Genome Sequence of the Fish Pathogen Yersinia ruckeri Strain 150, Isolated from Diseased Rainbow Trout

We present here the draft genome of a pathogenic Yersinia ruckeri strain, isolated from rainbow trout (Oncorhynchus mykiss) affected by enteric redmouth disease. The chromosome has 3,826,775 bp, a GC content of 46.88%, and is predicted to contain 3,538 coding sequences. The data will be useful for comparative pathogenicity studies.

agent of enteric redmouth disease (ERM), a hemorrhagic septicemia in fish. Since its first isolation from a rainbow trout in Idaho in the 1950s (1), this microorganism has spread to many countries infecting different fish species (2), leading to significant economic losses in salmonid aquaculture.
Since the 1970s commercial vaccines against ERM, consisting of inactivated Y. ruckeri cells of serotype O1, biotype 1, have been developed. Initially, vaccination was very useful to control the appearance of the disease, but, recently, ERM outbreaks in vaccinated fish have been reported. These were produced by serotype O1, biotype 2 Y. ruckeri strains (5-7). Nowadays, a commercialized bivalent vaccine is available that includes both biotype 1 and 2 strains. Despite the effectiveness of this vaccine, it is essential to investigate the virulence factors of this pathogen (8) since new vaccines or treatments could be necessary in the future.
Presently, apart from the genome sequence of the type strain ATCC 29473, only seven draft Y. ruckeri genomes are available. These correspond to heterogeneous strains of O1 and O2 serotypes that were isolated from different hosts like rainbow trout (9), salmon (10), or channel catfish (11).
As a way to increase the knowledge of this fish pathogen, we report here the genome sequence of the serotype O1 Y. ruckeri strain 150, isolated in Denmark from an ERM-affected rainbow trout. Genomic DNA was extracted using a GenElute bacterial genomic DNA kit (Sigma Aldrich and Co.). High-throughput Illumina sequencing technology was used to conduct paired-end sequencing of genomic DNA and construct a~700-bp library with 537 Mb of raw data. The reads were assembled using the SOAPdenovo alignment tool (12) into 49 scaffolds with sizes ranging from 502 bp to 572,189 bp. The draft genome of Y. ruckeri strain 150 is 3,826,775-bp long with a GC content of 46.88%. Genome functional annotation performed with RAST (13) found 3,538 predicted coding sequences, four rRNAs, and 21 tRNAs. Using the Tandem Repeats Finder database (14), 87 tandem repeats, repeated from 2 to 8.5 times, were found. CRISPR Finder (15) did not show any clustered regularly interspaced short palindromic repeats. Also, four prophage regions where identified by PHAST (16), of which one region was intact, two regions were incomplete, and one region was questionable.
The comparative genomic analysis of Y. ruckeri annotated genomes could be useful to gain more insight into the general virulence mechanisms of this pathogen or to identify those genes responsible for host-specific adaptations. It is also possible that the comparative analysis will expose differences among strains that could justify vaccination failures.
Accession number(s). This whole-genome shotgun project has been deposited at DDBJ/ENA/GenBank under the accession number MKFJ00000000. The version described in this paper is the first version, MKFJ01000000.

ACKNOWLEDGMENT
This work was supported by the FEDER fund.