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Intravenous antibiotics in preterm infants have a negative effect upon microbiome development throughout preterm life
BACKGROUND: Intestinal dysbiosis is implicated in the origins of necrotising enterocolitis and late-onset sepsis in preterm babies. However, the effect of modulators of bacterial growth (e.g. antibiotics) upon the developing microbiome is not well-characterised. In this prospectively-recruited, retr...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10120188/ https://www.ncbi.nlm.nih.gov/pubmed/37085896 http://dx.doi.org/10.1186/s13099-023-00544-1 |
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author | Hutchinson, R. A. Costeloe, K. L. Wade, W. G. Millar, M. R. Ansbro, K. Stacey, F. Fleming, P. F. |
author_facet | Hutchinson, R. A. Costeloe, K. L. Wade, W. G. Millar, M. R. Ansbro, K. Stacey, F. Fleming, P. F. |
author_sort | Hutchinson, R. A. |
collection | PubMed |
description | BACKGROUND: Intestinal dysbiosis is implicated in the origins of necrotising enterocolitis and late-onset sepsis in preterm babies. However, the effect of modulators of bacterial growth (e.g. antibiotics) upon the developing microbiome is not well-characterised. In this prospectively-recruited, retrospectively-classified, case–control study, high-throughput 16S rRNA gene sequencing was combined with contemporaneous clinical data collection, to assess the within-subject relationship between antibiotic administration and microbiome development, in comparison to preterm infants with minimal antibiotic exposure. RESULTS: During courses of antibiotics, diversity progression fell in comparison to that seen outside periods of antibiotic use (-0.71units/week vs. + 0.63units/week, p < 0.01); Enterobacteriaceae relative abundance progression conversely rose (+ 10.6%/week vs. -8.9%/week, p < 0.01). After antibiotic cessation, diversity progression remained suppressed (+ 0.2units/week, p = 0.02). CONCLUSIONS: Antibiotic use has an acute and longer-lasting impact on the developing preterm intestinal microbiome. This has clinical implications with regard to the contribution of antibiotic use to evolving dysbiosis, and affects the interpretation of existing microbiome studies where this effect modulator is rarely accounted for. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13099-023-00544-1. |
format | Online Article Text |
id | pubmed-10120188 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-101201882023-04-22 Intravenous antibiotics in preterm infants have a negative effect upon microbiome development throughout preterm life Hutchinson, R. A. Costeloe, K. L. Wade, W. G. Millar, M. R. Ansbro, K. Stacey, F. Fleming, P. F. Gut Pathog Research BACKGROUND: Intestinal dysbiosis is implicated in the origins of necrotising enterocolitis and late-onset sepsis in preterm babies. However, the effect of modulators of bacterial growth (e.g. antibiotics) upon the developing microbiome is not well-characterised. In this prospectively-recruited, retrospectively-classified, case–control study, high-throughput 16S rRNA gene sequencing was combined with contemporaneous clinical data collection, to assess the within-subject relationship between antibiotic administration and microbiome development, in comparison to preterm infants with minimal antibiotic exposure. RESULTS: During courses of antibiotics, diversity progression fell in comparison to that seen outside periods of antibiotic use (-0.71units/week vs. + 0.63units/week, p < 0.01); Enterobacteriaceae relative abundance progression conversely rose (+ 10.6%/week vs. -8.9%/week, p < 0.01). After antibiotic cessation, diversity progression remained suppressed (+ 0.2units/week, p = 0.02). CONCLUSIONS: Antibiotic use has an acute and longer-lasting impact on the developing preterm intestinal microbiome. This has clinical implications with regard to the contribution of antibiotic use to evolving dysbiosis, and affects the interpretation of existing microbiome studies where this effect modulator is rarely accounted for. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13099-023-00544-1. BioMed Central 2023-04-21 /pmc/articles/PMC10120188/ /pubmed/37085896 http://dx.doi.org/10.1186/s13099-023-00544-1 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Hutchinson, R. A. Costeloe, K. L. Wade, W. G. Millar, M. R. Ansbro, K. Stacey, F. Fleming, P. F. Intravenous antibiotics in preterm infants have a negative effect upon microbiome development throughout preterm life |
title | Intravenous antibiotics in preterm infants have a negative effect upon microbiome development throughout preterm life |
title_full | Intravenous antibiotics in preterm infants have a negative effect upon microbiome development throughout preterm life |
title_fullStr | Intravenous antibiotics in preterm infants have a negative effect upon microbiome development throughout preterm life |
title_full_unstemmed | Intravenous antibiotics in preterm infants have a negative effect upon microbiome development throughout preterm life |
title_short | Intravenous antibiotics in preterm infants have a negative effect upon microbiome development throughout preterm life |
title_sort | intravenous antibiotics in preterm infants have a negative effect upon microbiome development throughout preterm life |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10120188/ https://www.ncbi.nlm.nih.gov/pubmed/37085896 http://dx.doi.org/10.1186/s13099-023-00544-1 |
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