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Maternal amoxicillin affects piglets colon microbiota: microbial ecology and metabolomics in a gut model

ABSTRACT: The first weeks of life represent a crucial stage for microbial colonization of the piglets’ gastrointestinal tract. Newborns’ microbiota is unstable and easily subject to changes under stimuli or insults. Nonetheless, the administration of antibiotics to the sow is still considered as com...

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Autores principales: Nissen, Lorenzo, Aniballi, Camilla, Casciano, Flavia, Elmi, Alberto, Ventrella, Domenico, Zannoni, Augusta, Gianotti, Andrea, Bacci, Maria Laura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9666337/
https://www.ncbi.nlm.nih.gov/pubmed/36239764
http://dx.doi.org/10.1007/s00253-022-12223-3
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author Nissen, Lorenzo
Aniballi, Camilla
Casciano, Flavia
Elmi, Alberto
Ventrella, Domenico
Zannoni, Augusta
Gianotti, Andrea
Bacci, Maria Laura
author_facet Nissen, Lorenzo
Aniballi, Camilla
Casciano, Flavia
Elmi, Alberto
Ventrella, Domenico
Zannoni, Augusta
Gianotti, Andrea
Bacci, Maria Laura
author_sort Nissen, Lorenzo
collection PubMed
description ABSTRACT: The first weeks of life represent a crucial stage for microbial colonization of the piglets’ gastrointestinal tract. Newborns’ microbiota is unstable and easily subject to changes under stimuli or insults. Nonetheless, the administration of antibiotics to the sow is still considered as common practice in intensive farming for pathological conditions in the postpartum. Therefore, transfer of antibiotic residues through milk may occurs, affecting the piglets’ colon microbiota. In this study, we aimed to extend the knowledge on antibiotic transfer through milk, employing an in vitro dedicated piglet colon model (MICODE—Multi Unit In vitro Colon Model). The authors’ focus was set on the shifts of the piglets’ microbiota composition microbiomics (16S r-DNA MiSeq and qPCR—quantitative polymerase chain reaction) and on the production of microbial metabolites (SPME GC/MS—solid phase micro-extraction gas chromatography/mass spectrometry) in response to milk with different concentrations of amoxicillin. The results showed an effective influence of amoxicillin in piglets’ microbiota and metabolites production; however, without altering the overall biodiversity. The scenario is that of a limitation of pathogens and opportunistic taxa, e.g., Staphylococcaceae and Enterobacteriaceae, but also a limitation of commensal dominant Lactobacillaceae, a reduction in commensal Ruminococcaceae and a depletion in beneficial Bifidobactericeae. Lastly, an incremental growth of resistant species, such as Enterococcaceae or Clostridiaceae, was observed. To the authors’ knowledge, this study is the first evaluating the impact of antibiotic residues towards the piglets’ colon microbiota in an in vitro model, opening the way to include such approach in a pipeline of experiments where a reduced number of animals for testing is employed. KEY POINTS: • Piglet colon model to study antibiotic transfer through milk. • MICODE resulted a robust and versatile in vitro gut model. • Towards the “3Rs” Principles to replace, reduce and refine the use of animals used for scientific purposes (Directive 2010/63/UE). GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00253-022-12223-3.
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spelling pubmed-96663372022-11-17 Maternal amoxicillin affects piglets colon microbiota: microbial ecology and metabolomics in a gut model Nissen, Lorenzo Aniballi, Camilla Casciano, Flavia Elmi, Alberto Ventrella, Domenico Zannoni, Augusta Gianotti, Andrea Bacci, Maria Laura Appl Microbiol Biotechnol Applied Microbial and Cell Physiology ABSTRACT: The first weeks of life represent a crucial stage for microbial colonization of the piglets’ gastrointestinal tract. Newborns’ microbiota is unstable and easily subject to changes under stimuli or insults. Nonetheless, the administration of antibiotics to the sow is still considered as common practice in intensive farming for pathological conditions in the postpartum. Therefore, transfer of antibiotic residues through milk may occurs, affecting the piglets’ colon microbiota. In this study, we aimed to extend the knowledge on antibiotic transfer through milk, employing an in vitro dedicated piglet colon model (MICODE—Multi Unit In vitro Colon Model). The authors’ focus was set on the shifts of the piglets’ microbiota composition microbiomics (16S r-DNA MiSeq and qPCR—quantitative polymerase chain reaction) and on the production of microbial metabolites (SPME GC/MS—solid phase micro-extraction gas chromatography/mass spectrometry) in response to milk with different concentrations of amoxicillin. The results showed an effective influence of amoxicillin in piglets’ microbiota and metabolites production; however, without altering the overall biodiversity. The scenario is that of a limitation of pathogens and opportunistic taxa, e.g., Staphylococcaceae and Enterobacteriaceae, but also a limitation of commensal dominant Lactobacillaceae, a reduction in commensal Ruminococcaceae and a depletion in beneficial Bifidobactericeae. Lastly, an incremental growth of resistant species, such as Enterococcaceae or Clostridiaceae, was observed. To the authors’ knowledge, this study is the first evaluating the impact of antibiotic residues towards the piglets’ colon microbiota in an in vitro model, opening the way to include such approach in a pipeline of experiments where a reduced number of animals for testing is employed. KEY POINTS: • Piglet colon model to study antibiotic transfer through milk. • MICODE resulted a robust and versatile in vitro gut model. • Towards the “3Rs” Principles to replace, reduce and refine the use of animals used for scientific purposes (Directive 2010/63/UE). GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00253-022-12223-3. Springer Berlin Heidelberg 2022-10-14 2022 /pmc/articles/PMC9666337/ /pubmed/36239764 http://dx.doi.org/10.1007/s00253-022-12223-3 Text en © The Author(s) 2022 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/) .
spellingShingle Applied Microbial and Cell Physiology
Nissen, Lorenzo
Aniballi, Camilla
Casciano, Flavia
Elmi, Alberto
Ventrella, Domenico
Zannoni, Augusta
Gianotti, Andrea
Bacci, Maria Laura
Maternal amoxicillin affects piglets colon microbiota: microbial ecology and metabolomics in a gut model
title Maternal amoxicillin affects piglets colon microbiota: microbial ecology and metabolomics in a gut model
title_full Maternal amoxicillin affects piglets colon microbiota: microbial ecology and metabolomics in a gut model
title_fullStr Maternal amoxicillin affects piglets colon microbiota: microbial ecology and metabolomics in a gut model
title_full_unstemmed Maternal amoxicillin affects piglets colon microbiota: microbial ecology and metabolomics in a gut model
title_short Maternal amoxicillin affects piglets colon microbiota: microbial ecology and metabolomics in a gut model
title_sort maternal amoxicillin affects piglets colon microbiota: microbial ecology and metabolomics in a gut model
topic Applied Microbial and Cell Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9666337/
https://www.ncbi.nlm.nih.gov/pubmed/36239764
http://dx.doi.org/10.1007/s00253-022-12223-3
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