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

Author:

Ben-Assa Nadav1,Coyne Michael J2,Fomenkov Alexey3ORCID,Livny Jonathan4,Robins William P5,Muniesa Maite6ORCID,Carey Vincent7,Carasso Shaqed1,Gefen Tal1,Jofre Juan6,Roberts Richard J3,Comstock Laurie E2,Geva-Zatorsky Naama18ORCID

Affiliation:

1. Department of Cell Biology and Cancer Science, Rappaport Faculty of Medicine, Technion – Israel Institute of Technology, Technion Integrated Cancer Center (TICC), Haifa, 3525422 Israel

2. Division of Infectious Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA

3. New England Biolabs, 240, County Rd., Ipswich, MA, USA

4. Infectious Disease and Microbiome Program, Broad Institute of MIT and Harvard, Cambridge, MA, USA

5. Department of Microbiology, Harvard Medical School, Boston, 02115, MA, USA

6. Department of Genetics, Microbiology and Statistics, School of Biology, University of Barcelona, Avda. Diagonal 643 08028 Barcelona Spain

7. Channing Division of Network Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA

8. Canadian Institute for Advanced Research (CIFAR) Azrieli Global Scholar, MaRS Centre, West Tower 661 University Ave., Suite 505 Toronto, ON M5G 1M1, Canada

Abstract

Abstract 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.

Funder

BWH Center for Clinical and Translational Metagenomics

Spanish Ministry

Generalitat of Catalonia

Public Health Service

National Institutes of Health

National Institute of Allergy and Infectious Diseases

Generalitat of Cataluña

HFSP

EMBO

Weizmann Institute of Science

Canadian Institute for Advanced Research

Technion - Institute of Technology

Israeli Science Foundation

ICRF Acceleration

Human Frontiers Career Development Award

Applebaum family

Gutwirth award

Publisher

Oxford University Press (OUP)

Subject

Genetics

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