Brown A L, Campbell R O, Clarke B E
Department of Virology, Wellcome Biotechnology Ltd., Beckenham, Kent, U.K.
Gene. 1989 Feb 20;75(2):225-33. doi: 10.1016/0378-1119(89)90268-0.
The nucleotide sequence coding for the structural proteins and nonstructural protein P2A has been determined for a foot-and-mouth disease virus (FMDV) isolated in Africa. This virus, serotypically designated SAT3 (South African Territories type 3), shows about 60% homology at the nucleotide level to prototype viruses from the O, A and C serotypes of FMDV. The highest region of variability was shown in structural protein VP1, presumably a consequence of its position on the surface of the virus and its exposure to selection pressure by neutralising antibody. Within this region amino acids (aa) 141-160, which have been shown to represent an immunodominant region in other FMDV serotypes, showed hypervariability as well as the insertion of 5 or 9 additional aa relative to the O1 and C1 serotypes, respectively. In contrast, the sequence of nonstructural protein P2A was completely conserved indicating a probable important role in virus replication.
已确定从非洲分离出的一种口蹄疫病毒(FMDV)编码结构蛋白和非结构蛋白P2A的核苷酸序列。这种病毒血清型定为SAT3(南非3型),在核苷酸水平上与口蹄疫病毒O、A和C血清型的原型病毒显示出约60%的同源性。结构蛋白VP1显示出最高的变异区域,推测这是由于其位于病毒表面的位置以及其受到中和抗体的选择压力所致。在该区域内,已证明在其他口蹄疫病毒血清型中代表免疫显性区域的氨基酸(aa)141 - 160显示出高变异性,并且相对于O1和C1血清型分别插入了5个或9个额外的氨基酸。相比之下,非结构蛋白P2A的序列完全保守,表明其在病毒复制中可能起重要作用。