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Journal of Bacteriology logoLink to Journal of Bacteriology
. 2012 Dec;194(23):6644–6645. doi: 10.1128/JB.01759-12

Draft Genome Sequence of the Fish Pathogen Vibrio harveyi Strain ZJ0603

Yucong Huang a,b, Jichang Jian a,b, Yishan Lu a,b, Shuanghu Cai a,b, Bei Wang a,b, Jufen Tang a,b, Huanying Pang a,b, Yu Ding a,b, Zaohe Wu b,c,
PMCID: PMC3497516  PMID: 23144396

Abstract

Vibrio harveyi is an important pathogen that causes vibriosis in various aquatic organisms. Here, we announce the draft genome sequence of V. harveyi strain ZJ0603, which was isolated from diseased Orange-spotted grouper (Epinephelus coioides) in Guangdong, China.

GENOME ANNOUNCEMENT

Vibrio harveyi has been identified as an opportunistic pathogen that causes serious production losses in marine fish farms, with mortality up to 100%, particularly in juvenile populations (9). In addition to marine fish, V. harveyi is also an important agent capable of infecting a wide range of aquatic animals, including shrimp, seahorse, bivalves, cephalopods, and elasmobranches (1). V. harveyi has caused recurrent outbreaks of the form of vibriosis known as “skin ulcer disease” in Orange-spotted grouper (Epinephelus coioides) in Guangdong Province of China since 2008 (8). To date, although a number of virulence-related genes have been identified in V. harveyi, the pathogenic mechanism of V. harveyi remains unclear (7). It is known that quorum-sensing systems, lipopolysaccharide, and extracellular products, including alkaline proteases, metalloproteases, and hemolysins, are involved in V. harveyi infection (5). It is generally believed that genome sequence information could greatly strengthen our understanding of the molecular pathogenic mechanisms of V. harveyi. Here, we report the complete genome sequence of V. harveyi strain ZJ0603, which was isolated from diseased Orange-spotted grouper after a vibriosis outbreak in Guangdong Province, China.

Genomic DNA was isolated from overnight cultures by using a Wizard genomic DNA purification kit (Fermentas MBI, Hanover, MD). The genomes were sequenced by Beijing Genomics Institute (BGI; Shenzhen, China) by using high-throughput paired-end Illumina sequencing technology, according to the manufacturer's instructions, with 98-fold coverage. Sequencing libraries were constructed according to the manufacturer's instructions. The GAII paired-end reads were assembled into genomic sequences using the SOAP de novo program, an in-house assembler based on de Bruijn graph-based sequence assembly methods, and gaps were filled by mapping information (6). Gene prediction and annotation were carried out using Glimmer3 (4), the RAST annotation server (2), and the NCBI COG database. A total of 65 scaffolds containing 206 contigs were obtained, with a total length of 6,697,981 bp. A total of 6,326 genes were discovered, with an average GC content of 44.63%. The number of ribosomal genes was 97, including 94 tRNAs and 3 rRNAs.

A variety of genes related to iron acquisition, virulence, and environmental adaption were identified in this genome, such as hemolysins, proteases, chitinases, collagenases, RTX toxins, and vibriolysin, as well as some iron transport genes. The genome sequence analysis also revealed several protein secretion systems, including type I, II, III, IV, and VI secretion systems and a Flp-type pilus system. The latter has been proposed to represent a new subtype of type II secretion systems and is essential for motility, biofilm formation, and colonization (3). The presence of these genes is involved in the organism's pathogenicity and confers a fitness advantage to marine bacteria, increasing long-term survival in the marine environment. The content of the genome also revealed genes associated with stress responses, including osmotic and oxidative stress, cold and heat shock, and detoxification.

Nucleotide sequence accession numbers.

The whole-genome shotgun sequence of V. harveyi strain ZJ0603 has been deposited in the GenBank database under accession number AKIH00000000. The version described in this study is the first version, with accession number AKIH01000000.

ACKNOWLEDGMENTS

This study was supported by the National Basic Research Program of China (number 2009CB118704), the 973 Program Earlier Research Project (number 2011CB111601), and the Guangdong Provincial Science and Technology Plan (numbers 2008A020100014 and 2009B050700040).

We thank all the people who have dedicated time to these experiments.

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