Fodha I, Vabret A, Bouslama L, Leroux M, Legrand L, Dina J, Gouarin S, Petitjean J, Dewar J, Trabelsi A, Boujaafar N, Freymuth F
Laboratory of bacteriology-virology, university hospital Sahloul, 4000 Sousse, Tunisia.
Pathol Biol (Paris). 2008 Mar;56(2):50-7. doi: 10.1016/j.patbio.2007.06.001. Epub 2007 Oct 4.
Two major antigenic subgroups (designated A and B) have been described for human respiratory syncytial virus (HRSV). Between and within the two main subgroups, there is antigenic variation in the attachment protein G. The variability of the G protein is known to be located in two hypervariable regions of the ectodomain. Most investigators have studied the gene segment coding the C-terminal end of the protein, and little is known about the N-terminal variable region. In the present study, the genetic variability of HRSV subgroup B was evaluated by nucleotide sequencing of the N-terminal region of the G gene of 52 Tunisian isolates. Tunisian subgroup B isolates clustered into two main lineages designated arbitrarily as Tu-GB1 and Tu-GB2. Three distinct subtypes were identified within genotype Tu-GB2. The inter- and intragenotype nucleotide variability ranged from 4 to 8% and from 0 to 4%, respectively. Overall divergence values of the G sequences were inferior or equal to 15% at the aminoacid level. Comparison of sequences among Tunisian HRSV strains and viruses isolated in other geographical areas during different epidemics demonstrated close similarity to strains from Kenya, Belgium, the UK, Qatar, Canada and South Korea.
人类呼吸道合胞病毒(HRSV)已被描述为两个主要的抗原亚组(分别命名为A和B)。在这两个主要亚组之间以及亚组内部,附着蛋白G存在抗原变异。已知G蛋白的变异性位于胞外域的两个高变区。大多数研究人员研究了编码该蛋白C末端的基因片段,而对N末端可变区了解甚少。在本研究中,通过对52株突尼斯分离株G基因N末端区域进行核苷酸测序,评估了HRSV B亚组的遗传变异性。突尼斯B亚组分离株聚为两个主要谱系,分别任意命名为Tu-GB1和Tu-GB2。在基因型Tu-GB2内鉴定出三个不同的亚型。基因型间和基因型内的核苷酸变异性分别为4%至8%和0%至4%。G序列在氨基酸水平的总体差异值小于或等于15%。突尼斯HRSV毒株与在不同疫情期间在其他地理区域分离的病毒之间的序列比较表明,它们与来自肯尼亚、比利时、英国、卡塔尔、加拿大和韩国的毒株非常相似。