Abstract
We present the draft genome sequence of Aeromonas salmonicida subsp. achromogenes strain AS03, an atypical A. salmonicida strain that causes erythrodermatitis in crucian carp (Carassius carassius). This is the first genome sequence report of A. salmonicida subsp. achromogenes, one of the four subspecies of atypical A. salmonicida.
GENOME ANNOUNCEMENT
Aeromonas salmonicida is a fish pathogen that causes furunculosis and other related diseases, and it is responsible for significant economic loss in the aquaculture industry (1–3). Five subspecies within A. salmonicida have been described: A. salmonicida subsp. salmonicida, A. salmonicida subsp. achromogenes, A. salmonicida subsp. masoucida, A. salmonicida subsp. smithia, and A. salmonicida subsp. pectinolytica (3, 4). A. salmonicida subsp. salmonicida is referred to as typical, whereas the other A. salmonicida strains are referred to as atypical (5).
The A. salmonicida subsp. achromogenes isolate AS03, which was collected from an ulcer in a crucian carp (Carassius carassius), was previously confirmed as A. salmonicida subsp. achromogenes (6), and genomic DNA was isolated using the DNeasy blood and tissue kit (Qiagen, Valencia, CA). Draft genome sequencing was performed using the Roche/454 pyrosequencing method on the Genome Sequencer FLX system with Titanium chemistry at Macrogen in Korea (21× coverage). Putative open reading frames (ORFs) were predicted using the Web-based NCBI Glimmer 3 tool (7), and translated ORFs were then compared to known protein sequences using BLAST (8). Gene ontology (GO) databases were additionally used to functionally classify the ORFs.
The 160,381 reads generated, with a length of 101,019,529 bp, were then assembled using de novo software (version 2.6). This assembly generated 69 large (>500 bp) contigs, with a length of 4,958,383 bp. The N50 contig length is 124,543 bp, and the largest contig assembled was 247,214 bp. The average contig size is 71,860 bp. The reads were assembled into 9 scaffolds with a length of 5,018,830 bp. The N50 scaffold was 2,773,112 bp, and the average length of the scaffolds is 557,647 bp.
The GO results revealed that 36%, 34%, and 9% of sequences included genes related to biological processes, molecular functions, and cellular components, respectively. In the GO category of biological processes, “metabolic processes” was the predominant subcategory, representing 33% of the genes. In the cellular component category, 48% of the genes were annotated as unknown, but 23% and 17% of the genes were associated with cell parts and membrane, respectively. Based on their molecular function, 48% of the genes were identified as being associated with catalytic activity.
Until now, some genome sequence data for typical A. salmonicida subsp. salmonicida strains, such as 01-B526 (9) and A449 (10), have been reported, but there have been no data for atypical A. salmonicida strains that cause atypical furunculosis and other related diseases in fish.
Nucleotide sequence accession number.
The nucleotide sequence for the draft genome was deposited in GenBank under the accession no. AMQG00000000.
ACKNOWLEDGMENT
This research was supported by the Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education (2013R1A1A2006794).
Footnotes
Citation Han JE, Kim JH, Shin SP, Jun JW, Chai JY, Park SC. 2013. Draft genome sequence of Aeromonas salmonicida subsp. achromogenes AS03, an atypical strain isolated from crucian carp (Carassius carassius) in the Republic of Korea. Genome Announc. 1(5):e00791-13. doi:10.1128/genomeA.00791-13.
REFERENCES
- 1. Bernoth EM. 1997. Furunculosis: the history of the disease and of disease research, p 1–20 In Bernoth EM, Ellis AE, Midtlyng P, Olivier G, Smith P. (ed), Furunculosis: multidisciplinary fish disease research. Academic Press, London, United Kingdom [Google Scholar]
- 2. Hiney M, Olivier G. 1999. Furunculosis (Aeromonas salmonicida), p 341–425 In Woo PTK, Bruno DW. (ed), Fish diseases and disorders, vol III: viral, bacterial and fungal infections. CAB, Oxford, United Kingdom [Google Scholar]
- 3. Wiklund T, Dalsgaard I. 1998. Occurrence and significance of atypical Aeromonas salmonicida in non-salmonid and salmonid fish species: a review. Dis. Aquat. Organ. 32:49–69 [DOI] [PubMed] [Google Scholar]
- 4. Pavan ME, Abbott SL, Zorzopulos J, Janda JM. 2000. Aeromonas salmonicida subsp. pectinolytica subsp. nov., a new pectinase-positive subspecies isolated from a heavily polluted river. Int. J. Syst. Evol. Microbiol. 50:1119–1124 [DOI] [PubMed] [Google Scholar]
- 5. Gudmundsdottir BK, Bjornsdottir B. 2007. Vaccination against atypical furunculosis and winter ulcer disease of fish. Vaccine 25:5512–5523 [DOI] [PubMed] [Google Scholar]
- 6. Kim JH, Hwang SY, Son JS, Han JE, Jun JW, Shin SP, Choresca CH, Choi YJ, Park YH, Park SC. 2011. Molecular characterization of tetracycline and quinolone-resistant Aeromonas salmonicida isolated in Korea. J. Vet. Sci. 12:41–48 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7. Delcher AL, Bratke KA, Powers EC, Salzberg SL. 2007. Identifying bacterial genes and endosymbiont DNA with Glimmer. Bioinformatics 23:673–679 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8. Altschul SF, Madden TL, Schaffer AA, Zhang J, Zhang Z, Miller W, Lipman DJ. 1997. Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res. 25:3389–3402 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9. Charette SJ, Brochu F, Boyle B, Filion G, Tanaka KH, Derome N. 2012. Draft genome sequence of the virulent strain 01-B526 of the fish pathogen Aeromonas salmonicida. J. Bacteriol. 194:722–723 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10. Reith ME, Singh RK, Curtis B, Boyd JM, Bouevitch A, Kimball J, Munholland J, Murphy C, Sarty D, Williams J, Nash JHE, Johnson SC, Brown LL. 2008. The genome of Aeromonas salmonicida subsp. salmonicida A449: insights into the evolution of a fish pathogen. BMC Genomics 9:427. 10.1186/1471-2164-9-427 [DOI] [PMC free article] [PubMed] [Google Scholar]