Genome Sequences of Three Novel Bacillus cereus Bacteriophages

The Bacillus cereus group is an assemblage of highly related firmicute bacteria that cause a variety of diseases in animals, including insects and humans. We announce three high-quality, complete genome sequences of bacteriophages we isolated from soil samples taken at the bases of fruit trees in Utah County, Utah. While two of the phages (Shanette and JL) are highly related myoviruses, the bacteriophage Basilisk is a siphovirus.

well as the closely related B. anthracis, B. thuringiensis, B. mycoides, B. pseudomycoides, and B. weihenstephanesis. These firmicute bacteria are commonly found in soil, but they also cause a variety of human infectious diseases. For example, when found in food, B. cereus is frequently associated with emetic and diarrheal forms of gastroenteritis (for recent reviews, see references 1 and 2). In soil, B. thuringiensis infects the insect pests of many crops (for recent reviews, see references 3 through 5). The genomes of approximately 42 B. cereus group bacteriophage and prophage genomes can be found on GenBank. While the isolation of bacteriophages may aid in the treatment of food products, understanding the structures of their genomes may further define not only the evolution of the bacteriophages themselves, but also that of their Bacillus cereus group hosts, since many of the phages have shown significant cross-infectivity (6)(7)(8). Of the 42 B. cereus group bacteriophages, 24 were isolated using B. cereus as the host. Here we announce the genome sequences of three novel B. cereus bacteriophages, Basilisk, Shanette, and JL.
The three phages were isolated using enrichment cultures of soil samples collected in and around Provo, UT, using a locally isolated host strain (B. cereus BC7003). Following at least three plaque purifications, a high-titer phage lysate was prepared and genomic DNA was extracted. Briefly, high-titer lysates were incubated with 5 g/ml RNase and 10 g/ml DNase for 30 min at 37°C and treated with 100 g/l proteinase K at 52°C for 1 h. Sequencing was accomplished using 454 pyrosequencing (Roche). Multiple contigs were formed using Newbler version 2.6 (Roche Diagnostics, Branford, CT) and CONSED version 19 (9). Assem-bly was completed and checked using Gepard 1.30 (10). Although the physical ends and the packing and replication strategies of the phage DNA were not determined, the manual finishing and overlapping contigs assembled the genome sequence into an apparently circular genome. Base one was selected using the noncoding region upstream of the terminase gene. The putative open reading frames (ORFs) of each genome were predicted and annotated using DNA Master (http://cobamide2.bio.pitt.edu). The criteria used to assign potential ORFs were GeneMark HHM and Glimmer autoannotation, BLAST alignment E values of Ͻ0.001, coding potential from GeneMark (11) using B. cereus ATCC 14579, start codon sequences, and Shine-Dalgarno (SD) scores of Ͼ200 using the Karlin position-specific scoring matrix (PSSM) for moderately to highly expressed genes. Additionally, tRNAs were predicted using the ARAGORN (12) program. From transmission electron microscopy analysis, it was determined that Shanette and JL were of the family Myoviridae and Basilisk of the family Siphoviridae.
Nucleotide sequence accession numbers. The GenBank accession numbers, sequencing fold coverages, genome sizes, numbers of putative ORFs, numbers of tRNA genes, and GC content percentages for these bacteriophages are summarized in Table 1.

ACKNOWLEDGMENTS
This research was supported by funding from the Brigham Young University Department of Microbiology and Molecular Biology and College of Life Sciences.
We appreciate the assistance of the BYU Research Instrumentation Core Facility, the BYU DNA Sequencing Center, and student researchers