Literature DB >> 27540049

Complete Genome Sequence of Bacillus thuringiensis Bacteriophage Smudge.

Jessica L Cornell1, Eileen Breslin1, Zachary Schuhmacher1, Madison Himelright1, Cassandra Berluti1, Charles Boyd1, Rachel Carson1, Elle Del Gallo1, Caris Giessler1, Benjamin Gilliam1, Catherine Heatherly1, Julius Nevin1, Bryan Nguyen1, Justin Nguyen1, Jocelyn Parada1, Blake Sutterfield1, Muruj Tukruni1, Louise Temple2.   

Abstract

Smudge, a bacteriophage enriched from soil using Bacillus thuringiensis DSM-350 as the host, had its complete genome sequenced. Smudge is a myovirus with a genome consisting of 292 genes and was identified as belonging to the C1 cluster of Bacillus phages.
Copyright © 2016 Cornell et al.

Entities:  

Year:  2016        PMID: 27540049      PMCID: PMC4991694          DOI: 10.1128/genomeA.00572-16

Source DB:  PubMed          Journal:  Genome Announc


GENOME ANNOUNCEMENT

The bacteriophage Smudge was isolated on Bacillus thuringiensis DSM-350 as the host organism from soil samples taken from the James Madison University campus in Harrisonburg, VA, in 2015 (GPS coordinates 38°44′80.81″ N, 78°86′59.41″ W) by undergraduate researchers in collaboration with the SEA-PHAGES (Science Education Alliance-Phage Hunters Advancing Genomics and Evolutionary Science) program. Because the bacterium B. thuringiensis is safe for human use, even though it is commonly used as a biopesticide, it was safe for undergraduates to use in the research lab (1). Smudge is a myovirus, as shown by the presence of contractile and extended tails. The extended tail was 49.7 ± 2.1 nm, and the contracted tail was 29.5 ± 1.5 nm. The symmetrical head diameter was 23.2 ± 2.4 nm. In this study, the sample soil was enriched using standard procedures to isolate a single phage. Phage genomic DNA was submitted to the Pittsburgh Bacteriophage Institute for Illumina Sequencing. About 50,000 reads of raw data were assembled into a single contig using Newbler (2) with 100-fold average depth of coverage. Gene prediction was completed using GeneMark (3) and Glimmer (4). Smudge was autoannotated using DNA Master (http://cobamide2.bio.pitt.edu/computer.htm) and all gene predictions were manually curated. Functions of proteins were predicted using protein BLAST (5), HHPRED, and Conserved Domains Database. The Smudge genome consisted of 162,040 bp with a 38.8% GC content. Similar to other Bacillus phages, the genome contained a direct terminal repeat of 2,820 bp determined by the occurrence of double coverage with well-defined margins in the assembled contig. Smudge is most closely related to Megatron (KJ489401), with 98% query coverage (5). This finding and similarity to other published phages place Smudge in the C1 cluster (6). The number of predicted protein-coding regions found was 292, and no tRNA genes were present, as shown by Aragorn (7). Structural proteins included tail lysins, baseplate, tail sheath, tail fiber, major capsid, terminase, and prohead protease. Genes involved in DNA replication included DNA helicase, DNA primase, and DNA polymerase. Gene regulatory proteins included sigma factors, two helix-turn-helix binding proteins, and an I-Basl protein. Seven proteins involved in nucleic acid metabolism were adenylate kinase, thymidylate synthase, exonuclease, flavodoxin, thioredoxin, and two ribonucleotide diphosphate reductase beta subunits. The genome also was predicted to contain two endolysins and a holin. There were also two types of recombination proteins, Holliday junction resolvase and recombinase A. Aside from these genes, approximately 1,500 bp in the terminal repeats were noncoding; two hypothetical proteins were predicted in the remaining portion of the terminal repeats.

Accession number(s).

The complete genome of bacteriophage Smudge is deposited in GenBank under the accession number KX156152.
  7 in total

1.  ARAGORN, a program to detect tRNA genes and tmRNA genes in nucleotide sequences.

Authors:  Dean Laslett; Bjorn Canback
Journal:  Nucleic Acids Res       Date:  2004-01-02       Impact factor: 16.971

2.  Basic local alignment search tool.

Authors:  S F Altschul; W Gish; W Miller; E W Myers; D J Lipman
Journal:  J Mol Biol       Date:  1990-10-05       Impact factor: 5.469

3.  Identifying bacterial genes and endosymbiont DNA with Glimmer.

Authors:  Arthur L Delcher; Kirsten A Bratke; Edwin C Powers; Steven L Salzberg
Journal:  Bioinformatics       Date:  2007-01-19       Impact factor: 6.937

Review 4.  Bacillus thuringiensis: a genomics and proteomics perspective.

Authors:  Mohamed A Ibrahim; Natalya Griko; Matthew Junker; Lee A Bulla
Journal:  Bioeng Bugs       Date:  2010 Jan-Feb

5.  Genomic characterization and comparison of seven Myoviridae bacteriophage infecting Bacillus thuringiensis.

Authors:  Amber Brooke Sauder; McKenzie Rea Quinn; Alexis Brouillette; Steven Caruso; Steven Cresawn; Ivan Erill; Lynn Lewis; Kathryn Loesser-Casey; Morgan Pate; Crystal Scott; Stephanie Stockwell; Louise Temple
Journal:  Virology       Date:  2016-01-14       Impact factor: 3.616

6.  GeneMark: web software for gene finding in prokaryotes, eukaryotes and viruses.

Authors:  John Besemer; Mark Borodovsky
Journal:  Nucleic Acids Res       Date:  2005-07-01       Impact factor: 16.971

7.  Optimizing information in Next-Generation-Sequencing (NGS) reads for improving de novo genome assembly.

Authors:  Tsunglin Liu; Cheng-Hung Tsai; Wen-Bin Lee; Jung-Hsien Chiang
Journal:  PLoS One       Date:  2013-07-29       Impact factor: 3.240

  7 in total
  2 in total

1.  Complete Genome Sequences of Bacillus Phages DirtyBetty and Kida.

Authors:  Kelly Flounlacker; Rachel Miller; Diana Marquez; Allison Johnson
Journal:  Genome Announc       Date:  2017-03-09

2.  Genome Sequence of Bacillus Phage Saddex.

Authors:  Elizabeth Greguske; Alexis Nadeau; Emily Fitzmeyer; Karolina Fucikova
Journal:  Microbiol Resour Announc       Date:  2018-09-20
  2 in total

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