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Distinct mucosal microbial communities in infants with surgical necrotizing enterocolitis correlate with age and antibiotic exposure

OBJECTIVE: Necrotizing enterocolitis (NEC) is the most common surgical emergency in preterm infants, and pathogenesis associates with changes in the fecal microbiome. As fecal samples incompletely represent microbial communities in intestinal mucosa, we sought to determine the NEC tissue-specific mi...

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Autores principales: Romano-Keeler, Joann, Shilts, Meghan H., Tovchigrechko, Andrey, Wang, Chunlin, Brucker, Robert M., Moore, Daniel J., Fonnesbeck, Christopher, Meng, Shufang, Correa, Hernan, Lovvorn, Harold N., Tang, Yi-Wei, Hooper, Lora, Bordenstein, Seth R., Das, Suman R., Weitkamp, Jörn-Hendrik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6203398/
https://www.ncbi.nlm.nih.gov/pubmed/30365522
http://dx.doi.org/10.1371/journal.pone.0206366
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author Romano-Keeler, Joann
Shilts, Meghan H.
Tovchigrechko, Andrey
Wang, Chunlin
Brucker, Robert M.
Moore, Daniel J.
Fonnesbeck, Christopher
Meng, Shufang
Correa, Hernan
Lovvorn, Harold N.
Tang, Yi-Wei
Hooper, Lora
Bordenstein, Seth R.
Das, Suman R.
Weitkamp, Jörn-Hendrik
author_facet Romano-Keeler, Joann
Shilts, Meghan H.
Tovchigrechko, Andrey
Wang, Chunlin
Brucker, Robert M.
Moore, Daniel J.
Fonnesbeck, Christopher
Meng, Shufang
Correa, Hernan
Lovvorn, Harold N.
Tang, Yi-Wei
Hooper, Lora
Bordenstein, Seth R.
Das, Suman R.
Weitkamp, Jörn-Hendrik
author_sort Romano-Keeler, Joann
collection PubMed
description OBJECTIVE: Necrotizing enterocolitis (NEC) is the most common surgical emergency in preterm infants, and pathogenesis associates with changes in the fecal microbiome. As fecal samples incompletely represent microbial communities in intestinal mucosa, we sought to determine the NEC tissue-specific microbiome and assess its contribution to pathogenesis. DESIGN: We amplified and sequenced the V1-V3 hypervariable region of the bacterial 16S rRNA gene extracted from intestinal tissue and corresponding fecal samples from 12 surgical patients with NEC and 14 surgical patients without NEC. Low quality and non-bacterial sequences were removed, and taxonomic assignment was made with the Ribosomal Database Project. Operational taxonomic units were clustered at 97%. We tested for differences between NEC and non-NEC samples in microbiome alpha- and beta-diversity and differential abundance of specific taxa between NEC and non-NEC samples. Additional analyses were performed to assess the contribution of other demographic and environmental confounding factors on the infant tissue and fecal microbiome. RESULTS: The fecal and tissue microbial communities were different. NEC was associated with a distinct microbiome, which was characterized by low diversity, higher abundances of Staphylococcus and Clostridium_sensu_stricto, and lower abundances of Actinomyces and Corynebacterium. Infant age and vancomycin exposure correlated with shifts in the tissue microbiome. CONCLUSION: The observed low diversity in NEC tissues suggests that NEC is associated with a bacterial bloom and a distinct mucosal bacterial community. The exact bacterial species that constitute the bloom varied by infant and were strongly influenced by age and exposure to vancomycin.
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spelling pubmed-62033982018-11-19 Distinct mucosal microbial communities in infants with surgical necrotizing enterocolitis correlate with age and antibiotic exposure Romano-Keeler, Joann Shilts, Meghan H. Tovchigrechko, Andrey Wang, Chunlin Brucker, Robert M. Moore, Daniel J. Fonnesbeck, Christopher Meng, Shufang Correa, Hernan Lovvorn, Harold N. Tang, Yi-Wei Hooper, Lora Bordenstein, Seth R. Das, Suman R. Weitkamp, Jörn-Hendrik PLoS One Research Article OBJECTIVE: Necrotizing enterocolitis (NEC) is the most common surgical emergency in preterm infants, and pathogenesis associates with changes in the fecal microbiome. As fecal samples incompletely represent microbial communities in intestinal mucosa, we sought to determine the NEC tissue-specific microbiome and assess its contribution to pathogenesis. DESIGN: We amplified and sequenced the V1-V3 hypervariable region of the bacterial 16S rRNA gene extracted from intestinal tissue and corresponding fecal samples from 12 surgical patients with NEC and 14 surgical patients without NEC. Low quality and non-bacterial sequences were removed, and taxonomic assignment was made with the Ribosomal Database Project. Operational taxonomic units were clustered at 97%. We tested for differences between NEC and non-NEC samples in microbiome alpha- and beta-diversity and differential abundance of specific taxa between NEC and non-NEC samples. Additional analyses were performed to assess the contribution of other demographic and environmental confounding factors on the infant tissue and fecal microbiome. RESULTS: The fecal and tissue microbial communities were different. NEC was associated with a distinct microbiome, which was characterized by low diversity, higher abundances of Staphylococcus and Clostridium_sensu_stricto, and lower abundances of Actinomyces and Corynebacterium. Infant age and vancomycin exposure correlated with shifts in the tissue microbiome. CONCLUSION: The observed low diversity in NEC tissues suggests that NEC is associated with a bacterial bloom and a distinct mucosal bacterial community. The exact bacterial species that constitute the bloom varied by infant and were strongly influenced by age and exposure to vancomycin. Public Library of Science 2018-10-26 /pmc/articles/PMC6203398/ /pubmed/30365522 http://dx.doi.org/10.1371/journal.pone.0206366 Text en © 2018 Romano-Keeler 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Romano-Keeler, Joann
Shilts, Meghan H.
Tovchigrechko, Andrey
Wang, Chunlin
Brucker, Robert M.
Moore, Daniel J.
Fonnesbeck, Christopher
Meng, Shufang
Correa, Hernan
Lovvorn, Harold N.
Tang, Yi-Wei
Hooper, Lora
Bordenstein, Seth R.
Das, Suman R.
Weitkamp, Jörn-Hendrik
Distinct mucosal microbial communities in infants with surgical necrotizing enterocolitis correlate with age and antibiotic exposure
title Distinct mucosal microbial communities in infants with surgical necrotizing enterocolitis correlate with age and antibiotic exposure
title_full Distinct mucosal microbial communities in infants with surgical necrotizing enterocolitis correlate with age and antibiotic exposure
title_fullStr Distinct mucosal microbial communities in infants with surgical necrotizing enterocolitis correlate with age and antibiotic exposure
title_full_unstemmed Distinct mucosal microbial communities in infants with surgical necrotizing enterocolitis correlate with age and antibiotic exposure
title_short Distinct mucosal microbial communities in infants with surgical necrotizing enterocolitis correlate with age and antibiotic exposure
title_sort distinct mucosal microbial communities in infants with surgical necrotizing enterocolitis correlate with age and antibiotic exposure
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6203398/
https://www.ncbi.nlm.nih.gov/pubmed/30365522
http://dx.doi.org/10.1371/journal.pone.0206366
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