Han Jee Eun, Tang Kathy F J, Tran Loc H, Lightner Donald V
School of Animal and Comparative Biomedical Sciences, University of Arizona, Tucson, AZ 85721, USA.
Dis Aquat Organ. 2015 Feb 10;113(1):33-40. doi: 10.3354/dao02830.
The 69 kb plasmid pVPA3-1 was identified in Vibrio parahaemolyticus strain 13‑028/A3 that can cause acute hepatopancreatic necrosis disease (AHPND). This disease is responsible for mass mortalities in farmed penaeid shrimp and is referred to as early mortality syndrome (EMS). The plasmid has a GC content of 45.9% with a copy number of 37 per bacterial cell as determined by comparative quantitative PCR analyses. It consists of 92 open reading frames that encode mobilization proteins, replication enzymes, transposases, virulence-associated proteins, and proteins similar to Photorhabdus insect-related (Pir) toxins. In V. parahaemolyticus, these Pir toxin-like proteins are encoded by 2 genes (pirA- and pirB-like) located within a 3.5 kb fragment flanked with inverted repeats of a transposase-coding sequence (1 kb). The GC content of these 2 genes is only 38.2%, substantially lower than that of the rest of the plasmid, which suggests that these genes were recently acquired. Based on a proteomic analysis, the pirA-like (336 bp) and pirB-like (1317 bp) genes encode for 13 and 50 kDa proteins, respectively. In laboratory cultures of V. parahaemolyticus 13-028/A3, both proteins were secreted into the culture medium. We developed a duplex PCR diagnostic method, with a detection limit of 10(5) CFU ml(-1) and targeting pirA- and pirB-like genes in this strain of V. parahaemolyticus. This PCR protocol can reliably detect AHPND-causing strains of V. parahaemolyticus and does not cross react with non-pathogenic strains or with other species of Vibrio isolated from shrimp ponds.
在可导致急性肝胰腺坏死病(AHPND)的副溶血性弧菌菌株13 - 028/A3中鉴定出了69 kb的质粒pVPA3 - 1。这种疾病导致养殖对虾大量死亡,被称为早期死亡综合征(EMS)。通过比较定量PCR分析确定,该质粒的GC含量为45.9%,每个细菌细胞中的拷贝数为37。它由92个开放阅读框组成,这些开放阅读框编码移动蛋白、复制酶、转座酶、毒力相关蛋白以及与发光杆菌昆虫相关(Pir)毒素相似的蛋白。在副溶血性弧菌中,这些类Pir毒素蛋白由位于一个3.5 kb片段内的2个基因(pirA - 和pirB - 样)编码,该片段两侧为转座酶编码序列(1 kb)的反向重复序列。这2个基因的GC含量仅为38.2%,显著低于质粒的其余部分,这表明这些基因是最近获得的。基于蛋白质组学分析,pirA - 样(336 bp)和pirB - 样(1317 bp)基因分别编码13 kDa和50 kDa的蛋白。在副溶血性弧菌13 - 028/A³的实验室培养物中,这两种蛋白都分泌到了培养基中。我们开发了一种双重PCR诊断方法,检测限为10⁵ CFU ml⁻¹,靶向该副溶血性弧菌菌株中的pirA - 和pirB - 样基因。这种PCR方案能够可靠地检测出导致AHPND的副溶血性弧菌菌株,并且不会与非致病菌株或从虾塘分离出的其他弧菌物种发生交叉反应。