Complete Genome Sequence of Bacillus megaterium Siphophage Silence

Silence is a newly isolated siphophage that infects Bacillus megaterium, a soil bacterium that is used readily in research and commercial applications. A study of B. megaterium phage Silence will enhance our knowledge of the diversity of Bacillus phages. Here, we describe the complete genome sequence and annotated features of Silence.

forming bacterium whose large cell size makes it an ideal model for research in cell morphology. It is also used commercially as a host for the production of vitamin B 12 , penicillin acylase, and amylases (1). B. megaterium bacteriophages may be a valuable tool to advance the use of this bacterium. Here, we present the genome sequence of a newly isolated B. megaterium siphophage, Silence, which was isolated on the asporogenic B. megaterium strain KM (ATCC 13632).
Bacteriophage Silence was isolated from a soil sample collected in College Station, TX. Phage DNA was sequenced in an Illumina MiSeq 250-bp paired-end run with a 550-bp insert library at the Genomic Sequencing and Analysis Facility at the University of Texas (Austin, TX). Quality-controlled trimmed reads were assembled to a single contig of circular assembly at 34.4ϫ coverage using SPAdes version 3.5.0 (2). The contig was confirmed to be complete by PCR using primers that face the upstream and downstream ends of the contig. Products from the PCR amplification of the junctions of concatemeric molecules were sequenced by Sanger sequencing (Eton Bioscience, San Diego, CA). Genes were predicted using GeneMarkS (3) and corrected using software tools available on the Center for Phage Technology (CPT) Galaxy instance (https://cpt.tamu.edu/galaxy-public/). The morphology of Silence was determined using transmission electron microscopy performed at the Texas A&M University Microscopy and Imaging Center.
Silence contains a 40,001-bp double-stranded DNA (dsDNA) genome, with a GϩC content of 38.3% and coding density of 94.3%. It contains 66 coding sequences, 33 of which have annotated functions, as determined by InterProScan and BLASTp searches (4,5). Silence was also found to infect the plasmidless B. megaterium QM B1551 derivative PV361 (6). BLASTn analysis shows that Silence has no similarity to any phages in the current GenBank database (7). Silence is predicted to use a pac-type DNA packaging mechanism based on TerL homology with the TerL proteins of phages with known packaging strategies; accordingly, it was opened to the terS gene for annotation purposes (8).
Genes related to DNA replication and recombination activities were identified, including a single-stranded DNA (ssDNA)annealing protein, dsDNA-binding proteins, DNA polymerase, helicase, and Holliday junction resolvase. The annotated genes encoding morphogenesis proteins were those for the prohead protease, major capsid protein, tape-measure protein (and related chaperones), major tail protein, and tailspike proteins. Genes whose products are involved in DNA packaging were also identified, including the small terminase, large terminase, and portal protein. Interestingly, the large terminase subunit sequence is interrupted by a group I intron encoding a homing endonuclease. A dUTPase involved in maintaining cellular dUMP levels was also identified (9). Silence encodes an FtsK/SpoIIIE-like protein. SpoIIIE is essential for sporulation and functions as a DNA translocase that moves the chromosome across the sporulation septum into the forespore (10). The function of this protein in the phage life cycle has yet to be determined.
Nucleotide sequence accession number. The genome sequence of Silence was contributed as accession no. KT001912 to GenBank.

ACKNOWLEDGMENTS
This work was supported primarily by funding from award no. EF-0949351, "Whole Phage Genomics: A Student-Based Approach," from the National Science Foundation. Additional support came from the Center for Phage Technology, an Initial University Multidisciplinary Research Initiative supported by Texas A&M University and Texas AgriLife, and from the Department of Biochemistry and Biophysics.
We thank the CPT staff for their advice and support. This announcement was prepared in partial fulfillment of the requirements for BICH464 Phage Genomics, an undergraduate course at Texas A&M University.