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. 2015 Aug 20;3(4):e00911-15. doi: 10.1128/genomeA.00911-15

Draft Genome Sequences of 19 Salmonella enterica Serovar Typhimurium [4,5:i:−] Strains Resistant to Nalidixic Acid from a Long-Term Outbreak in Italy

Massimiliano Orsini 1,, Iolanda Mangone 1, Adriano DiPasquale 1, Samuel Perticara 1, Lorena Sacchini 1, Francesca Cito 1, Simona Iannetti 1, Maurilia Marcacci 1, Massimo Ancora 1, Paolo Calistri 1, Elisabetta Di Giannatale 1, Cesare Cammà 1
PMCID: PMC4543505  PMID: 26294627

Abstract

Here, we present the draft genome sequences of 19 Salmonella enterica serovar Typhimurium monophasic variant [4,5:i:−] strains involved in a long-term salmonellosis outbreak that occurred in central Italy in 2013 to 2014.

GENOME ANNOUNCEMENT

Salmonella is a Gram-negative foodborne pathogen distributed worldwide. Even if few lineages have been detected, its antibiotic resistance pattern is very heterogeneous, spanning from multidrug-resistant to largely susceptible strains (1). According to Garcia et al. (2), two major profiles circulate in Europe, the Spanish clone and the ASSuT clone. The ASSuT clone, which is common in Italy, harbors a genomic region that confers resistance to ampicillin, streptomycin, sulfonamides, and tetracycline (3). In central Italy, in the period of September 2013 to August 2014, a non-ASSuT long-term salmonellosis outbreak was reported; the clinical isolates were epidemiologically associated with strains isolated from wastewater, while no source attribution was possible (F. Cito, F. Baldinelli, P. Calistri, E. Di Giannatale, G. Scavia, M. Orsini, S. Iannetti, L. Sacchini, I. Mangone, L. Candeloro, A. M. Conte, C. Ippoliti, C. Cammà, M. Marcacci, M. Ancora, A. M. Dionisi, S. Ocwzarek, and I. Luzzi, unpublished data). The distinctive trait of both clinical and environmental strains was the resistance to nalidixic acid; this antibiotic resistance profile is not common, and it was observed in Europe in 2011 only (4).

Nineteen strains, chosen among clinical and environmental isolates on the basis of their spatial-temporal distribution and familiar kinship, were subjected to whole-genome sequencing together with three unrelated strains as outgroups. Genomic DNA was extracted by Qiagen EasyPrep, libraries were prepared using the Hi-Q sequencing kit, and sequencing was performed on a PGM Ion Torrent platform. Raw reads were submitted to the SRA repository (5), while biosamples were registered under the project ID PRJNA266093. Reads were trimmed and assembled using a dedicated de novo workflow under the Orione framework (6) plus some ad hoc-developed python scripts; contig annotation was performed by the NCBI team using the PGAP pipeline (http://www.ncbi.nlm.nih.gov/genomes/static/Pipeline.html).

The results from the genome annotation (numbers of coding sequences [CDSs], rRNAs, and tRNAs) are summarized in Table 1, together with N50 values and GenBank accession numbers.

TABLE 1 .

Genome annotation statistics and accession numbers

BioSample accession no. No. of contigs N50 (bp) No. of CDSs No. of rRNAs No. of tRNAs GenBank accession no.
SAMN03162139 9 794,381 3,863 25 84 LDPA00000000
SAMN03162140 8 921,005 3,551 27 82 LDYH00000000
SAMN03162153 14 838,841 3,474 27 80 LECB00000000
SAMN03162151 10 478,653 3,799 25 81 LECA00000000
SAMN03162157 14 695,105 3,707 25 83 LECD00000000
SAMN03162156 12 705,141 3,825 25 82 LECC00000000
SAMN03162148 13 627,564 3,780 27 83 LFCI00000000
SAMN03162144 28 476,560 3,635 26 86 LFCH00000000
SAMN03162141 10 566,971 3,536 26 82 LFCG00000000
SAMN03162145 14 694,859 3,409 24 80 LFDZ00000000
SAMN03162146 28 435,395 3,758 26 84 LFDY00000000
SAMN03162147 11 628,011 3,719 25 79 LFDX00000000
SAMN03162150 11 723,217 3,906 25 84 LFDW00000000
SAMN03162161 14 579,418 4,114 26 85 LFGN00000000
SAMN03162155 12 628,734 3,828 23 82 LFGR00000000
SAMN03162159 20 628,218 3,891 29 82 LFGP00000000
SAMN03162162 14 579,418 3,822 25 83 LFGM00000000
SAMN03162160 11 872,758 3,678 26 80 LFGO00000000
SAMN03162158 15 695,105 3,820 24 83 LFGQ00000000

The availability of the assembled sequences allowed us to better understand antibiotic resistance mechanisms and to clarify genomic relationships among the isolates.

Nucleotide sequence accession numbers.

The sequences described here have been deposited at GenBank under the accession numbers indicated in Table 1.

ACKNOWLEDGMENT

This work was supported by the National Ministry of Public Health (MSRCTE0212).

Footnotes

Citation Orsini M, Mangone I, DiPasquale A, Perticara S, Sacchini L, Cito F, Iannetti S, Marcacci M, Ancora M, Calistri P, Di Giannatale E, Cammà C. 2015. Draft genome sequences of 19 Salmonella enterica serovar Typhimurium [4,5:i:−] strains resistant to nalidixic acid from a long-term outbreak in Italy. Genome Announc 3(4):e00911-15. doi:10.1128/genomeA.00911-15.

REFERENCES

  • 1.European Food Safety Authority 2010. Scientific opinion on monitoring and assessment of the public health risk of “Salmonella Typhimurium-like” strains. EFSA J 8:1826. doi: 10.2903/j.efsa.2010.1826. [DOI] [Google Scholar]
  • 2.García P, Hopkins KL, García V, Beutlich J, Mendoza MC, Threlfall J, Mevius D, Helmuth R, Rodicio MR, Guerra B, Med-Vet-Net WP21 Project Group . 2014. Diversity of plasmids encoding virulence and resistance functions in Salmonella enterica subsp. enterica serovar Typhimurium monophasic variant 4,[5],12:i:- strains circulating in Europe. PLoS One 9:0089635. doi: 10.1371/journal.pone.0089635 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Lucarelli C, Dionisi AM, Filetici E, Owczarek S, Luzzi I, Villa L. 2012. Nucleotide sequence of the chromosomal region conferring multidrug resistance (R-type ASSuT) in Salmonella Typhimurium and monophasic Salmonella Typhimurium strains. J Antimicrob Chemother 67:111–114. doi: 10.1093/jac/dkr391. [DOI] [PubMed] [Google Scholar]
  • 4.Abgottspon H, Zurfluh K, Nüesch-Inderbinen M, Hächler H, Stephan R. 2014. Quinolone resistance mechanisms in Salmonella enterica serovars Hadar, Kentucky, Virchow, Schwarzengrund, and 4,5,12:i:−, isolated from humans in Switzerland, and identification of a novel qnrD variant, qnrD2, in S. Hadar. Antimicrob Agents Chemother 58:3560–3563. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Leinonen R, Sugawara H, Shumway M, International Nucleotide Sequence Database Collaboration . 2011. The Sequence Read Archive. Nucleic Acids Res 39:D19–D21. doi: 10.1093/nar/gkq1019. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Cuccuru G, Orsini M, Pinna A, Sbardellati A, Soranzo N, Travaglione A, Uva P, Zanetti G, Fotia G. 2014. Orione, a Web-based framework for NGS analysis in microbiology. Bioinformatics 30:1928–1929. doi: 10.1093/bioinformatics/btu135. [DOI] [PMC free article] [PubMed] [Google Scholar]

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