Pluta Aneta, Rola-Łuszczak Marzena, Kubiś Piotr, Balov Svetlana, Moskalik Roman, Choudhury Bhudipa, Kuźmak Jacek
OIE Reference Laboratory for EBL, Department of Biochemistry, National Veterinary Research Institute, Pulawy, Poland.
Republican Center for Veterinary Diagnostic, Chisinau, Moldova.
Arch Virol. 2017 Jun;162(6):1563-1576. doi: 10.1007/s00705-017-3241-4. Epub 2017 Feb 17.
Bovine leukemia virus (BLV) is the causative agent of enzootic bovine leukosis (EBL), a disease that has worldwide distribution. Whilst it has been eradicated in most of Western Europe and Scandinavia, it remains a problem in other regions, particularly Eastern Europe and South America. For this study, in 2013, 24 cattle from three farms in three regions of Moldova were screened by ELISA and nested PCR. Of these cattle, 14 which were PCR positive, and these were molecularly characterized based on the nucleotide sequence of the env gene and the deduced amino acid sequence of the encoded gp51 protein. Our results demonstrated a low level of genetic variability (0-2.9%) among BLV field strains from Moldova, in contrast to that observed for other retroviruses, including human immunodeficiency virus (HIV) (20-38%) Mason IL (Trudy vologod moloch Inst 146-164, 1970) and equine infectious anemia virus (EIAV) (~40%) Willems L et al (AIDS Res Hum Retroviruses 16(16):1787-1795, 2000), where the envelope gene exhibits high levels of variation Polat M et al (Retrovirology 13(1):4, 2016). Sequence comparisons and phylogenetic analysis revealed that BLV genotype 7 (G7) is predominant in Moldova and that the BLV population in Moldovan cattle is a mixture of at least three new sub-genotypes: G7D, G7E and G4C. Neutrality tests revealed that negative selection was the major force operating upon the 51-kDa BLV envelope surface glycoprotein subunit gp51, although one positively selected site within conformational epitope G was detected in the N-terminal part of gp51. Furthermore, two functional domains, linear epitope B and the zinc-binding domain, were found to have an elevated ratio of nonsynonymous to synonymous codon differences. Together, these data suggest that the evolutionary constraints on epitopes G and B and the zinc-binding domains of gp51 differ from those on the other domains, with a tendency towards formation of homogenous genetic groups, which is a common concept of global BLV diversification during virus transmission that may be associated with genetic drift.
牛白血病病毒(BLV)是地方流行性牛白血病(EBL)的病原体,这种疾病在全球范围内都有分布。虽然它在西欧大部分地区和斯堪的纳维亚半岛已被根除,但在其他地区,特别是东欧和南美,它仍然是一个问题。在本研究中,2013年,对摩尔多瓦三个地区三个农场的24头牛进行了ELISA和巢式PCR检测。在这些牛中,14头PCR呈阳性,并根据env基因的核苷酸序列和编码的gp51蛋白推导的氨基酸序列进行了分子特征分析。我们的结果表明,摩尔多瓦的BLV田间毒株之间的遗传变异性较低(0-2.9%),这与其他逆转录病毒,包括人类免疫缺陷病毒(HIV)(20-38%)[梅森·伊尔(《沃洛格达乳品研究所学报》第146 - 164页,1970年)]和马传染性贫血病毒(EIAV)(约40%)[威廉姆斯·L等人(《艾滋病研究与人类逆转录病毒》16(16):1787 - 1795,2000年)]形成对比,在这些病毒中,包膜基因表现出高水平的变异[波拉特·M等人(《逆转录病毒学》13(1):4,2016年)]。序列比较和系统发育分析表明,BLV基因型7(G7)在摩尔多瓦占主导地位,并且摩尔多瓦牛群中的BLV群体是至少三种新的亚基因型的混合体:G7D、G7E和G4C。中性检验表明,负选择是作用于51 kDa BLV包膜表面糖蛋白亚基gp51的主要力量,尽管在gp51的N端部分的构象表位G内检测到一个正选择位点。此外,发现两个功能域,线性表位B和锌结合域,非同义密码子与同义密码子差异的比率有所升高。总之,这些数据表明,对gp51的表位G和B以及锌结合域的进化限制与对其他域的限制不同,具有形成同质遗传群体的趋势,这是病毒传播过程中全球BLV多样化的一个常见概念,可能与基因漂变有关。