Gyles C L, De Grandis S A, MacKenzie C, Brunton J L
Department of Veterinary Microbiology and Immunology, University of Guelph, Ontario, Canada.
Microb Pathog. 1988 Dec;5(6):419-26. doi: 10.1016/0882-4010(88)90003-4.
The structural genes determining the edema disease principle were cloned from the total cellular DNA of Escherichia coli strain 412 (O139:K82) isolated from a case of porcine edema disease. An assay for cytotoxicity in Vero cells was used to detect the edema disease principle. A 7.5 kb EcoRI-SalI fragment specifying cytotoxin production was subcloned in pUC18. Sequences which specified production of cytotoxin were localized to a 0.9 kb region by transposon Tn5 mutagenesis. A 2.4 kb EcoRI-BglII fragment encompassing this region was subcloned into pUC18. Using nucleotide sequence analysis, two open reading frames separated by 12 bp were identified. They encoded proteins of 319 (A subunit) and 87 (B subunit) amino acids which both had N-terminal sequences typical of E. coli signal peptides. Comparison of these with the published sequence for the Shiga-like toxin II (SLT-II) showed 91% overall nucleotide sequence similarity. The nucleotide sequence similarity extended to 200 base pairs upstream of the putative A subunit translational start site suggesting a common regulatory mechanism. The deduced amino acid sequences of the processed A and B subunits had 94% and 84% similarity, respectively. These findings confirm the close genetic relationship between SLT-II and edema disease principle.
从一例猪水肿病病例分离出的大肠杆菌412株(O139:K82)的总细胞DNA中克隆出决定水肿病致病因子的结构基因。采用在非洲绿猴肾细胞中检测细胞毒性的方法来检测水肿病致病因子。将一个指定产生细胞毒素的7.5 kb EcoRI-SalI片段亚克隆到pUC18中。通过转座子Tn5诱变,将指定产生细胞毒素的序列定位到一个0.9 kb的区域。将包含该区域的一个2.4 kb EcoRI-BglII片段亚克隆到pUC18中。利用核苷酸序列分析,鉴定出两个被12 bp隔开的开放阅读框。它们编码319个氨基酸(A亚基)和87个氨基酸(B亚基)的蛋白质,二者均具有典型的大肠杆菌信号肽N端序列。将这些序列与志贺样毒素II(SLT-II)的已发表序列进行比较,结果显示总体核苷酸序列相似性为91%。核苷酸序列相似性延伸至假定的A亚基翻译起始位点上游200个碱基对处,提示存在共同的调控机制。推导的加工后A亚基和B亚基的氨基酸序列相似性分别为94%和84%。这些发现证实了SLT-II与水肿病致病因子之间密切的遗传关系。