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Genome Announc. 2017 March; 5(9): e01455-16.
Published online 2017 March 2. doi:  10.1128/genomeA.01455-16
PMCID: PMC5334574

Draft Genome Sequence of Five Shiga Toxin-Producing Escherichia coli Strains Isolated from Wild Deer in Japan

ABSTRACT

Shiga toxin-producing Escherichia coli (STEC) is one of the major foodborne pathogens. Having observed the wide distribution of this pathogen in wild deer, we report here the draft genome sequence of five STEC strains isolated from wild deer (Cervus nippon yesoensis) in Hokkaido, Japan.

GENOME ANNOUNCEMENT

Shiga toxin-producing Escherichia coli (STEC) represents a major issue for public health because of its capability to cause large outbreaks and the severity of the associated illnesses (1). Epidemiological data have mounted evidence for the distribution of STEC in farm animals (2), but wildlife animals such as wild deer and other cervids and birds also carry STEC (3,5). Recently, increased trends for the consumption of game meats, mainly consisting of wild deer and boar meats, in Japan (6) have made it necessary to elucidate virulence properties of STEC from these wildlife animals. As wild deer has been recognized as one of the major reservoirs (7), we obtained STEC strains 11226, 11229, 11247, 15821, and 16309 from feces of wild deer (Cervus nippon yesoensis) inhabiting Hokkaido, Japan, between 2011 and 2016. Genomic DNA of the five strains were sequenced by single-end sequencing with an Ion Torrent PGM sequencer (Thermo Fisher Scientific, Waltham, MA, USA), resulting in an average coverage of 139×. Raw reads were trimmed and de novo assembled using CLC Genomics Workbench v 9.0 (Qiagen, Hilden, Germany). The parameters for trimming were as follows: ambiguous limit, 2; quality limit, 0.05; number of 5′-terminal nucleotides, 20; number of 3′-terminal nucleotides, 5. The parameters for the de novo assembly were as follows: mapping mode, create simple contig sequences (fast); bubble size, 50; word size, 21; minimum contig length, 1,000 bp; perform scaffolding, no; autodetect paired distances, yes.

The draft genomes of the five STEC strains were assembled into 250, 246, 282, 238, and 135 contigs with an accumulated length ranging from 5,248,909 to 5,404,906 bp (N50, 140,330 bp on average) and an average G+C content of 45.5% to 50.7%. The genome was annotated by the RAST server (8). Annotation of these assemblies identified 5,161 to 5,401 coding sequences (CDSs), 70 to 79 rRNAs, and 64 to 70 tRNAs.

Their sequence types (ST) and serotypes were also identified as follows: ST32/O145:NM (11226), ST446/OUT:HUT (11229), ST11/O157:H7 (11247), ST32/O145:NM (15821), and ST5597/OUT:HUT (16309), by multilocus sequence type (MLST) 1.8 (https://cge.cbs.dtu.dk/services/) and slide agglutination testing.

Three genomes (strains 11226, 15821, and 16309) contained stx1a, and two strains, 11229 and 11247, contained stx2d, which showed 100% similarity in the nucleotide sequences to those from STEC previously isolated from wild deer (3). Other representative virulence genes, eae and ehxA, were present in three genomes (11226, 11247, and 15821). Since eae-negative STEC also cause human illness (9), we could not exclude the possibility for their potential to cause human infection. Additionally, four genomes except for strain 11229 contained astA, which is associated with the development of diarrhea (10). The data provided can aid in future efforts to identify the source of infection. Further accumulation of genomic data of the deer-originating STEC and their use for evolutional studies would also improve our understandings of the host or geographic adaptation of this pathogen.

Accession number(s).

This whole-genome shotgun project has been deposited at DDBJ/EMBL/GenBank under the GenBank accession numbers BDLI01000000 (11226), BDLJ01000000 (11229), BDLK01000000 (11247), BDLL01000000 (15821), and BDLM01000000 (16309). The versions described in this paper are the first versions, BDLI01000000 (11226), BDLJ01000000 (11229), BDLK01000000 (11247), BDLL01000000 (15821), and BDLM01000000 (16309).

ACKNOWLEDGMENTS

This work was financially supported in part by a grant from the Ministry of Health, Labour and Welfare (MHLW) (H27-shokuhin-ippan-011) and a Grant-in-Aid of Scientific Research from the Japan Society for the Promotion of Science (JSPS) (16K08040).

Footnotes

Citation Asakura H, Ikeda T, Yamamoto S, Kabeya H, Sugiyama H, Takai S. 2017. Draft genome sequence of five Shiga toxin-producing Escherichia coli strains isolated from wild deer in Japan. Genome Announc 5:e01455-16. https://doi.org/10.1128/genomeA.01455-16.

REFERENCES

1. Tarr PI, Gordon CA, Chandler WL 2005. Shiga-toxin-producing Escherichia coli and haemolytic uraemic syndrome. Lancet 365:1073–1086. doi:.10.1016/S0140-6736(05)71144-2 [PubMed] [Cross Ref]
2. Persad AK, LeJeune JT 2014. Animal reservoirs of Shiga toxin-producing Escherichia coli. Microbiol Spectr 2:EHEC-0027-2014. [PubMed]
3. Asakura H, Makino S, Shirahata T, Tsukamoto T, Kurazono H, Ikeda T, Takeshi K 1998. Detection and genetical characterization of Shiga toxin-producing Escherichia coli from wild deer. Microbiol Immunol 42:815–822. doi:.10.1111/j.1348-0421.1998.tb02356.x [PubMed] [Cross Ref]
4. Franklin AB, Vercauteren KC, Maguire H, Cichon MK, Fischer JW, Lavelle MJ, Powell A, Root JJ, Scallan E 2013. Wild ungulates as disseminators of Shiga toxin-producing Escherichia coli in urban areas. PLoS One 8:e81512. doi:.10.1371/journal.pone.0081512 [PMC free article] [PubMed] [Cross Ref]
5. Makino S, Kobori H, Asakura H, Watarai M, Shirahata T, Ikeda T, Takeshi K, Tsukamoto T 2000. Detection and characterization of Shiga toxin-producing Escherichia coli from seagulls. Epidemiol Infect 125:55–61. doi:.10.1017/S0950268899004100 [PubMed] [Cross Ref]
6. Japan Ministry of Environments 2014. Protection and control of wild birds and mammals and hunting management act. (http://law.e-gov.go.jp/htmldata/H14/H14HO088.html) Accessed: 15 October 2016.
7. Miko A, Pries K, Haby S, Steege K, Albrecht N, Krause G, Beutin L 2009. Assessment of Shiga toxin-producing Escherichia coli isolates from wildlife meat as potential pathogens for humans. Appl Environ Microbiol 75:6462–6470. doi:.10.1128/AEM.00904-09 [PMC free article] [PubMed] [Cross Ref]
8. Aziz RK, Bartels D, Best AA, DeJongh M, Disz T, Edwards RA, Formsma K, Gerdes S, Glass EM, Kubal M, Meyer F, Olsen GJ, Olson R, Osterman AL, Overbeek RA, McNeil LK, Paarmann D, Paczian T, Parrello B, Pusch GD, Reich C, Stevens R, Vassieva O, Vonstein V, Wilke A, Zagnitko O 2008. The RAST Server: rapid annotations using subsystems technology. BMC Genomics 9:75. doi:.10.1186/1471-2164-9-75 [PMC free article] [PubMed] [Cross Ref]
9. Lorenz SC, Kotewicz ML, Hoffmann M, Gonzalez-Escalona N, Fischer M, Kase JA 2016. Complete genome sequences of four enterohemolysin-positive (ehxA) enterocyte effacement-negative Shiga toxin-producing Escherichia coli strains. Genome Announc 4(5):e00846-16. doi:.10.1128/genomeA.00846-16 [PMC free article] [PubMed] [Cross Ref]
10. Weiglmeier PR, Rösch P, Berkner H 2010. Cure and curse: E. coli heat-stable enterotoxin and its receptor guanylyl cyclase c. Toxins 2:2213–2229. doi:.10.3390/toxins2092213 [PMC free article] [PubMed] [Cross Ref]

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