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. 2019 Jan 10;8(2):e01588-18. doi: 10.1128/MRA.01588-18

Complete Genome Sequences of Five Salmonella enterica Strains Used in Inoculation Cocktails in Low-Moisture Food Storage Studies

Julie Haendiges a,b,, Susanne Keller c, Quincy Suehr c, Nathan Anderson c, Elizabeth Reed b, Jie Zheng b, Jesse D Miller a, Maria Hoffmann a
Editor: Catherine Putontid
PMCID: PMC6328678  PMID: 30643905

Survival kinetics of Salmonella enterica have been previously studied using an inoculum cocktail composed of different strains that have been associated with low-moisture foods. Here, we report the closed genome sequences of five strains of Salmonella enterica that are commonly used in these storage studies.

ABSTRACT

Survival kinetics of Salmonella enterica have been previously studied using an inoculum cocktail composed of different strains that have been associated with low-moisture foods. Here, we report the closed genome sequences of five strains of Salmonella enterica that are commonly used in these storage studies.

ANNOUNCEMENT

The incidence of salmonellosis associated with dry food products has been increasing in recent years. An aspect of public health concern is the ability of Salmonella spp. to survive on these foods (nuts, black pepper, and spices) in a low-moisture environment. Numerous studies on the survival of Salmonella enterica in dried foods have previously been published (13) using a cocktail of different strains. Here, we report the complete closed genome sequences of 5 strains commonly used in these studies, S. enterica serotype Anatum CFSAN076215 (strain 6802), isolated from peanuts; S. enterica serotype Enteritidis CFSAN076214 (strain ATCC BAA-1045), isolated from almonds; S. enterica serotype Oranienburg CFSAN076211 (strain 1839), isolated from pecans; S. enterica serotype Tennessee CFSAN076210 (strain K4643), isolated from peanut butter; and S. enterica serotype Mbandaka CFSAN076213 (strain 688538), isolated from tahini.

The isolates were cultured in Trypticase soy broth (Becton, Dickinson, Franklin Lakes, NJ, USA) overnight at 37°C. The genomic DNA was isolated using the DNeasy blood and tissue kit (Qiagen, Inc., Valencia, CA, USA). A single SMRTbell 20-kb library was prepared according to the 20-kb PacBio sample preparation protocol using the BluePippin size-selection system (Sage Science, Beverly, MA, USA). Each isolate was sequenced based on previously reported procedures on the PacBio RS II platform (Pacific Biosciences, Menlo Park, CA, USA) using a single small-molecule real-time (SMRT) cell (4). The sequencing statistics for each isolate can be found in Table 1. The genomes were de novo assembled using the Hierarchical Genome Assembly Process version 3.0 using default settings. The assembled sequences were annotated using the NCBI Prokaryotic Genomes Annotation Pipeline (PGAP) and have been deposited at DDBJ/EMBL/GenBank. The S. Anatum (CFSAN076215) chromosome size was 4,689,440 bp, with a G+C content of 52.1%, and the plasmid size was 104,123 bp, with 50.5% G+C content. The plasmid (pCFSAN076215) showed two toxin-antitoxin (TA) modules (ccdA-ccdB and higA-2–higB-2). The ccdA-ccdB TA module can lead to the formation of persister cells if induced by environmental stress. (5). The S. Oranienburg (CFSAN076211) genome size was 4,651,134 bp, with 52.1% G+C content. The S. Tennessee (CFSAN076210) chromosome size was 4,834,056 bp, with 52.2% G+C content, and the plasmid was 109,917 bp, with 50.7% G+C content. The plasmid (pCFSAN076210) has the oxidative stress gene grxA, which can be upregulated in response to preadaptation to cold stress and may provide increased protection against hydrogen peroxide (6). The S. Enteritidis (CFSAN076214) chromosome size was 4,668,874 bp, with 52.0% G+C content; plasmid 1 was 59,261 bp, with 42.1% G+C content, and plasmid 2 was 56,636 bp, with 51.6% G+C content. Plasmid 1 (pCFSAN076214_1) has vir genes associated with the type IV secretion system. Plasmid 2 (pCFSAN076214_2) has virulence genes spvA, spvB, spvC, spvD, and spvR, which have been shown to express lethal disease in BALB/c mice (7). The S. Mbandaka (CFSAN076213) genome size was 4,709,669 bp, with 52.3% G+C content.

TABLE 1.

PacBio RS sequencing statistics

Isolate name Coverage (×) Total no. of reads Avg read length (bp) N50 read length (bp)
CFSAN076210 169 90,179 12,732 16,680
CFSAN076211 115 62,043 11,025 20,045
CFSAN076213 120 69,380 10,357 18,170
CFSAN076214 162 77,741 12,017 16,680
CFSAN076215 182 77,545 13,499 26,714

Data availability.

The sequences have been deposited in GenBank under the following accession numbers (SRA accession numbers): CP033338 and CP033339 (SRR8217764) for S. Anatum, CP033344 (SRR8170031) for S. Oranienburg, CP033345 and CP033346 (SRR8170030) for S. Tennessee, CP033340, CP033341, and CP033342 (SRR8170032) for S. Enteritidis, and CP033343 (SRR8170034) for S. Mbandaka.

ACKNOWLEDGMENTS

We thank Larry Beuchat (University of Georgia, Griffin) for providing the isolates (S. Oranienburg, S. Anatum, and S. Tennessee) for use in the storage studies.

This project was supported by the U.S. FDA, Center for Food Safety and Applied Nutrition, Office of Regulatory Science, and the NSF International Applied Research Center.

REFERENCES

  • 1.Zhang Y, Keller SE, Grasso-Kelley EM. 2017. Fate of Salmonella throughout production and refrigerated storage of tahini. J Food Prot 80:940–946. doi: 10.4315/0362-028X.JFP-16-507. [DOI] [PubMed] [Google Scholar]
  • 2.Keller SE, Anderson NM, Wang C, Burbick SJ, Hildebrandt IM, Gonsalves LJ, Suehr QJ, Farakos SMS. 2018. Survival of Salmonella during production of partially sprouted pumpkin, sunflower, and chia seeds dried for direct consumption. J Food Prot 81:520–527. doi: 10.4315/0362-028X.JFP-17-318. [DOI] [PubMed] [Google Scholar]
  • 3.Farakos SMS, Pouillot R, Keller S. 2017. Salmonella survival kinetics on pecans, hazelnuts, and pine nuts at various water activities and temperatures. J Food Prot 80:879–885. doi: 10.4315/0362-028X.JFP-16-392. [DOI] [PubMed] [Google Scholar]
  • 4.Hoffmann M, Payne J, Roberts RJ, Allard MW, Brown EW, Pettengill JR. 2015. Complete genome sequence of Salmonella enterica subsp. enterica serovar Agona 46004 2-1, associated with a multistate outbreak in the United States. Genome Announc 3:e00690-15. doi: 10.1128/genomeA.00690-15. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Tripathi A, Dewan PC, Barua B, Varadarajan R. 2012. Additional role for the ccd operon of F-plasmid as a transmissible persistence factor. Proc Natl Acad Sci USA 109:12497–12502. doi: 10.1073/pnas.1121217109. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Shah J, Desai PT, Chen D, Stevens JR, Weimer BC. 2013. Preadaptation to cold stress in Salmonella enterica serovars Typhimurium increases survival during subsequence acid stress exposure. Appl Environ Microbiol 79:7281–7289. doi: 10.1128/AEM.02621-13. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Karuse M, Roudier C, Fierer J, Harwood J, Guiney D. 1991. Molecular analysis of the virulence locus of the Salmonella Dublin plasmid pSDL2. Mol Microbiol 5:307–316. doi: 10.1111/j.1365-2958.1991.tb02111.x. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

The sequences have been deposited in GenBank under the following accession numbers (SRA accession numbers): CP033338 and CP033339 (SRR8217764) for S. Anatum, CP033344 (SRR8170031) for S. Oranienburg, CP033345 and CP033346 (SRR8170030) for S. Tennessee, CP033340, CP033341, and CP033342 (SRR8170032) for S. Enteritidis, and CP033343 (SRR8170034) for S. Mbandaka.


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