| Autor: |
Hamilton TA; Department of Biochemistry, Schulich School of Medicine & Dentistry, Western University, London N6A 5C1, ON, Canada., Joris BR; Department of Biochemistry, Schulich School of Medicine & Dentistry, Western University, London N6A 5C1, ON, Canada., Shrestha A; Department of Biochemistry, Schulich School of Medicine & Dentistry, Western University, London N6A 5C1, ON, Canada., Browne TS; Department of Biochemistry, Schulich School of Medicine & Dentistry, Western University, London N6A 5C1, ON, Canada., Rodrigue S; Départment de Biologie, Université de Sherbrooke, Sherbrooke J1K 2R1, QC, Canada., Karas BJ; Department of Biochemistry, Schulich School of Medicine & Dentistry, Western University, London N6A 5C1, ON, Canada., Gloor GB; Department of Biochemistry, Schulich School of Medicine & Dentistry, Western University, London N6A 5C1, ON, Canada., Edgell DR; Department of Biochemistry, Schulich School of Medicine & Dentistry, Western University, London N6A 5C1, ON, Canada. |
| Abstrakt: |
Metagenomic sequences represent an untapped source of genetic novelty, particularly for conjugative systems that could be used for plasmid-based delivery of Cas9-derived antimicrobial agents. However, unlocking the functional potential of conjugative systems purely from metagenomic sequences requires the identification of suitable candidate systems as starting scaffolds for de novo DNA synthesis. Here, we developed a bioinformatics approach that searches through the metagenomic "trash bin" for genes associated with conjugative systems present on contigs that are typically excluded from common metagenomic analysis pipelines. Using a human metagenomic gut data set representing 2805 taxonomically distinct units, we identified 1598 contigs containing conjugation genes with a differential distribution in human cohorts. We synthesized de novo an entire Citrobacter spp. conjugative system of 54 kb containing at least 47 genes and assembled it into a plasmid, pCitro. We found that pCitro conjugates from Escherichia coli to Citrobacter rodentium with a 30-fold higher frequency than to E. coli , and is compatible with Citrobacter resident plasmids. Mutations in the traV and traY conjugation components of pCitro inhibited conjugation. We showed that pCitro can be repurposed as an antimicrobial delivery agent by programming it with the TevCas9 nuclease and Citrobacter -specific sgRNAs to kill C. rodentium . Our study reveals a trove of uncharacterized conjugative systems in metagenomic data and describes an experimental framework to animate these large genetic systems as novel target-adapted delivery vectors for Cas9-based editing of bacterial genomes. |
