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. 2018 Feb 1;6(5):e01223-17. doi: 10.1128/genomeA.01223-17

Draft Genome Sequences of 11 Salmonella enterica Serovar Typhimurium Strains Isolated from Human Systemic and Nonsystemic Sites in Brazil

Pedro Henrique N Panzenhagen a,b, Narayan C Paul a, Carlos A Conte Junior b,d,e, Renata G Costa c, Dália P Rodrigues c, Devendra H Shah a,
PMCID: PMC5794934  PMID: 29437087

ABSTRACT

Salmonella enterica serovar Typhimurium strains isolated from systemic sites outside sub-Saharan Africa have been rarely sequenced. Here, we report the draft genome sequences of S. Typhimurium sequence type 19 (ST19) (n = 9), ST1649 (n = 1), and ST313 (n = 1) strains isolated from human systemic (e.g., blood) and nonsystemic (e.g., stool and wounds) sites in Brazil.

GENOME ANNOUNCEMENT

Nontyphoidal Salmonella (NTS) is one of the major causes of diarrheal disease worldwide, with an estimated 93 million enteric infections and 155,000 deaths annually (1). However, these estimates do not include the infections caused by invasive nontyphoidal Salmonella (iNTS) enterica serovar Typhimurium sequence type 313 (ST313), which is often associated with systemic infection. S. Typhimurium ST313 strains account for >50% of the systemic infections in sub-Saharan Africa (2, 3). Two genetic lineages of S. Typhimurium ST313 have been linked with the emergence of iNTS across sub-Saharan Africa (4). In Brazil, S. Typhimurium is frequently isolated from systemic sites, such as blood and cerebrospinal fluid (CSF), from human patients (5, 6); however, the genetic underpinning of S. Typhimurium isolates recovered from systemic sites in Brazil remains unknown. We sequenced 11 S. Typhimurium strains isolated from blood (n = 4), stool (n = 4), and extraintestinal (n = 3) sites between 2010 and 2014 from different geographic regions of Brazil (Table 1).

TABLE 1 .

GenBank accession numbers of Salmonella Typhimurium strains isolated from human clinical samples in Brazil

Strain SRA accession no. WGS accession no.a No. of contigs N50 (bp) Length (bp) Sourceb Yr State
PP_BR007 SAMN05505504 NPJP00000000 156 57,229 4,632,574 Blood 2014 Rio de Janeiro
PP_BR026 SAMN05505503 NPJQ00000000 149 62,099 4,777,031 Blood 2012 Rio Grande do Sul
PP_BR027 SAMN05505502 NPJR00000000 175 44,398 4,626,743 WS 2012 Rio Grande do Sul
PP_BR031 SAMN05505501 NPJS00000000 190 46,721 4,594,320 WS 2012 Rio Grande do Sul
PP_BR032 SAMN05505500 NPJT00000000 122 99,313 4,650,556 ABS 2012 Rio Grande do Sul
PP_BR045 SAMN05505499 NPJU00000000 147 76,702 4,827,606 RS 2011 Santa Catarina
PP_BR057 SAMN05505498 NRDL00000000 131 103,073 4,787,663 Blood 2011 Amapá
PP_BR060 SAMN05505496 NPMT00000000 123 96,334 4,776,943 Feces 2011 Minas Gerais
PP_BR062 SAMN05505495 NRDM00000000 118 142,310 4,958,705 Feces 2010 Santa Catarina
PP_BR063 SAMN05505494 NRDN00000000 161 50,016 4,365,189 Blood 2010 Rio Grande do Sul
PP_BR076 SAMN05505493 NSDQ00000000 125 120,490 5,065,902 Feces 2010 Rio Grande do Sul
a

WGS, whole-genome sequencing.

b

WS, wound secretion; ABS, abdominal abscess; RS, rectal swab.

Paired-end sequencing libraries (2 × 250 bp) were prepared using the Nextera XT kit (Illumina, San Diego, CA) following the protocol described in the DNA library reference guide (7), size selected to be in the range of 600 to 1,000 bp (average peaks, ~800 bp), and sequenced using the MiSeq Illumina version 2 kit, according to the manufacturer’s instructions. The number of paired reads per sample ranged from 941,320 to 1,389,798. The average G+C content was 52.5% (8). De novo assembly was performed using Velvet 1.2.10 set at default for all parameters (9). Contigs were organized by aligning to the genome sequence of the reference strain S. Typhimurium LT2 (accession no. NC_003197) using Mauve multiple alignments (10). Whole-genome multilocus sequence typing was performed using EnteroBase (https://enterobase.warwick.ac.uk/). A total of three sequence types, ST19 (n = 9), ST1695 (n = 1), and ST313 (n = 1), were identified. Detailed comparative genomics analysis of these strains is currently ongoing and will be published independently. These genome sequences will provide better insights into the molecular epidemiology of invasive S. Typhimurium strains in Brazil.

Accession number(s).

The draft genome sequences are available in GenBank under the accession numbers listed in Table 1.

ACKNOWLEDGMENTS

We thank Li Zhen at the Washington Department of Health (WADOH) and Mark Allard at the FDA Center for Food Safety and Applied Nutrition (CFSAN) for sequencing the strains used in this study.

This research was funded by the Safe Food Initiative and Agricultural Animal Health Program at the Washington State University, Pullman, WA. Pedro Henrique N. Panzenhagen received scholarship support by the Doctoral Sandwich Abroad Program CAPES/PDSE at the Federal University of Rio de Janeiro.

We declare no conflicts of interest.

Footnotes

Citation Panzenhagen PHN, Paul NC, Conte Junior CA, Costa RG, Rodrigues DP, Shah DH. 2018. Draft genome sequences of 11 Salmonella enterica serovar Typhimurium strains isolated from human systemic and nonsystemic sites in Brazil. Genome Announc 6:e01223-17. https://doi.org/10.1128/genomeA.01223-17.

REFERENCES

  • 1.WHO 2016. Salmonella (non-typhoidal). World Health Organization, ; Geneva, Switzerland: http://www.who.int/mediacentre/factsheets/fs139/en/. [Google Scholar]
  • 2.Ao TT, Feasey NA, Gordon MA, Keddy KH, Angulo FJ, Crump JA. 2015. Global burden of invasive nontyphoidal salmonella disease, 2010. Emerg Infect Dis 21:941–949. doi: 10.3201/eid2106.140999 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Reddy EA, Shaw AV, Crump JA. 2010. Community-acquired bloodstream infections in Africa: a systematic review and meta-analysis. Lancet Infect Dis 10:417–432. doi: 10.1016/S1473-3099(10)70072-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Okoro CK, Barquist L, Connor TR, Harris SR, Clare S, Stevens MP, Arends MJ, Hale C, Kane L, Pickard DJ, Hill J, Harcourt K, Parkhill J, Dougan G, Kingsley RA. 2015. Signatures of adaptation in human invasive Salmonella Typhimurium ST313 populations from sub-Saharan Africa. PLoS Negl Trop Dis 9:e0003611. doi: 10.1371/journal.pntd.0003611. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Fernandes SA, Tavechio AT, Ghilardi AC, Dias AM, Almeida IA, Melo LC. 2006. Salmonella serovars isolated from humans in São Paulo State, Brazil, 1996–2003. Rev Inst Med Trop Sao Paulo 48:179–184. doi: 10.1590/S0036-46652006000400001 [DOI] [PubMed] [Google Scholar]
  • 6.de Castro FA, dos Santos VR, Martins CHG, Fernandes SA, Zaia JE, Martinez R. 2002. Prevalence and antimicrobial susceptibility of Salmonella serotypes in patients from Ribeirão Preto, São Paulo, Brazil, between 1985 and 1999. Braz J Infect Dis 6:244–251. doi: 10.1590/S1413-86702002000500005. [DOI] [PubMed] [Google Scholar]
  • 7.Illumina 2016. Nextera XT DNA library prep kit. Reference guide (15031942 v01) Illumina, San Diego, CA. [Google Scholar]
  • 8.McClelland M, Sanderson KE, Spieth J, Clifton SW, Latreille P, Courtney L, Porwollik S, Ali J, Dante M, Du F, Hou S, Layman D, Leonard S, Nguyen C, Scott K, Holmes A, Grewal N, Mulvaney E, Ryan E, Sun H, Florea L, Miller W, Stoneking T, Nhan M, Waterston R, Wilson RK. 2001. Complete genome sequence of Salmonella enterica serovar Typhimurium LT2. Nature 413:852–856. doi: 10.1038/35101614. [DOI] [PubMed] [Google Scholar]
  • 9.Zerbino DR, Birney E. 2008. Velvet: algorithms for de novo short read assembly using de Bruijn graphs. Genome Res 18:821–829. doi: 10.1101/gr.074492.107. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Darling ACE, Mau B, Blattner FR, Perna NT. 2004. Mauve: multiple alignment of conserved genomic sequence with rearrangements. Genome Res 14:1394–1403. doi: 10.1101/gr.2289704. [DOI] [PMC free article] [PubMed] [Google Scholar]

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