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Bifidobacterium longum Subspecies infantis Strain EVC001 Decreases Neonatal Murine Necrotizing Enterocolitis

Necrotizing enterocolitis (NEC) is a disease mainly of preterm infants with a 30–50% mortality rate and long-term morbidities for survivors. Treatment strategies are limited and have not improved in decades, prompting research into prevention strategies, particularly with probiotics. Recent work wit...

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Autores principales: Lueschow, Shiloh R., Boly, Timothy J., Frese, Steven A., Casaburi, Giorgio, Mitchell, Ryan D., Henrick, Bethany M., McElroy, Steven J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8839161/
https://www.ncbi.nlm.nih.gov/pubmed/35276854
http://dx.doi.org/10.3390/nu14030495
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author Lueschow, Shiloh R.
Boly, Timothy J.
Frese, Steven A.
Casaburi, Giorgio
Mitchell, Ryan D.
Henrick, Bethany M.
McElroy, Steven J.
author_facet Lueschow, Shiloh R.
Boly, Timothy J.
Frese, Steven A.
Casaburi, Giorgio
Mitchell, Ryan D.
Henrick, Bethany M.
McElroy, Steven J.
author_sort Lueschow, Shiloh R.
collection PubMed
description Necrotizing enterocolitis (NEC) is a disease mainly of preterm infants with a 30–50% mortality rate and long-term morbidities for survivors. Treatment strategies are limited and have not improved in decades, prompting research into prevention strategies, particularly with probiotics. Recent work with the probiotic B. infantis EVC001 suggests that this organism may generate a more appropriate microbiome for preterm infants who generally have inappropriate gut colonization and inflammation, both risk factors for NEC. Experimental NEC involving Paneth cell disruption in combination with bacterial dysbiosis or formula feeding was induced in P14-16 C57Bl/6 mice with or without gavaged B. infantis. Following completion of the model, serum, small intestinal tissue, the cecum, and colon were harvested to examine inflammatory cytokines, injury, and the microbiome, respectively. EVC001 treatment significantly decreased NEC in a bacterial dysbiosis dependent model, but this decrease was model-dependent. In the NEC model dependent on formula feeding, no difference in injury was observed, but trending to significant differences was observed in serum cytokines. EVC001 also improved wound closure at six and twelve hours compared to the sham control in intestinal epithelial monolayers. These findings suggest that B. infantis EVC001 can prevent experimental NEC through anti-inflammatory and epithelial barrier restoration properties.
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spelling pubmed-88391612022-02-13 Bifidobacterium longum Subspecies infantis Strain EVC001 Decreases Neonatal Murine Necrotizing Enterocolitis Lueschow, Shiloh R. Boly, Timothy J. Frese, Steven A. Casaburi, Giorgio Mitchell, Ryan D. Henrick, Bethany M. McElroy, Steven J. Nutrients Article Necrotizing enterocolitis (NEC) is a disease mainly of preterm infants with a 30–50% mortality rate and long-term morbidities for survivors. Treatment strategies are limited and have not improved in decades, prompting research into prevention strategies, particularly with probiotics. Recent work with the probiotic B. infantis EVC001 suggests that this organism may generate a more appropriate microbiome for preterm infants who generally have inappropriate gut colonization and inflammation, both risk factors for NEC. Experimental NEC involving Paneth cell disruption in combination with bacterial dysbiosis or formula feeding was induced in P14-16 C57Bl/6 mice with or without gavaged B. infantis. Following completion of the model, serum, small intestinal tissue, the cecum, and colon were harvested to examine inflammatory cytokines, injury, and the microbiome, respectively. EVC001 treatment significantly decreased NEC in a bacterial dysbiosis dependent model, but this decrease was model-dependent. In the NEC model dependent on formula feeding, no difference in injury was observed, but trending to significant differences was observed in serum cytokines. EVC001 also improved wound closure at six and twelve hours compared to the sham control in intestinal epithelial monolayers. These findings suggest that B. infantis EVC001 can prevent experimental NEC through anti-inflammatory and epithelial barrier restoration properties. MDPI 2022-01-24 /pmc/articles/PMC8839161/ /pubmed/35276854 http://dx.doi.org/10.3390/nu14030495 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lueschow, Shiloh R.
Boly, Timothy J.
Frese, Steven A.
Casaburi, Giorgio
Mitchell, Ryan D.
Henrick, Bethany M.
McElroy, Steven J.
Bifidobacterium longum Subspecies infantis Strain EVC001 Decreases Neonatal Murine Necrotizing Enterocolitis
title Bifidobacterium longum Subspecies infantis Strain EVC001 Decreases Neonatal Murine Necrotizing Enterocolitis
title_full Bifidobacterium longum Subspecies infantis Strain EVC001 Decreases Neonatal Murine Necrotizing Enterocolitis
title_fullStr Bifidobacterium longum Subspecies infantis Strain EVC001 Decreases Neonatal Murine Necrotizing Enterocolitis
title_full_unstemmed Bifidobacterium longum Subspecies infantis Strain EVC001 Decreases Neonatal Murine Necrotizing Enterocolitis
title_short Bifidobacterium longum Subspecies infantis Strain EVC001 Decreases Neonatal Murine Necrotizing Enterocolitis
title_sort bifidobacterium longum subspecies infantis strain evc001 decreases neonatal murine necrotizing enterocolitis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8839161/
https://www.ncbi.nlm.nih.gov/pubmed/35276854
http://dx.doi.org/10.3390/nu14030495
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