG‐enriched whey fraction protects mice against food‐borne infection and also that it partially protects mice against respiratory tract infection. |
format | Online Article Text |
id | pubmed-6694433 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-66944332019-08-19 Enriched bovine IgG fraction prevents infections with Enterohaemorrhagic Escherichia coli O157:H7, Salmonella enterica serovar Enteritidis, and Mycobacterium avium Funatogawa, Keiji Tada, Tatsuya Kuwahara‐Arai, Kyoko Kirikae, Teruo Takahashi, Masao Food Sci Nutr Original Research A bovine IgG‐enriched whey fraction contains antibodies against various bacterial antigens. We investigated the protective effects of a bovine whey fraction preparation against infections with Enterohaemorrhagic Escherichia coli O157:H7, Salmonella enterica serovar Enteritidis, and Mycobacterium avium in mouse models. After infection with these pathogens, the IgG‐enriched fraction or skim milk was given ad libitum at a 5% solution instead of water. The mice given the IgG‐enriched fraction were significantly resistant to orally challenged EHEC O157:H7 (LD(50): 4.0 × 10(5) CFU/mouse) infections compared with the mice given skim milk (LD(50): <1.5 × 10(2) CFU/mouse). The mice given the IgG‐enriched fraction were also significantly resistant to orally challenged S. Enteritidis (LD(50): 5.0 × 10(6) CFU/mouse) infections compared with the mice given skim milk (LD(50): <2.5 × 10(1) CFU/mouse). When the mice were nasally infected with M. avium, the numbers of the bacteria in lungs of mice given the IgG‐enriched fraction were significantly lower than those given skim milk 2 and 3 weeks after infection. These results strongly indicate that oral administration of the bovine IgG‐enriched whey fraction protects mice against food‐borne infection and also that it partially protects mice against respiratory tract infection. John Wiley and Sons Inc. 2019-07-17 /pmc/articles/PMC6694433/ /pubmed/31428360 http://dx.doi.org/10.1002/fsn3.1134 Text en © 2019 The Authors. Food Science & Nutrition published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Funatogawa, Keiji Tada, Tatsuya Kuwahara‐Arai, Kyoko Kirikae, Teruo Takahashi, Masao Enriched bovine IgG fraction prevents infections with Enterohaemorrhagic Escherichia coli O157:H7, Salmonella enterica serovar Enteritidis, and Mycobacterium avium |
title | Enriched bovine IgG fraction prevents infections with Enterohaemorrhagic Escherichia coli O157:H7, Salmonella enterica serovar Enteritidis, and Mycobacterium avium
|
title_full | Enriched bovine IgG fraction prevents infections with Enterohaemorrhagic Escherichia coli O157:H7, Salmonella enterica serovar Enteritidis, and Mycobacterium avium
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title_fullStr | Enriched bovine IgG fraction prevents infections with Enterohaemorrhagic Escherichia coli O157:H7, Salmonella enterica serovar Enteritidis, and Mycobacterium avium
|
title_full_unstemmed | Enriched bovine IgG fraction prevents infections with Enterohaemorrhagic Escherichia coli O157:H7, Salmonella enterica serovar Enteritidis, and Mycobacterium avium
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title_short | Enriched bovine IgG fraction prevents infections with Enterohaemorrhagic Escherichia coli O157:H7, Salmonella enterica serovar Enteritidis, and Mycobacterium avium
|
title_sort | enriched bovine igg fraction prevents infections with enterohaemorrhagic escherichia coli o157:h7, salmonella enterica serovar enteritidis, and mycobacterium avium |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6694433/ https://www.ncbi.nlm.nih.gov/pubmed/31428360 http://dx.doi.org/10.1002/fsn3.1134 |
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