Pignatelli S, Dal Monte P, Rossini G, Chou S, Gojobori T, Hanada K, Guo J J, Rawlinson W, Britt W, Mach M, Landini M P
Department of Clinical and Experimental Medicine, Division Microbiology - St Orsola General Hospital, University of Bologna, Via Massarenti 9, 40138 Bologna, Italy.
Medical and Research Services, VA Medical Center and Division of Infectious Diseases, Oregon Health Sciences University, Portland, OR, USA.
J Gen Virol. 2003 Mar;84(Pt 3):647-655. doi: 10.1099/vir.0.18704-0.
Human cytomegalvirus (HCMV) ORF UL73 is a polymorphic locus, encoding the viral glycoprotein gpUL73-gN, a component of the gC-II envelope complex. The previously identified gN genomic variants, denoted gN-1, gN-2, gN-3 and gN-4, were further investigated in this work by analysing a large panel of HCMV clinical isolates collected from all over the world (223 samples). Sequencing and phylogenetic analysis confirmed the existence of the four gN genotypes, but also allowed the identification of a novel subgroup belonging to the gN-3 genotype, which was designated gN-3b. The number of non-synonymous (d(N)) and synonymous (d(S)) nucleotide substitutions and their ratio (d(N)/d(S)) were estimated among the gN genotypes to evaluate the possibility of positive selection. Results showed that the four variants evolved by neutral (random) selection, but that the gN-3 and gN-4 genotypes are maintained by positive selective pressure. The 223 HCMV clinical isolates were subdivided according to their geographical origin, and four main regions of gN prevalence were identified: Europe, China, Australia and Northern America. The gN variants were found to be widespread and represented within the regions analysed without any significant difference, and no new genotype was detected. Finally, for clinical and epidemiological purposes, a rapid and low-cost method for genetic grouping of the HCMV clinical isolates was developed based on the RFLP revealed by SacI, ScaI and SalI digestion of the PCR-amplified UL73 sequence. This technique enabled us to distinguish all four gN genomic variants and also their subtypes.
人巨细胞病毒(HCMV)开放阅读框UL73是一个多态性位点,编码病毒糖蛋白gpUL73-gN,它是gC-II包膜复合物的一个组成部分。在本研究中,通过分析从世界各地收集的大量HCMV临床分离株(223个样本),对先前鉴定的gN基因组变体gN-1、gN-2、gN-3和gN-4进行了进一步研究。测序和系统发育分析证实了四种gN基因型的存在,同时还鉴定出一个属于gN-3基因型的新亚组,命名为gN-3b。估计gN基因型之间非同义(d(N))和同义(d(S))核苷酸替换的数量及其比率(d(N)/d(S)),以评估正选择的可能性。结果表明,这四种变体通过中性(随机)选择进化,但gN-3和gN-4基因型受到正选择压力的维持。根据地理来源对223株HCMV临床分离株进行了细分,确定了gN流行的四个主要地区:欧洲、中国、澳大利亚和北美洲。发现gN变体在分析的区域内广泛存在且无显著差异,未检测到新的基因型。最后,出于临床和流行病学目的,基于PCR扩增的UL73序列经SacI、ScaI和SalI消化后显示的限制性片段长度多态性(RFLP),开发了一种快速、低成本的HCMV临床分离株基因分型方法。该技术使我们能够区分所有四种gN基因组变体及其亚型。