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Bifidobacterium bifidum in a Rat Model of Necrotizing Enterocolitis: Antimicrobial Peptide and Protein Responses
Necrotizing enterocolitis (NEC) is a devastating disease of premature infants. Probiotics decrease the risk of NEC in clinical and experimental studies. Antimicrobial peptides protect the gut against noxious microbes and shape the commensal microbiota, but their role in NEC remains unclear. We repor...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3619207/ https://www.ncbi.nlm.nih.gov/pubmed/22322385 http://dx.doi.org/10.1038/pr.2012.11 |
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author | Underwood, Mark A. Kananurak, Anchasa Coursodon, Christine F. Adkins-Reick, Camille K. Chu, Hiutung Bennett, Stephen H. Wehkamp, Jan Castillo, Patricia A. Leonard, Brian C. Tancredi, Daniel J. Sherman, Michael P. Dvorak, Bohuslav Bevins, Charles L. |
author_facet | Underwood, Mark A. Kananurak, Anchasa Coursodon, Christine F. Adkins-Reick, Camille K. Chu, Hiutung Bennett, Stephen H. Wehkamp, Jan Castillo, Patricia A. Leonard, Brian C. Tancredi, Daniel J. Sherman, Michael P. Dvorak, Bohuslav Bevins, Charles L. |
author_sort | Underwood, Mark A. |
collection | PubMed |
description | Necrotizing enterocolitis (NEC) is a devastating disease of premature infants. Probiotics decrease the risk of NEC in clinical and experimental studies. Antimicrobial peptides protect the gut against noxious microbes and shape the commensal microbiota, but their role in NEC remains unclear. We report that like in human ontogeny, the rat pup has low expression of Paneth cell antimicrobials, which increases rapidly during normal development. To investigate the expression of antimicrobial peptides in experimental NEC and the impact of probiotics on their expression, premature rats were divided into three groups: dam fed (DF), hand fed with formula (FF), or hand fed with formula containing Bifidobacterium bifidum (FF+BIF). All groups were exposed to asphyxia and cold stress. The expression of lysozyme, secretory phospholipase A(2), pancreatic-associated proteins 1 and 3 mRNA was elevated in the FF (NEC) group, compared to the DF and FF+BIF groups where disease was attenuated. We conclude that induction of antimicrobial peptides occurs in experimental NEC similar to that reported in human disease and is attenuated when disease is averted by probiotic B. bifidum. The induction of antimicrobial peptides is likely an adaptive mucosal response that is often not sufficient to prevent disease in the premature gut. |
format | Online Article Text |
id | pubmed-3619207 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
record_format | MEDLINE/PubMed |
spelling | pubmed-36192072013-04-08 Bifidobacterium bifidum in a Rat Model of Necrotizing Enterocolitis: Antimicrobial Peptide and Protein Responses Underwood, Mark A. Kananurak, Anchasa Coursodon, Christine F. Adkins-Reick, Camille K. Chu, Hiutung Bennett, Stephen H. Wehkamp, Jan Castillo, Patricia A. Leonard, Brian C. Tancredi, Daniel J. Sherman, Michael P. Dvorak, Bohuslav Bevins, Charles L. Pediatr Res Article Necrotizing enterocolitis (NEC) is a devastating disease of premature infants. Probiotics decrease the risk of NEC in clinical and experimental studies. Antimicrobial peptides protect the gut against noxious microbes and shape the commensal microbiota, but their role in NEC remains unclear. We report that like in human ontogeny, the rat pup has low expression of Paneth cell antimicrobials, which increases rapidly during normal development. To investigate the expression of antimicrobial peptides in experimental NEC and the impact of probiotics on their expression, premature rats were divided into three groups: dam fed (DF), hand fed with formula (FF), or hand fed with formula containing Bifidobacterium bifidum (FF+BIF). All groups were exposed to asphyxia and cold stress. The expression of lysozyme, secretory phospholipase A(2), pancreatic-associated proteins 1 and 3 mRNA was elevated in the FF (NEC) group, compared to the DF and FF+BIF groups where disease was attenuated. We conclude that induction of antimicrobial peptides occurs in experimental NEC similar to that reported in human disease and is attenuated when disease is averted by probiotic B. bifidum. The induction of antimicrobial peptides is likely an adaptive mucosal response that is often not sufficient to prevent disease in the premature gut. 2012-02-09 2012-05 /pmc/articles/PMC3619207/ /pubmed/22322385 http://dx.doi.org/10.1038/pr.2012.11 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Underwood, Mark A. Kananurak, Anchasa Coursodon, Christine F. Adkins-Reick, Camille K. Chu, Hiutung Bennett, Stephen H. Wehkamp, Jan Castillo, Patricia A. Leonard, Brian C. Tancredi, Daniel J. Sherman, Michael P. Dvorak, Bohuslav Bevins, Charles L. Bifidobacterium bifidum in a Rat Model of Necrotizing Enterocolitis: Antimicrobial Peptide and Protein Responses |
title | Bifidobacterium bifidum in a Rat Model of Necrotizing Enterocolitis: Antimicrobial Peptide and Protein Responses |
title_full | Bifidobacterium bifidum in a Rat Model of Necrotizing Enterocolitis: Antimicrobial Peptide and Protein Responses |
title_fullStr | Bifidobacterium bifidum in a Rat Model of Necrotizing Enterocolitis: Antimicrobial Peptide and Protein Responses |
title_full_unstemmed | Bifidobacterium bifidum in a Rat Model of Necrotizing Enterocolitis: Antimicrobial Peptide and Protein Responses |
title_short | Bifidobacterium bifidum in a Rat Model of Necrotizing Enterocolitis: Antimicrobial Peptide and Protein Responses |
title_sort | bifidobacterium bifidum in a rat model of necrotizing enterocolitis: antimicrobial peptide and protein responses |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3619207/ https://www.ncbi.nlm.nih.gov/pubmed/22322385 http://dx.doi.org/10.1038/pr.2012.11 |
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