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Analysis of a phase-variable restriction modification system of the human gut symbiont Bacteroides fragilis

The genomes of gut Bacteroidales contain numerous invertible regions, many of which contain promoters that dictate phase-variable synthesis of surface molecules such as polysaccharides, fimbriae, and outer surface proteins. Here, we characterize a different type of phase-variable system of Bacteroid...

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Autores principales: Ben-Assa, Nadav, Coyne, Michael J, Fomenkov, Alexey, Livny, Jonathan, Robins, William P, Muniesa, Maite, Carey, Vincent, Carasso, Shaqed, Gefen, Tal, Jofre, Juan, Roberts, Richard J, Comstock, Laurie E, Geva-Zatorsky, Naama
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7641763/
https://www.ncbi.nlm.nih.gov/pubmed/33045731
http://dx.doi.org/10.1093/nar/gkaa824
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author Ben-Assa, Nadav
Coyne, Michael J
Fomenkov, Alexey
Livny, Jonathan
Robins, William P
Muniesa, Maite
Carey, Vincent
Carasso, Shaqed
Gefen, Tal
Jofre, Juan
Roberts, Richard J
Comstock, Laurie E
Geva-Zatorsky, Naama
author_facet Ben-Assa, Nadav
Coyne, Michael J
Fomenkov, Alexey
Livny, Jonathan
Robins, William P
Muniesa, Maite
Carey, Vincent
Carasso, Shaqed
Gefen, Tal
Jofre, Juan
Roberts, Richard J
Comstock, Laurie E
Geva-Zatorsky, Naama
author_sort Ben-Assa, Nadav
collection PubMed
description The genomes of gut Bacteroidales contain numerous invertible regions, many of which contain promoters that dictate phase-variable synthesis of surface molecules such as polysaccharides, fimbriae, and outer surface proteins. Here, we characterize a different type of phase-variable system of Bacteroides fragilis, a Type I restriction modification system (R-M). We show that reversible DNA inversions within this R-M locus leads to the generation of eight specificity proteins with distinct recognition sites. In vitro grown bacteria have a different proportion of specificity gene combinations at the expression locus than bacteria isolated from the mammalian gut. By creating mutants, each able to produce only one specificity protein from this region, we identified the R-M recognition sites of four of these S-proteins using SMRT sequencing. Transcriptome analysis revealed that the locked specificity mutants, whether grown in vitro or isolated from the mammalian gut, have distinct transcriptional profiles, likely creating different phenotypes, one of which was confirmed. Genomic analyses of diverse strains of Bacteroidetes from both host-associated and environmental sources reveal the ubiquity of phase-variable R-M systems in this phylum.
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spelling pubmed-76417632020-11-10 Analysis of a phase-variable restriction modification system of the human gut symbiont Bacteroides fragilis Ben-Assa, Nadav Coyne, Michael J Fomenkov, Alexey Livny, Jonathan Robins, William P Muniesa, Maite Carey, Vincent Carasso, Shaqed Gefen, Tal Jofre, Juan Roberts, Richard J Comstock, Laurie E Geva-Zatorsky, Naama Nucleic Acids Res Molecular Biology The genomes of gut Bacteroidales contain numerous invertible regions, many of which contain promoters that dictate phase-variable synthesis of surface molecules such as polysaccharides, fimbriae, and outer surface proteins. Here, we characterize a different type of phase-variable system of Bacteroides fragilis, a Type I restriction modification system (R-M). We show that reversible DNA inversions within this R-M locus leads to the generation of eight specificity proteins with distinct recognition sites. In vitro grown bacteria have a different proportion of specificity gene combinations at the expression locus than bacteria isolated from the mammalian gut. By creating mutants, each able to produce only one specificity protein from this region, we identified the R-M recognition sites of four of these S-proteins using SMRT sequencing. Transcriptome analysis revealed that the locked specificity mutants, whether grown in vitro or isolated from the mammalian gut, have distinct transcriptional profiles, likely creating different phenotypes, one of which was confirmed. Genomic analyses of diverse strains of Bacteroidetes from both host-associated and environmental sources reveal the ubiquity of phase-variable R-M systems in this phylum. Oxford University Press 2020-10-12 /pmc/articles/PMC7641763/ /pubmed/33045731 http://dx.doi.org/10.1093/nar/gkaa824 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Molecular Biology
Ben-Assa, Nadav
Coyne, Michael J
Fomenkov, Alexey
Livny, Jonathan
Robins, William P
Muniesa, Maite
Carey, Vincent
Carasso, Shaqed
Gefen, Tal
Jofre, Juan
Roberts, Richard J
Comstock, Laurie E
Geva-Zatorsky, Naama
Analysis of a phase-variable restriction modification system of the human gut symbiont Bacteroides fragilis
title Analysis of a phase-variable restriction modification system of the human gut symbiont Bacteroides fragilis
title_full Analysis of a phase-variable restriction modification system of the human gut symbiont Bacteroides fragilis
title_fullStr Analysis of a phase-variable restriction modification system of the human gut symbiont Bacteroides fragilis
title_full_unstemmed Analysis of a phase-variable restriction modification system of the human gut symbiont Bacteroides fragilis
title_short Analysis of a phase-variable restriction modification system of the human gut symbiont Bacteroides fragilis
title_sort analysis of a phase-variable restriction modification system of the human gut symbiont bacteroides fragilis
topic Molecular Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7641763/
https://www.ncbi.nlm.nih.gov/pubmed/33045731
http://dx.doi.org/10.1093/nar/gkaa824
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