Aquaculture Pathology Laboratory, School of Animal and Comparative Biomedical Sciences, The University of Arizona, AZ. 85721, USA.
Aquaculture Pathology Laboratory, School of Animal and Comparative Biomedical Sciences, The University of Arizona, AZ. 85721, USA.
Mol Cell Probes. 2019 Feb;43:20-28. doi: 10.1016/j.mcp.2018.12.004. Epub 2018 Dec 18.
Acute hepatopancreatic necrosis disease (AHPND), also known as Early mortality syndrome (EMS), is a recently emerged lethal disease that has caused major economic losses in shrimp aquaculture. The etiologic agents are Vibrio spp. that carry Photorhabdus Insect-Related (Pir) toxin genes pirA and pirB. A multiplex SYBR Green real-time PCR was developed that detects pirA, pirB, and two internal control genes, the shrimp 18S rRNA and the bacterial 16S rRNA genes in a single reaction. The pirB primers amplify the 3'-end of the pirB gene allowing the detection of Vibrio spp. mutants that contain a complete deletion of pirA and the partial deletion of pirB. The assay also detects mutants that contain the entire pirA gene and the deletion of the pirB gene. Since both toxin genes are needed for disease development, this assays can distinguish between pathogenic strains of Vibrio spp. that cause AHPND in shrimp and mutants that do not cause disease. The amplicons for pirA, pirB, 18S rRNA and 16S rRNA showed easily distinguishable melting temperatures of 78.21 ± 0.18, 75.20 ± 0.20, 82.28 ± 0.34 and 85.41 ± 0.21 °C respectively. Additionally, a duplex real-time PCR assay was carried out by designing TaqMan probes for the pirA and pirB primers. The diagnostic sensitivity and specificity was compared between the SYBR Green and TaqMan assays. Both assays showed similar sensitivity with a limit of detection being 10 copies for pirA and pirB, and neither assays showed any cross reaction with other known bacterial and viral pathogens in shrimp. The high sensitivity of both assays make them suitable for the detection of low copies of the pirA and pirB genes in AHPND causing Vibrio spp. as well as for detecting non-pathogenic mutants.
急性肝胰腺坏死病(AHPND),也称为早期死亡综合征(EMS),是一种最近出现的致命疾病,已给虾类养殖业造成重大经济损失。病原体为携带 Photorhabdus Insect-Related (Pir) 毒素基因 pirA 和 pirB 的弧菌属。本研究开发了一种多重 SYBR Green 实时 PCR 方法,可在单个反应中检测 pirA、pirB 和两个内参基因,即虾 18S rRNA 和细菌 16S rRNA 基因。pirB 引物扩增 pirB 基因的 3'-末端,可检测到含有 pirA 完全缺失和 pirB 部分缺失的弧菌属突变体。该检测还可检测到含有完整 pirA 基因和 pirB 基因缺失的突变体。由于这两个毒素基因都是疾病发展所必需的,因此该检测方法可区分引起虾类 AHPND 的致病弧菌属菌株和不致病的突变体。pirA、pirB、18S rRNA 和 16S rRNA 的扩增子显示出易于区分的熔点,分别为 78.21 ± 0.18°C、75.20 ± 0.20°C、82.28 ± 0.34°C 和 85.41 ± 0.21°C。此外,通过设计 pirA 和 pirB 引物的 TaqMan 探针进行了双重实时 PCR 检测。比较了 SYBR Green 和 TaqMan 检测方法的诊断灵敏度和特异性。两种检测方法的灵敏度相似,pirA 和 pirB 的检测限均为 10 拷贝,两种检测方法均与虾类中其他已知细菌和病毒病原体无交叉反应。两种检测方法的高灵敏度均使其适用于检测引起 AHPND 的致病弧菌属中 pirA 和 pirB 基因的低拷贝数,以及检测非致病性突变体。