Institute of Bioinformatics and Biosignal Transduction, College of Bioscience and Biotechnology, National Cheng Kung University, Tainan 701, Taiwan.
Graduate Institute of Cancer Biology and Drug Discovery, College of Medical Science and Technology, Taipei Medical University, Taipei 110, Taiwan.
Mar Drugs. 2017 Dec 1;15(12):373. doi: 10.3390/md15120373.
In aquaculture, shrimp farming is a popular field. The benefits of shrimp farming include a relatively short grow-out time, high sale price, and good cost recovery. However, outbreaks of serious diseases inflict serious losses, and acute hepatopancreatic necrosis disease (AHPND) is an emerging challenge to this industry. In South American white shrimp () and grass shrimp (), this disease has a 70-100% mortality. The pathogenic agent of AHPND is a specific strain of which contains PirA and PirB toxins encoded in the pVA1 plasmid. PirA and PirB have been shown to cause the typical histological symptoms of AHPND in infected shrimps, and in this review, we will focus on our structural understanding of these toxins. By analyzing their structures, a possible cytotoxic mechanism, as well as strategies for anti-AHPND drug design, is proposed.
在水产养殖中,虾养殖是一个热门领域。虾养殖的好处包括相对较短的养殖时间、高销售价格和良好的成本回收。然而,严重疾病的爆发会造成严重的损失,急性肝胰腺坏死病(AHPND)是该行业面临的一个新挑战。在南美白对虾()和草虾()中,这种疾病的死亡率高达 70-100%。AHPND 的病原体是一种特定的菌株,它包含在 pVA1 质粒中编码的 PirA 和 PirB 毒素。已经表明,PirA 和 PirB 会导致感染虾出现 AHPND 的典型组织学症状,在这篇综述中,我们将重点介绍我们对这些毒素的结构理解。通过分析它们的结构,提出了一种可能的细胞毒性机制,以及抗 AHPND 药物设计的策略。