Sánchez C M, Gebauer F, Suñé C, Mendez A, Dopazo J, Enjuanes L
Centro Nacional de Biotecnología, CSIC-UAM, Universidad Autónoma de Madrid, Spain.
Virology. 1992 Sep;190(1):92-105. doi: 10.1016/0042-6822(92)91195-z.
Transmissible gastroenteritis virus (TGEV) is an enteropathogenic coronavirus isolated for the first time in 1946. Nonenteropathogenic porcine respiratory coronaviruses (PRCVs) have been derived from TGEV. The genetic relationship among six European PRCVs and five coronaviruses of the TGEV antigenic cluster has been determined based on their RNA sequences. The S protein of six PRCVs have an identical deletion of 224 amino acids starting at position 21. The deleted area includes the antigenic sites C and B of TGEV S glycoprotein. Interestingly, two viruses (NEB72 and TOY56) with respiratory tropism have S proteins with a size similar to the enteric viruses. NEB72 and TOY56 viruses have in the S protein 2 and 15 specific amino acid differences with the enteric viruses. Four of the residues changed (aa 219 of NEB72 isolate and aa 92, 94, and 218 of TOY56) are located within the deletion present in the PRCVs and may be involved in the receptor binding site (RBS) conferring enteric tropism to TGEVs. A second RBS used by the virus to infect ST cells might be located in a conserved area between sites A and D of the S glycoprotein, since monoclonal antibodies specific for these sites inhibit the binding of the virus to ST cells. An evolutionary tree relating 13 enteric and respiratory isolates has been proposed. According to this tree, a main virus lineage evolved from a recent progenitor virus which was circulating around 1941. From this, secondary lineages originated PUR46, NEB72, TOY56, MIL65, BR170, and the PRCVs, in this order. Least squares estimation of the origin of TGEV-related coronaviruses showed a significant constancy in the fixation of mutations with time, that is, the existence of a well-defined molecular clock. A mutation fixation rate of 7 +/- 2 x 10(-4) nucleotide substitutions per site and per year was calculated for TGEV-related viruses. This rate falls in the range reported for other RNA viruses. Point mutations and probably recombination events have occurred during TGEV evolution.
传染性胃肠炎病毒(TGEV)是1946年首次分离出的一种肠道致病性冠状病毒。非肠道致病性猪呼吸道冠状病毒(PRCV)由TGEV衍生而来。基于六种欧洲PRCV和TGEV抗原簇的五种冠状病毒的RNA序列,确定了它们之间的遗传关系。六种PRCV的S蛋白在第21位开始有224个氨基酸的相同缺失。缺失区域包括TGEV S糖蛋白的抗原位点C和B。有趣的是,两种具有呼吸道嗜性的病毒(NEB72和TOY56)的S蛋白大小与肠道病毒相似。NEB72和TOY56病毒的S蛋白与肠道病毒分别有2个和15个特定氨基酸差异。其中四个发生变化的残基(NEB72分离株的第219位氨基酸以及TOY56的第92、94和218位氨基酸)位于PRCVs中的缺失区域内,可能参与赋予TGEV肠道嗜性的受体结合位点(RBS)。病毒用于感染ST细胞的第二个RBS可能位于S糖蛋白位点A和D之间的保守区域,因为针对这些位点的单克隆抗体可抑制病毒与ST细胞的结合。已提出了一个涉及13种肠道和呼吸道分离株的进化树。根据这棵树,一个主要病毒谱系从一种1941年左右传播的近期祖病毒进化而来。由此,依次产生了次级谱系PUR46、NEB72、TOY56、MIL65、BR170和PRCVs。对TGEV相关冠状病毒起源的最小二乘估计表明,随着时间的推移,突变固定具有显著的稳定性,即存在明确的分子钟。计算出TGEV相关病毒的每个位点每年的突变固定率为7±2×10⁻⁴个核苷酸替换。该速率落在其他RNA病毒报道的范围内。在TGEV进化过程中发生了点突变以及可能的重组事件。