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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...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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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. |
format | Online Article Text |
id | pubmed-7641763 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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