Genomic characterization and identification of virulence-related genes in Vibrio nigripulchritudo isolated from white leg shrimp Penaeus vannamei.
Jayasundara Mudiyanselage Sajani Nisansala RathnapalaWafaa RagabSatoshi KawatoMiho FurukawaReiko NozakiHidehiro KondoIkuo HironoPublished in: Journal of fish diseases (2023)
Vibrio nigripulchritudo causes vibriosis in penaeid shrimps. Here, we used Illumina and Nanopore sequencing technologies to sequence the genomes of three of its strains (TUMSAT-V. nig1, TUMSAT-V. nig2, and TUMSAT-V. nig3) to explore opportunities for disease management. Putative virulence factors and mobile genetic elements were detected while evaluating the phylogenetic relationship of each isolated strain. The genomes consisted of two circular chromosomes (I and II) plus one or two plasmids. The size of chromosome I ranged from 4.02 to 4.07 Mb with an average GC content of 46%, while the number of predicted CDSs ranged from 3563 to 3644. The size of chromosome II ranged from 2.16 to 2.18 Mb, with an average GC content of 45.5%, and the number of predicted CDSs ranged from 1970 to 1987. Numerous virulence genes were identified related to adherence, antiphagocytosis, chemotaxis, motility, iron uptake, quorum sensing, secretion systems, and toxins in all three genomes. Higher numbers of prophages and genomic islands found in TUMSAT-V. nig1 suggest that the strain has experienced numerous horizontal gene transfer events. The presence of antimicrobial resistance genes suggests that the strains have multidrug resistance. Comparative genomic analysis showed that all three strains belonged to the same clade.
Keyphrases
- antimicrobial resistance
- escherichia coli
- copy number
- biofilm formation
- genome wide
- bioinformatics analysis
- dna methylation
- pseudomonas aeruginosa
- genome wide identification
- staphylococcus aureus
- klebsiella pneumoniae
- candida albicans
- gas chromatography
- single cell
- single molecule
- mass spectrometry
- gene expression
- type diabetes
- weight loss
- high resolution
- skeletal muscle
- tandem mass spectrometry
- glycemic control