Literature DB >> 26227606

Draft Genome Sequences of Human-Pathogenic Escherichia coli O26:H11 Strains Carrying the stx2 Gene Only and Circulating in France.

Sabine Delannoy1, Patricia Mariani-Kurkdjian2, Stephane Bonacorsi2, Sandrine Liguori3, Sarah A Ison4, Patrick Fach5.   

Abstract

Shiga toxin-producing Escherichia coli (STEC) O26:H11 is one of the most frequent pathogens associated with diarrhea and hemolytic-uremic syndrome (HUS). In this report, we present the draft genome sequences of seven strains of STEC O26:H11 carrying the stx2a or stx2d gene only and isolated in France from HUS patients.
Copyright © 2015 Delannoy et al.

Entities:  

Year:  2015        PMID: 26227606      PMCID: PMC4520904          DOI: 10.1128/genomeA.00852-15

Source DB:  PubMed          Journal:  Genome Announc


GENOME ANNOUNCEMENT

Among Shiga toxin-producing Escherichia coli (STEC) isolates, serotype O26:H11 is the second most frequently associated with severe human diseases worldwide, after O157:H7 (1, 2). Strains of STEC O26:H11 usually harbor the stx1a gene only or in combination with stx2a. However, in the 1990s, a new clonal subgroup of STEC O26 emerged that carries the stx2a gene alone (3). This new clone, first described in Germany, has spread over Europe and has recently been described on the American continent (4, 5). In a previous study (6), we analyzed 23 STEC O26 strains carrying the stx2 gene only, which were isolated in France between 2010 and 2013 from hemolytic-uremic syndrome (HUS) patients. Although most of the strains appeared to correspond to this new clone, 12 of them exhibited significantly different characteristics. In order to investigate more thoroughly the genetic relationship between the different clones, we sequenced seven of these strains covering the different combination observed between sequence types (ST), stx gene subtype, and virulence gene profile. Genomic DNA was extracted from an overnight culture in tryptic soy broth (TSB) medium using the DNeasy blood and tissue kit (Qiagen), with an additional RNase A (Roche) treatment. Libraries were prepared using the Nextera XT kit (Illumina). Whole-genome sequencing was performed using an Illumina MiSeq platform (Illumina), according to the manufacturer’s instructions. Two MiSeq runs were carried out, one with paired-end 150-nucleotide (nt) reads on MiSeq V2 microchemistry and another with paired-end 300-nt reads on V3 chemistry. The raw reads were trimmed (minimum length, 35 bp; quality score, 0.03) and assembled in CLC Genomics Workbench 7.5.1 by de novo assembly (minimum contig length, 1,000 bp), producing 192 to 223 contigs (Table 1). The median read depth of the assemblies ranged from 38× for 34827 and 34870 to 84× for 36708, with an N50 between 65 kbp and 114 kbp (Table 1). The sequences were annotated using the National Center for Biotechnology Information (NCBI) Prokaryotic Genomes Automatic Annotation Pipeline (PGAAP) at http://www.ncbi.nlm.nih.gov/genomes/static/Pipeline.html.
TABLE 1 

NCBI accession numbers and assembly metrics of the O26:H11 E. coli draft genomes

IsolateSTstx subtypeNo. of contigsGenome size (bp)N50 (bp)Median read depth (×)No. of coding sequences (per PGAAP)NCBI accession no.
36084ST21stx2a2055,235,00796,218455,209LDXI00000000
36708ST29stx2a1925,526,827114,644845,579LDXG00000000
34827ST29stx2a2235,604,04473,150385,674LDXF00000000
34870ST29stx2a1965,498,01065,024385,524LDXE00000000
36348ST29stx2d2085,570,46794,008715,573LDXD00000000
36293ST29stx2d2075,458,92375,621455,460LDXC00000000
36493ST29stx2d2045,422,92978,448475,389LDXB00000000
NCBI accession numbers and assembly metrics of the O26:H11 E. coli draft genomes The average size of the genomes in this study is 5.47 Mb, with 5.23 Mb being the smallest genome size (isolate 36084, Table 1) and 5.60 Mb the largest genome size (isolate 34827, Table 1). On average, 5,487 coding sequences were identified in the genomes (Table 1). BLAST analysis of the stx genes confirmed the previously identified subtypes (Table 1). A detailed report on further analyses of the draft genome sequences will be released in a future publication.

Nucleotide sequence accession numbers.

The annotated draft whole-genome sequences of these O26:H11 strains were deposited in DDBJ/ENA/GenBank under the accession numbers LDXB00000000 to LDXG00000000 and LDXI00000000 (Table 1). The versions described in this paper are the first versions, LDXB01000000 to LDXG01000000 and LDXI01000000.
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