Son E S, Ahn H J, Kim J H, Kim D Y, Nam H W
Department of Parasitology, Catholic Institute of Parasitic Diseases, Catholic University of Korea.
Korean J Parasitol. 2001 Sep;39(3):241-6. doi: 10.3347/kjp.2001.39.3.241.
The antigenic domain of the major surface protein (Nc-p43) of Neospora caninum was examined by polymerase chain reaction of its gene fragments and recombinant expression as GST fusion proteins. The fragments of Nc-p43 were as follow: a total open reading frame (OFR), T; OFR without signal sequence and C-terminal hydrophobic sequence, S; N-terminal 2/3 parts of S, A; C-terminal 2/3 parts, P; N-terminal 1/3 part, X; middle 1/3 part, Y; and C-terminal 1/3 part, Z, respectively. The DNA fragments were cloned into pGEX-4T vector. Recombinant plasmids transformed into Escherichia coli of BL21 pLysS (DE3) strain were induced to express GST or GST fused fragments of Nc-p43 such as 69 kDa protein for T, 66 kDa for S, 52 kDa for A, 53 kDa for P, and 40 kDa proteins for X, Y, and Z, respectively in SDS-PAGE. The Nc-p43 fragments of T, S, and P reacted with a bovine serum of neosporosis while those of A, X, Y, and Z together with GST did not in the western blot. These findings suggest that the antigenic domain of Nc-p43 of N. caninum may be localized in the C-terminal 2/3 parts. Together with A19 clone in SAG1 of Toxoplasma gondii (Nam et al., 1996), the P fragment of Nc-p43 could be used as efficient antigens to diagnose and differentiate those infections with both species.
通过对犬新孢子虫主要表面蛋白(Nc-p43)基因片段进行聚合酶链反应并将其作为谷胱甘肽S-转移酶(GST)融合蛋白进行重组表达,对该蛋白的抗原结构域进行了研究。Nc-p43的片段如下:一个完整的开放阅读框(OFR),记为T;不含信号序列和C端疏水序列的OFR,记为S;S的N端2/3部分,记为A;C端2/3部分,记为P;N端1/3部分,记为X;中间1/3部分,记为Y;以及C端1/3部分,记为Z。将DNA片段克隆到pGEX-4T载体中。将重组质粒转化到BL21 pLysS(DE3)菌株的大肠杆菌中,诱导表达GST或GST融合的Nc-p43片段,如在SDS-PAGE中,T片段表达的69 kDa蛋白、S片段表达的66 kDa蛋白、A片段表达的52 kDa蛋白、P片段表达的53 kDa蛋白以及X、Y和Z片段表达的40 kDa蛋白。在蛋白质免疫印迹中,T、S和P的Nc-p43片段与牛新孢子虫病血清发生反应,而A、X、Y和Z片段以及GST则未发生反应。这些结果表明,犬新孢子虫Nc-p43的抗原结构域可能位于C端2/3部分。与刚地弓形虫SAG1中的A19克隆(Nam等人,1996年)一起,Nc-p43的P片段可作为高效抗原用于诊断和区分这两种寄生虫的感染。