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Proof of Concept of Culturomics Use of Time of Care
Culturomics, a high throughput culture method with rapid identification of the colonies by Matrix Assisted Laser Desorption Ionization/Time Of Flight Mass Spectrometry (MALDI-TOF MS), has demonstrated its contribution to the exploration of the gut microbiota over the past 10 years. However, the cost...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7719802/ https://www.ncbi.nlm.nih.gov/pubmed/33330116 http://dx.doi.org/10.3389/fcimb.2020.524769 |
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author | Naud, Sabrina Khelaifia, Saber Mbogning Fonkou, Maxime Descartes Dione, Niokhor Lagier, Jean-Christophe Raoult, Didier |
author_facet | Naud, Sabrina Khelaifia, Saber Mbogning Fonkou, Maxime Descartes Dione, Niokhor Lagier, Jean-Christophe Raoult, Didier |
author_sort | Naud, Sabrina |
collection | PubMed |
description | Culturomics, a high throughput culture method with rapid identification of the colonies by Matrix Assisted Laser Desorption Ionization/Time Of Flight Mass Spectrometry (MALDI-TOF MS), has demonstrated its contribution to the exploration of the gut microbiota over the past 10 years. However, the cost, work time and workload, considerably limit its use on a large scale or emergency context. Here, by testing two different stool samples, including a stool sample from a patient requiring rapid immunotherapy treatment, we tested a new fast culturomic protocol using two pre-incubation media, blood culture bottle and YCFA modified medium. Both media were supplemented with 2 ml of rumen fluid filtered at 0.2 μm and 2 ml of defibrinated and sterile sheep blood. Unlike the standard culturomics, subculturing of blood culture bottle were performed at reduced incubation time (3 h, 6 h, 9 h, 24 h) and at a longer incubation time (3 days, 7 days, and 10 days) at 37°C. By testing 5,200 colonies per MALDI-TOF MS and obtaining a comparable number of cultured bacterial species (131 to 143) in a stool sample, this new protocol reduced the number of colonies tested by 57%, working time by 78.6% and cost by 72.2%. In addition, we highlighted that the proportion of strict anaerobic species has increased by 24%, known to be the preferential targets for biotherapy, including Faecalibacterium prausnitzii, Akkermansia muciniphila, Christensenella minuta, and Phascolarctobacterium faecium. Finally, this work showed that some bacterial species grew earlier but disappeared with prolonged incubation times. |
format | Online Article Text |
id | pubmed-7719802 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77198022020-12-15 Proof of Concept of Culturomics Use of Time of Care Naud, Sabrina Khelaifia, Saber Mbogning Fonkou, Maxime Descartes Dione, Niokhor Lagier, Jean-Christophe Raoult, Didier Front Cell Infect Microbiol Cellular and Infection Microbiology Culturomics, a high throughput culture method with rapid identification of the colonies by Matrix Assisted Laser Desorption Ionization/Time Of Flight Mass Spectrometry (MALDI-TOF MS), has demonstrated its contribution to the exploration of the gut microbiota over the past 10 years. However, the cost, work time and workload, considerably limit its use on a large scale or emergency context. Here, by testing two different stool samples, including a stool sample from a patient requiring rapid immunotherapy treatment, we tested a new fast culturomic protocol using two pre-incubation media, blood culture bottle and YCFA modified medium. Both media were supplemented with 2 ml of rumen fluid filtered at 0.2 μm and 2 ml of defibrinated and sterile sheep blood. Unlike the standard culturomics, subculturing of blood culture bottle were performed at reduced incubation time (3 h, 6 h, 9 h, 24 h) and at a longer incubation time (3 days, 7 days, and 10 days) at 37°C. By testing 5,200 colonies per MALDI-TOF MS and obtaining a comparable number of cultured bacterial species (131 to 143) in a stool sample, this new protocol reduced the number of colonies tested by 57%, working time by 78.6% and cost by 72.2%. In addition, we highlighted that the proportion of strict anaerobic species has increased by 24%, known to be the preferential targets for biotherapy, including Faecalibacterium prausnitzii, Akkermansia muciniphila, Christensenella minuta, and Phascolarctobacterium faecium. Finally, this work showed that some bacterial species grew earlier but disappeared with prolonged incubation times. Frontiers Media S.A. 2020-11-23 /pmc/articles/PMC7719802/ /pubmed/33330116 http://dx.doi.org/10.3389/fcimb.2020.524769 Text en Copyright © 2020 Naud, Khelaifia, Mbogning Fonkou, Dione, Lagier and Raoult http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cellular and Infection Microbiology Naud, Sabrina Khelaifia, Saber Mbogning Fonkou, Maxime Descartes Dione, Niokhor Lagier, Jean-Christophe Raoult, Didier Proof of Concept of Culturomics Use of Time of Care |
title | Proof of Concept of Culturomics Use of Time of Care |
title_full | Proof of Concept of Culturomics Use of Time of Care |
title_fullStr | Proof of Concept of Culturomics Use of Time of Care |
title_full_unstemmed | Proof of Concept of Culturomics Use of Time of Care |
title_short | Proof of Concept of Culturomics Use of Time of Care |
title_sort | proof of concept of culturomics use of time of care |
topic | Cellular and Infection Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7719802/ https://www.ncbi.nlm.nih.gov/pubmed/33330116 http://dx.doi.org/10.3389/fcimb.2020.524769 |
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