Abstract
Salmonella enterica subsp. enterica serovar Thompson strain RM6836 was isolated from lettuce in 2002. We report here the complete sequence and annotation of the genome of S. Thompson RM6836. This is the first reported complete genome sequence for S. Thompson and it will enhance our understanding of this serovar and provide another point for comparative studies between Salmonella enterica strains.
GENOME ANNOUNCEMENT
Salmonella enterica subsp. enterica is a major cause of food-borne illnesses associated with a wide variety of foods, including meat, eggs, fruits, vegetables, nuts, and spices. Based on the serologic identification of O (lipopolysaccharide) and H (flagellar) antigens, S. enterica subsp. enterica has been classified into a variety of groups and specific serovars (1). Among S. enterica subsp. enterica strains, the most common O-antigen serogroups are A, B, C1, C2, D, and E, and these serogroups cause approximately 99% of Salmonella infections in humans (1). S. enterica subsp. enterica serovar Thompson is in serogroup C1 and has been the cause of food-borne outbreaks associated with cilantro, arugula, chicken, beef, bread, and smoked salmon (2, 4–8). S. Thompson strain RM6836 was isolated from lettuce in 2002 and serotyped by the FDA Center for Veterinary Medicine as part of the USDA, Agricultural Marketing Service, Microbiological Data Program.
Genome sequencing was performed using shotgun and paired-end (8 to 12 kb) libraries and was generated on a Roche 454 FLX+ sequencing system with Titanium chemistry. The Roche Newbler assembler (version 2.3) was used to assemble 187,876 shotgun and 103,498 paired-end reads into 64 contigs and a single scaffold. Genome closing utilized a combination of steps. The contigs were aligned to the other genomes of S. enterica subsp. enterica, including serovar Typhimurium LT2 and serovar Enteritidis strain P125109, using the software Mauve (3) to find unexpected gaps. Scaffold gaps were filled by a combination of referenced assemblies of 1,907,370 Illumina MiSeq reads to the Newbler contigs using Geneious version 6.1.6 and the identification of repeated contigs using the Perlscript contig_extender2. Certain gaps were validated using PCR amplification and Sanger sequencing. All base calls were validated using the Illumina MiSeq reads, which provided an additional 100× coverage.
The S. Thompson RM6836 genome size is 4,707,648 bp, with a G+C content of 52.2%. The genome sequence was annotated using the NCBI Prokaryotic Genomes Automatic Annotation Pipeline (PGAAP) (http://www.ncbi.nlm.nih.gov/genomes/static/Pipeline.html) and was deposited with GenBank. The RM6836 genome is predicted to carry 4,621 genes, 7 ribosomal RNA operons, and 79 tRNAs. Bacteriophages were identified using PHAST (9), including one identified as Gifsy 1 and four remnant prophages. The S. Thompson RM6836 genome is highly syntenic to other S. enterica subsp. enterica serovars, with variable positions of prophage and bacteriophage remnants in the different serovars. RM6836 does not possess a virulence plasmid, which is common to many other S. enterica subsp. enterica strains. To our knowledge, this is the first complete S. Thompson genome sequence to be released into the public domain.
Nucleotide sequence accession number.
The S. Thompson RM6836 genome sequence has been deposited in GenBank under the accession no. CP006717.
ACKNOWLEDGMENTS
We thank Shanker Reddy and Michelle Sipe at USDA AMS for strain RM6836 collected during the USDA AMS Microbial Data Program. We thank William Miller for his Perlscript contig_extender2 and Kerry Cooper for discussion of assembly methods. We also thank Robert Mandrell and Anne Bates for curation of the Produce Safety and Microbiology Research Unit strain collection.
This work was supported by the United States Department of Agriculture, Agricultural Research Service CRIS project no. 5325-42000-047.
Footnotes
Citation Parker CT, Gorski L, Huynh S. 2013. Complete genome sequence of Salmonella enterica subsp. enterica serovar Thompson strain RM6836. Genome Announc. 1(6):e00900-13. doi:10.1128/genomeA.00900-13.
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