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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2012
Materias:
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.
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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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