Tran Ngau Hoang, Van Nguyen Huong, Nguyen Chuong Hoang
University of Science, Vietnam National University Ho Chi Minh City, Ho Chi Minh City, Vietnam.
Ho Chi Minh City University of Industry and Trade, Ho Chi Minh City, Vietnam.
Curr Microbiol. 2025 Aug 6;82(9):441. doi: 10.1007/s00284-025-04426-4.
Biocontrol of Vibrio parahaemolyticus, a pathogen responsible for acute hepatopancreatic necrosis disease (AHPND) in shrimp, has gained attention as an alternative to antibiotics in aquaculture. In this study, a bacterial strain isolated from a coral sample was preliminarily identified as Streptomyces sp. SS162 through 16S rRNA analysis exhibiting potent antibacterial activity with a high selectivity index against V. parahaemolyticus. This activity remained stable under high temperatures, various pH conditions, UV exposure, and proteinase K treatment. Furthermore, SS162 effectively inhibited biofilm formation by V. parahaemolyticus. Strain SS162 maintained the antibacterial activity over ten consecutive generations. For genomic taxonomy and characterization, a high-quality draft genome of 6,778,597 bp for the SS162 strain was obtained using next-generation sequencing with Nanopore technology. This genome had a GC content of 74.5% and contained 5,761 protein-coding genes. The genome of Streptomyces sp. SS162 possessed 23 subsystems belonging to 24 categories revealed by the RAST system. Comparative genomic analysis using Orthovenn3 indicated that SS162 shared the highest number of gene clusters with Streptomyces fradiae ATCC 10475. The genome phylogeny and relatedness analyses suggested that Streptomyces sp. SS162 was a strain within the Streptomyces fradiae species. Importantly, AntiSMASH analysis identified 28 biosynthetic gene clusters (BGCs), many of which were predicted to produce novel secondary metabolites. The remarkable in vitro activity against V. parahaemolyticus prompted further studies employing S. fradiae SS162 for AHPND management, whereas its taxonomic characterization and BGC identification confirmed the identity and uncovered the biotechnological potential in this strain.
副溶血性弧菌是导致对虾急性肝胰腺坏死病(AHPND)的病原体,其生物防治作为水产养殖中抗生素的替代方法已受到关注。在本研究中,通过16S rRNA分析,从珊瑚样本中分离出的一株细菌初步鉴定为链霉菌属SS162,该菌株对副溶血性弧菌表现出强大的抗菌活性和高选择性指数。这种活性在高温、各种pH条件、紫外线照射和蛋白酶K处理下保持稳定。此外,SS162有效抑制了副溶血性弧菌的生物膜形成。菌株SS162连续十代保持抗菌活性。为了进行基因组分类和表征,使用纳米孔技术的下一代测序获得了SS162菌株的高质量草图基因组,大小为6,778,597 bp。该基因组的GC含量为74.5%,包含5,761个蛋白质编码基因。链霉菌属SS162的基因组拥有RAST系统揭示的属于24类的23个子系统。使用Orthovenn3进行的比较基因组分析表明,SS162与弗氏链霉菌ATCC 10475共享的基因簇数量最多。基因组系统发育和相关性分析表明,链霉菌属SS162是弗氏链霉菌种内的一个菌株。重要的是,AntiSMASH分析鉴定出28个生物合成基因簇(BGC),其中许多预计会产生新型次生代谢产物。SS162对副溶血性弧菌显著的体外活性促使进一步研究使用弗氏链霉菌SS162来管理AHPND,而其分类表征和BGC鉴定确认了该菌株的身份并揭示了其生物技术潜力。
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