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Fecal Microbiota in Premature Infants Prior to Necrotizing Enterocolitis

Intestinal luminal microbiota likely contribute to the etiology of necrotizing enterocolitis (NEC), a common disease in preterm infants. Microbiota development, a cascade of initial colonization events leading to the establishment of a diverse commensal microbiota, can now be studied in preterm infa...

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Autores principales: Mai, Volker, Young, Christopher Michael, Ukhanova, Maria, Wang, Xiaoyu, Sun, Yijun, Casella, George, Theriaque, Douglas, Li, Nan, Sharma, Renu, Hudak, Mark, Neu, Josef
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3108958/
https://www.ncbi.nlm.nih.gov/pubmed/21674011
http://dx.doi.org/10.1371/journal.pone.0020647
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author Mai, Volker
Young, Christopher Michael
Ukhanova, Maria
Wang, Xiaoyu
Sun, Yijun
Casella, George
Theriaque, Douglas
Li, Nan
Sharma, Renu
Hudak, Mark
Neu, Josef
author_facet Mai, Volker
Young, Christopher Michael
Ukhanova, Maria
Wang, Xiaoyu
Sun, Yijun
Casella, George
Theriaque, Douglas
Li, Nan
Sharma, Renu
Hudak, Mark
Neu, Josef
author_sort Mai, Volker
collection PubMed
description Intestinal luminal microbiota likely contribute to the etiology of necrotizing enterocolitis (NEC), a common disease in preterm infants. Microbiota development, a cascade of initial colonization events leading to the establishment of a diverse commensal microbiota, can now be studied in preterm infants using powerful molecular tools. Starting with the first stool and continuing until discharge, weekly stool specimens were collected prospectively from infants with gestational ages ≤32 completed weeks or birth weights≤1250 g. High throughput 16S rRNA sequencing was used to compare the diversity of microbiota and the prevalence of specific bacterial signatures in nine NEC infants and in nine matched controls. After removal of short and low quality reads we retained a total of 110,021 sequences. Microbiota composition differed in the matched samples collected 1 week but not <72 hours prior to NEC diagnosis. We detected a bloom (34% increase) of Proteobacteria and a decrease (32%) in Firmicutes in NEC cases between the 1 week and <72 hour samples. No significant change was identified in the controls. At both time points, molecular signatures were identified that were increased in NEC cases. One of the bacterial signatures detected more frequently in NEC cases (p<0.01) matched closest to γ-Proteobacteria. Although this sequence grouped to the well-studied Enterobacteriaceae family, it did not match any sequence in Genbank by more than 97%. Our observations suggest that abnormal patterns of microbiota and potentially a novel pathogen contribute to the etiology of NEC.
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spelling pubmed-31089582011-06-13 Fecal Microbiota in Premature Infants Prior to Necrotizing Enterocolitis Mai, Volker Young, Christopher Michael Ukhanova, Maria Wang, Xiaoyu Sun, Yijun Casella, George Theriaque, Douglas Li, Nan Sharma, Renu Hudak, Mark Neu, Josef PLoS One Research Article Intestinal luminal microbiota likely contribute to the etiology of necrotizing enterocolitis (NEC), a common disease in preterm infants. Microbiota development, a cascade of initial colonization events leading to the establishment of a diverse commensal microbiota, can now be studied in preterm infants using powerful molecular tools. Starting with the first stool and continuing until discharge, weekly stool specimens were collected prospectively from infants with gestational ages ≤32 completed weeks or birth weights≤1250 g. High throughput 16S rRNA sequencing was used to compare the diversity of microbiota and the prevalence of specific bacterial signatures in nine NEC infants and in nine matched controls. After removal of short and low quality reads we retained a total of 110,021 sequences. Microbiota composition differed in the matched samples collected 1 week but not <72 hours prior to NEC diagnosis. We detected a bloom (34% increase) of Proteobacteria and a decrease (32%) in Firmicutes in NEC cases between the 1 week and <72 hour samples. No significant change was identified in the controls. At both time points, molecular signatures were identified that were increased in NEC cases. One of the bacterial signatures detected more frequently in NEC cases (p<0.01) matched closest to γ-Proteobacteria. Although this sequence grouped to the well-studied Enterobacteriaceae family, it did not match any sequence in Genbank by more than 97%. Our observations suggest that abnormal patterns of microbiota and potentially a novel pathogen contribute to the etiology of NEC. Public Library of Science 2011-06-06 /pmc/articles/PMC3108958/ /pubmed/21674011 http://dx.doi.org/10.1371/journal.pone.0020647 Text en Mai et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Mai, Volker
Young, Christopher Michael
Ukhanova, Maria
Wang, Xiaoyu
Sun, Yijun
Casella, George
Theriaque, Douglas
Li, Nan
Sharma, Renu
Hudak, Mark
Neu, Josef
Fecal Microbiota in Premature Infants Prior to Necrotizing Enterocolitis
title Fecal Microbiota in Premature Infants Prior to Necrotizing Enterocolitis
title_full Fecal Microbiota in Premature Infants Prior to Necrotizing Enterocolitis
title_fullStr Fecal Microbiota in Premature Infants Prior to Necrotizing Enterocolitis
title_full_unstemmed Fecal Microbiota in Premature Infants Prior to Necrotizing Enterocolitis
title_short Fecal Microbiota in Premature Infants Prior to Necrotizing Enterocolitis
title_sort fecal microbiota in premature infants prior to necrotizing enterocolitis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3108958/
https://www.ncbi.nlm.nih.gov/pubmed/21674011
http://dx.doi.org/10.1371/journal.pone.0020647
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