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Validation of a batch cultivation protocol for fecal microbiota of Kenyan infants

BACKGROUND: The combination of cultivation studies with molecular analysis approaches allows characterization of the complex human gut microbiota in depth. In vitro cultivation studies of infants living in rural sub-Saharan Africa are scarce. In this study, a batch cultivation protocol for Kenyan in...

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Autores principales: Rachmühl, Carole, Lacroix, Christophe, Giorgetti, Ambra, Stoffel, Nicole U., Zimmermann, Michael B., Brittenham, Gary M., Geirnaert, Annelies
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10318780/
https://www.ncbi.nlm.nih.gov/pubmed/37403024
http://dx.doi.org/10.1186/s12866-023-02915-9
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author Rachmühl, Carole
Lacroix, Christophe
Giorgetti, Ambra
Stoffel, Nicole U.
Zimmermann, Michael B.
Brittenham, Gary M.
Geirnaert, Annelies
author_facet Rachmühl, Carole
Lacroix, Christophe
Giorgetti, Ambra
Stoffel, Nicole U.
Zimmermann, Michael B.
Brittenham, Gary M.
Geirnaert, Annelies
author_sort Rachmühl, Carole
collection PubMed
description BACKGROUND: The combination of cultivation studies with molecular analysis approaches allows characterization of the complex human gut microbiota in depth. In vitro cultivation studies of infants living in rural sub-Saharan Africa are scarce. In this study, a batch cultivation protocol for Kenyan infant fecal microbiota was validated. METHODS: Fresh fecal samples were collected from 10 infants living in a rural area of Kenya. Samples were transported under protective conditions and subsequently prepared for inoculation within less than 30 h for batch cultivation. A diet-adapted cultivation medium was used that mimicked the daily intake of human milk and maize porridge in Kenyan infants during weaning. 16 S rRNA gene amplicon sequencing and HPLC analyses were performed to assess the composition and metabolic activity, respectively, of the fecal microbiota after 24 h of batch cultivation. RESULTS: High abundance of Bifidobacterium (53.4 ± 11.1%) and high proportions of acetate (56 ± 11% of total metabolites) and lactate (24 ± 22% of total metabolites) were detected in the Kenyan infant fecal microbiota. After cultivation started at an initial pH 7.6, the fraction of top bacterial genera (≥ 1% abundant) shared between fermentation and fecal samples was high at 97 ± 5%. However, Escherichia-Shigella, Clostridium sensu stricto 1, Bacteroides and Enterococcus were enriched concomitant with decreased Bifidobacterium abundance. Decreasing the initial pH to 6.9 lead to higher abundance of Bifidobacterium after incubation and increased the compositional similarity of fermentation and fecal samples. Despite similar total metabolite production of all fecal microbiota after cultivation, inter-individual differences in metabolite profiles were apparent. CONCLUSIONS: Protected transport and batch cultivation in host and diet adapted conditions allowed regrowth of the top abundant genera and reproduction of the metabolic activity of fresh Kenyan infant fecal microbiota. The validated batch cultivation protocol can be used to study the composition and functional potential of Kenyan infant fecal microbiota in vitro. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12866-023-02915-9.
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spelling pubmed-103187802023-07-05 Validation of a batch cultivation protocol for fecal microbiota of Kenyan infants Rachmühl, Carole Lacroix, Christophe Giorgetti, Ambra Stoffel, Nicole U. Zimmermann, Michael B. Brittenham, Gary M. Geirnaert, Annelies BMC Microbiol Research BACKGROUND: The combination of cultivation studies with molecular analysis approaches allows characterization of the complex human gut microbiota in depth. In vitro cultivation studies of infants living in rural sub-Saharan Africa are scarce. In this study, a batch cultivation protocol for Kenyan infant fecal microbiota was validated. METHODS: Fresh fecal samples were collected from 10 infants living in a rural area of Kenya. Samples were transported under protective conditions and subsequently prepared for inoculation within less than 30 h for batch cultivation. A diet-adapted cultivation medium was used that mimicked the daily intake of human milk and maize porridge in Kenyan infants during weaning. 16 S rRNA gene amplicon sequencing and HPLC analyses were performed to assess the composition and metabolic activity, respectively, of the fecal microbiota after 24 h of batch cultivation. RESULTS: High abundance of Bifidobacterium (53.4 ± 11.1%) and high proportions of acetate (56 ± 11% of total metabolites) and lactate (24 ± 22% of total metabolites) were detected in the Kenyan infant fecal microbiota. After cultivation started at an initial pH 7.6, the fraction of top bacterial genera (≥ 1% abundant) shared between fermentation and fecal samples was high at 97 ± 5%. However, Escherichia-Shigella, Clostridium sensu stricto 1, Bacteroides and Enterococcus were enriched concomitant with decreased Bifidobacterium abundance. Decreasing the initial pH to 6.9 lead to higher abundance of Bifidobacterium after incubation and increased the compositional similarity of fermentation and fecal samples. Despite similar total metabolite production of all fecal microbiota after cultivation, inter-individual differences in metabolite profiles were apparent. CONCLUSIONS: Protected transport and batch cultivation in host and diet adapted conditions allowed regrowth of the top abundant genera and reproduction of the metabolic activity of fresh Kenyan infant fecal microbiota. The validated batch cultivation protocol can be used to study the composition and functional potential of Kenyan infant fecal microbiota in vitro. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12866-023-02915-9. BioMed Central 2023-07-04 /pmc/articles/PMC10318780/ /pubmed/37403024 http://dx.doi.org/10.1186/s12866-023-02915-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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
Rachmühl, Carole
Lacroix, Christophe
Giorgetti, Ambra
Stoffel, Nicole U.
Zimmermann, Michael B.
Brittenham, Gary M.
Geirnaert, Annelies
Validation of a batch cultivation protocol for fecal microbiota of Kenyan infants
title Validation of a batch cultivation protocol for fecal microbiota of Kenyan infants
title_full Validation of a batch cultivation protocol for fecal microbiota of Kenyan infants
title_fullStr Validation of a batch cultivation protocol for fecal microbiota of Kenyan infants
title_full_unstemmed Validation of a batch cultivation protocol for fecal microbiota of Kenyan infants
title_short Validation of a batch cultivation protocol for fecal microbiota of Kenyan infants
title_sort validation of a batch cultivation protocol for fecal microbiota of kenyan infants
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10318780/
https://www.ncbi.nlm.nih.gov/pubmed/37403024
http://dx.doi.org/10.1186/s12866-023-02915-9
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