key: cord-0681989-fgu1r3b5 authors: Tariq, Mohammad A.; Carding, Simon R. title: Complete Genome Sequence of a Bacteroides fragilis Bacteriophage, vB_BfrS_NCTC date: 2021-07-22 journal: Microbiology resource announcements DOI: 10.1128/mra.00548-21 sha: b8281b723bfd74cad9a73ba64f19b70380b77861 doc_id: 681989 cord_uid: fgu1r3b5 Bacteroides fragilis is an obligate anaerobe and a common gut commensal bacterium that is also an important opportunistic pathogen. Here, we present the complete genome sequence of the circularly permuted B. fragilis bacteriophage vB_BfrS_NCTC. It comprises 47,160 bp, with 69 open reading frames. The sequencing of vB_BfrS_NCTC yielded 1,012,042 clean reads, with a mean length of 129 bp. The reads had an average Phred quality score of 35, and the GC content was 39.56%. A total of 98.54% of the reads mapped back to the genome, giving a mean coverage depth of 2,793Â. The assembled genome was shown to be circularly permuted at 47,160 bp, with a GC content of 38.83%. A total of 69 ORFs, with no tRNA genes, were identified. The genome comparison was performed using the default settings of the online tool BLASTN with the nonredundant/nucleotide database (16) and showed the greatest similarity at the nucleotide level to the B. fragilis phage Barc2635 (GenBank accession number MN078104), with 92% query coverage and 97% identity. Data availability. The genome sequence of vB_BfrS_NCTC is available in GenBank under the accession number MW314138. The SRA data can be found under the accession number SRR13174062. The emergence of antimicrobial resistance in environmental strains of the Bacteroides fragilis group Selection of the active phages against B. fragilis for further study of therapeutic perspectives Genome characterization of a novel wastewater Bacteroides fragilis bacteriophage (vB_BfrS_23) and its host GB124 Trimmomatic: a flexible trimmer for Illumina sequence data Sickle: a sliding-window, adaptive, quality-based trimming tool for FastQ files FastQC: a quality control tool for high throughput sequence data SPAdes: a new genome assembly algorithm and its applications to single-cell sequencing Circlator: automated circularization of genome assemblies using long sequencing reads Aligning sequence reads, clone sequences and assembly contigs with BWA-MEM. arXiv 1303.3997v2 Genome Project Data Processing Subgroup. 2009. The Sequence Alignment/Map format and SAMtools Qualimap 2: advanced multi-sample quality control for high-throughput sequencing data The RAST server: rapid annotations using subsystems technology RASTtk: a modular and extensible implementation of the RAST algorithm for building custom annotation pipelines and annotating batches of genomes Basic local alignment search tool ARAGORN, a program to detect tRNA genes and tmRNA genes in nucleotide sequences Database resources of the National Center for Biotechnology Information This work was supported in part by the UK Biotechnology and Biological Sciences Research Council (BBSRC) and BBSRC Institute Strategic Program grant BB/R012490/1 to the Gut Microbes and Health Research Programme and its constituent projects BBS/E/F/ 000PR10353 and BBS/E/F/000PR10356 410 (S.R.C.).We thank Dave Baker and Steven Rudder for sequencing this phage at Quadram Institute Bioscience (Norwich, UK) during the coronavirus disease 2019 (COVID-19) pandemic.