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Lactobacillaceae and Cell Adhesion: Genomic and Functional Screening

The analysis of collections of lactic acid bacteria (LAB) from traditional fermented plant foods in tropical countries may enable the detection of LAB with interesting properties. Binding capacity is often the main criterion used to investigate the probiotic characteristics of bacteria. In this stud...

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Autores principales: Turpin, Williams, Humblot, Christèle, Noordine, Marie-Louise, Thomas, Muriel, Guyot, Jean-Pierre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3364998/
https://www.ncbi.nlm.nih.gov/pubmed/22675431
http://dx.doi.org/10.1371/journal.pone.0038034
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author Turpin, Williams
Humblot, Christèle
Noordine, Marie-Louise
Thomas, Muriel
Guyot, Jean-Pierre
author_facet Turpin, Williams
Humblot, Christèle
Noordine, Marie-Louise
Thomas, Muriel
Guyot, Jean-Pierre
author_sort Turpin, Williams
collection PubMed
description The analysis of collections of lactic acid bacteria (LAB) from traditional fermented plant foods in tropical countries may enable the detection of LAB with interesting properties. Binding capacity is often the main criterion used to investigate the probiotic characteristics of bacteria. In this study, we focused on a collection of 163 Lactobacillaceace comprising 156 bacteria isolated from traditional amylaceous fermented foods and seven strains taken from a collection and used as controls. The collection had a series of analyses to assess binding potential for the selection of new probiotic candidates. The presence/absence of 14 genes involved in binding to the gastrointestinal tract was assessed. This enabled the detection of all the housekeeping genes (ef-Tu, eno, gap, groEl and srtA) in the entire collection, of some of the other genes (apf, cnb, fpbA, mapA, mub) in 86% to 100% of LAB, and of the other genes (cbsA, gtf, msa, slpA) in 0% to 8% of LAB. Most of the bacteria isolated from traditional fermented foods exhibited a genetic profile favorable for their binding to the gastrointestinal tract. We selected 30 strains with different genetic profiles to test their binding ability to non-mucus (HT29) and mucus secreting (HT29-MTX) cell lines as well as their ability to degrade mucus. Assays on both lines revealed high variability in binding properties among the LAB, depending on the cell model used. Finally, we investigated if their binding ability was linked to tighter cross-talk between bacteria and eukaryotic cells by measuring the expression of bacterial genes and of the eukaryotic MUC2 gene. Results showed that wild LAB from tropical amylaceous fermented food had a much higher binding capacity than the two LAB currently known to be probiotics. However their adhesion was not linked to any particular genetic equipment.
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spelling pubmed-33649982012-06-06 Lactobacillaceae and Cell Adhesion: Genomic and Functional Screening Turpin, Williams Humblot, Christèle Noordine, Marie-Louise Thomas, Muriel Guyot, Jean-Pierre PLoS One Research Article The analysis of collections of lactic acid bacteria (LAB) from traditional fermented plant foods in tropical countries may enable the detection of LAB with interesting properties. Binding capacity is often the main criterion used to investigate the probiotic characteristics of bacteria. In this study, we focused on a collection of 163 Lactobacillaceace comprising 156 bacteria isolated from traditional amylaceous fermented foods and seven strains taken from a collection and used as controls. The collection had a series of analyses to assess binding potential for the selection of new probiotic candidates. The presence/absence of 14 genes involved in binding to the gastrointestinal tract was assessed. This enabled the detection of all the housekeeping genes (ef-Tu, eno, gap, groEl and srtA) in the entire collection, of some of the other genes (apf, cnb, fpbA, mapA, mub) in 86% to 100% of LAB, and of the other genes (cbsA, gtf, msa, slpA) in 0% to 8% of LAB. Most of the bacteria isolated from traditional fermented foods exhibited a genetic profile favorable for their binding to the gastrointestinal tract. We selected 30 strains with different genetic profiles to test their binding ability to non-mucus (HT29) and mucus secreting (HT29-MTX) cell lines as well as their ability to degrade mucus. Assays on both lines revealed high variability in binding properties among the LAB, depending on the cell model used. Finally, we investigated if their binding ability was linked to tighter cross-talk between bacteria and eukaryotic cells by measuring the expression of bacterial genes and of the eukaryotic MUC2 gene. Results showed that wild LAB from tropical amylaceous fermented food had a much higher binding capacity than the two LAB currently known to be probiotics. However their adhesion was not linked to any particular genetic equipment. Public Library of Science 2012-05-31 /pmc/articles/PMC3364998/ /pubmed/22675431 http://dx.doi.org/10.1371/journal.pone.0038034 Text en Turpin et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Turpin, Williams
Humblot, Christèle
Noordine, Marie-Louise
Thomas, Muriel
Guyot, Jean-Pierre
Lactobacillaceae and Cell Adhesion: Genomic and Functional Screening
title Lactobacillaceae and Cell Adhesion: Genomic and Functional Screening
title_full Lactobacillaceae and Cell Adhesion: Genomic and Functional Screening
title_fullStr Lactobacillaceae and Cell Adhesion: Genomic and Functional Screening
title_full_unstemmed Lactobacillaceae and Cell Adhesion: Genomic and Functional Screening
title_short Lactobacillaceae and Cell Adhesion: Genomic and Functional Screening
title_sort lactobacillaceae and cell adhesion: genomic and functional screening
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3364998/
https://www.ncbi.nlm.nih.gov/pubmed/22675431
http://dx.doi.org/10.1371/journal.pone.0038034
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