Gebauer F, de la Torre J C, Gomes I, Mateu M G, Barahona H, Tiraboschi B, Bergmann I, de Mello P A, Domingo E
Centro de Biología Molecular, Universidad Autónoma de Madrid, Spain.
J Virol. 1988 Jun;62(6):2041-9. doi: 10.1128/JVI.62.6.2041-2049.1988.
Rapid evolution of foot-and-mouth disease virus (FMDV) is documented during persistent infections of cattle. The carrier state was established experimentally with plaque-purified FMDV of serotype C3. Virus was recovered from the esophageal pharyngeal area of the animals up to 539 days postinfection. Analysis of capsid proteins by electrofocusing and by electrophoretic mobility of the genomic poly(C)-rich tract suggested heterogeneity in several isolates and sequential dominance of viral subpopulations. Nucleotide sequences of the VP1-coding region of the parental FMDV C3 clones and of seven isolates from the carrier cattle showed point mutations that represented rates of fixation of mutations of 0.9 X 10(-2) to 7.4 X 10(-2) substitutions per nucleotide per year; 59% of the base changes led to amino acid substitutions, some of which were located within residues 135 to 151, a region involved in neutralization of FMDV. In the esophageal pharyngeal fluid samples, FMDV C3-neutralizing activity was present. Antigenic variation was demonstrated with monoclonal antibodies raised against FMDV C3. Two isolates from carrier cattle differed from the parental virus by 10(2)- or 10(3)-fold decreased reactivity with neutralizing monoclonal antibodies. We suggest that persistent, inapparent infections of ruminants, in addition to being a reservoir of virus, may promote the rapid selection of antigenically variant FMDVs.
口蹄疫病毒(FMDV)在牛的持续性感染期间呈现出快速进化。通过用C3血清型的蚀斑纯化FMDV进行实验建立了携带状态。在感染后长达539天的时间里,从动物的食管咽部区域分离到了病毒。通过电聚焦分析衣壳蛋白以及通过基因组富含多聚(C)区域的电泳迁移率分析表明,几个分离株存在异质性,并且病毒亚群呈现出顺序性优势。亲代FMDV C3克隆以及来自携带病毒牛的七个分离株的VP1编码区的核苷酸序列显示出点突变,其代表的突变固定率为每年每核苷酸0.9×10⁻²至7.4×10⁻²个替换;59%的碱基变化导致氨基酸替换,其中一些位于135至151位残基内,该区域参与FMDV的中和作用。在食管咽部液体样本中,存在FMDV C3中和活性。用针对FMDV C3产生的单克隆抗体证明了抗原变异。来自携带病毒牛的两个分离株与亲代病毒相比,与中和单克隆抗体的反应性降低了10²倍或10³倍。我们认为,反刍动物的持续性隐性感染,除了作为病毒的储存库外,可能会促进抗原性变异的FMDV的快速选择。