Chang Sun-Hwa, Bae Jong-Lye, Kang Tae-Jin, Kim Ju, Chung Gook-Hyun, Lim Chae-Woong, Laude Hubert, Yang Moon-Sik, Jang Yong-Suk
Division of Biological Sciences and Institute for Molecular Biology and Genetics, Chonbuk National University, Jeonju, Korea.
Mol Cells. 2002 Oct 31;14(2):295-9.
In order to identify the neutralizing epitope of the porcine epidemic diarrhea virus (PEDV), the spike protein region that is presumed to contain the virus-neutralizing epitope was determined. This was based on the sequence information for the neutralizing epitope of the transmissible gastroenteritis virus (TGEV). A recombinant protein that corresponds to the spike region of TGEV was produced, and polyclonal antisera were generated using the recombinant protein. It was discovered that polyclonal antisera significantly inhibited plaque formation by PEDV, suggesting that this region of the spike protein contains the epitope(s) that is capable of inducing PEDV-neutralizing antibodies. In addition, the region that corresponds to the neutralizing epitope of TGEV may also be involved in neutralizing PEDV, although the two viruses are serologically quite distinct. Finally, the amino acid sequences that are deduced from the genes for the determined-neutralizing epitope were highly homologous among the PEDV strains that were isolated from different geographical areas, which suggests conservation of the antigen gene.
为了鉴定猪流行性腹泻病毒(PEDV)的中和表位,根据传染性胃肠炎病毒(TGEV)中和表位的序列信息,确定了推测含有病毒中和表位的刺突蛋白区域。制备了与TGEV刺突区域相对应的重组蛋白,并使用该重组蛋白产生了多克隆抗血清。发现多克隆抗血清能显著抑制PEDV的蚀斑形成,表明刺突蛋白的该区域含有能够诱导PEDV中和抗体的表位。此外,尽管这两种病毒在血清学上有很大差异,但与TGEV中和表位相对应的区域也可能参与中和PEDV。最后,从不同地理区域分离的PEDV毒株中,由确定的中和表位基因推导的氨基酸序列高度同源,这表明抗原基因具有保守性。