Cargando…
Delivery Mode and Perinatal Antibiotics Influence the Infant Gut Bacteriome and Mycobiome: A Network Analysis
Both exposure to antibiotics at birth and delivery via Caesarean section influence the gut bacteriome’s development in infants. Using 16S rRNA and internal transcribed spacer sequencing on the Ion Torrent platform, we employed network analysis to investigate the bacterial and fungal interkingdom rel...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10381809/ https://www.ncbi.nlm.nih.gov/pubmed/37504707 http://dx.doi.org/10.3390/jof9070718 |
_version_ | 1785080535730618368 |
---|---|
author | Tejesvi, Mysore V. Turunen, Jenni Salmi, Sonja Reunanen, Justus Paalanne, Niko Tapiainen, Terhi |
author_facet | Tejesvi, Mysore V. Turunen, Jenni Salmi, Sonja Reunanen, Justus Paalanne, Niko Tapiainen, Terhi |
author_sort | Tejesvi, Mysore V. |
collection | PubMed |
description | Both exposure to antibiotics at birth and delivery via Caesarean section influence the gut bacteriome’s development in infants. Using 16S rRNA and internal transcribed spacer sequencing on the Ion Torrent platform, we employed network analysis to investigate the bacterial and fungal interkingdom relationships in the gut microbiome from birth to age 18 months in a prospective cohort study of 140 infants. The gut microbiome at ages six and 18 months revealed distinctive microbial interactions, including both positive and negative associations between bacterial and fungal genera in the gut ecosystem. Perinatal factors, delivery mode and intrapartum antibiotic exposure affected the associations between bacterial and fungal species. In infants exposed and unexposed to perinatal antibiotics, the gut microbiome formed distinct networks for the bacteriome and mycobiome. The fungi Saccharomyces, Trichosporon, Pezoloma, Cystofilobasidium, Rigidoporus and Fomitopsis were strongly associated with exposure to antibiotics at birth. Hyaloscypha, Trichosporon, Fomitopsis and Vishniacozyma were strongly associated with the control group that was not exposed to antibiotics. Five distinct networks were formed according to delivery mode. The present study confirms that bacteria and fungi clearly interact in the infant gut ecosystem. Furthermore, perinatal factors appear to influence the relationships between bacteria and fungi in the developing gut microbiome. |
format | Online Article Text |
id | pubmed-10381809 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-103818092023-07-29 Delivery Mode and Perinatal Antibiotics Influence the Infant Gut Bacteriome and Mycobiome: A Network Analysis Tejesvi, Mysore V. Turunen, Jenni Salmi, Sonja Reunanen, Justus Paalanne, Niko Tapiainen, Terhi J Fungi (Basel) Communication Both exposure to antibiotics at birth and delivery via Caesarean section influence the gut bacteriome’s development in infants. Using 16S rRNA and internal transcribed spacer sequencing on the Ion Torrent platform, we employed network analysis to investigate the bacterial and fungal interkingdom relationships in the gut microbiome from birth to age 18 months in a prospective cohort study of 140 infants. The gut microbiome at ages six and 18 months revealed distinctive microbial interactions, including both positive and negative associations between bacterial and fungal genera in the gut ecosystem. Perinatal factors, delivery mode and intrapartum antibiotic exposure affected the associations between bacterial and fungal species. In infants exposed and unexposed to perinatal antibiotics, the gut microbiome formed distinct networks for the bacteriome and mycobiome. The fungi Saccharomyces, Trichosporon, Pezoloma, Cystofilobasidium, Rigidoporus and Fomitopsis were strongly associated with exposure to antibiotics at birth. Hyaloscypha, Trichosporon, Fomitopsis and Vishniacozyma were strongly associated with the control group that was not exposed to antibiotics. Five distinct networks were formed according to delivery mode. The present study confirms that bacteria and fungi clearly interact in the infant gut ecosystem. Furthermore, perinatal factors appear to influence the relationships between bacteria and fungi in the developing gut microbiome. MDPI 2023-06-30 /pmc/articles/PMC10381809/ /pubmed/37504707 http://dx.doi.org/10.3390/jof9070718 Text en © 2023 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 | Communication Tejesvi, Mysore V. Turunen, Jenni Salmi, Sonja Reunanen, Justus Paalanne, Niko Tapiainen, Terhi Delivery Mode and Perinatal Antibiotics Influence the Infant Gut Bacteriome and Mycobiome: A Network Analysis |
title | Delivery Mode and Perinatal Antibiotics Influence the Infant Gut Bacteriome and Mycobiome: A Network Analysis |
title_full | Delivery Mode and Perinatal Antibiotics Influence the Infant Gut Bacteriome and Mycobiome: A Network Analysis |
title_fullStr | Delivery Mode and Perinatal Antibiotics Influence the Infant Gut Bacteriome and Mycobiome: A Network Analysis |
title_full_unstemmed | Delivery Mode and Perinatal Antibiotics Influence the Infant Gut Bacteriome and Mycobiome: A Network Analysis |
title_short | Delivery Mode and Perinatal Antibiotics Influence the Infant Gut Bacteriome and Mycobiome: A Network Analysis |
title_sort | delivery mode and perinatal antibiotics influence the infant gut bacteriome and mycobiome: a network analysis |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10381809/ https://www.ncbi.nlm.nih.gov/pubmed/37504707 http://dx.doi.org/10.3390/jof9070718 |
work_keys_str_mv | AT tejesvimysorev deliverymodeandperinatalantibioticsinfluencetheinfantgutbacteriomeandmycobiomeanetworkanalysis AT turunenjenni deliverymodeandperinatalantibioticsinfluencetheinfantgutbacteriomeandmycobiomeanetworkanalysis AT salmisonja deliverymodeandperinatalantibioticsinfluencetheinfantgutbacteriomeandmycobiomeanetworkanalysis AT reunanenjustus deliverymodeandperinatalantibioticsinfluencetheinfantgutbacteriomeandmycobiomeanetworkanalysis AT paalanneniko deliverymodeandperinatalantibioticsinfluencetheinfantgutbacteriomeandmycobiomeanetworkanalysis AT tapiainenterhi deliverymodeandperinatalantibioticsinfluencetheinfantgutbacteriomeandmycobiomeanetworkanalysis |