Zhu Ru-Nan, Qian Yuan, Zhao Lin-Qing, Sun Yu, Deng Jie, Wang Fang
Laboratory of Virology, Capital Institute of Pediatrics, Beijing 100020, China.
Bing Du Xue Bao. 2011 Nov;27(6):557-64.
Human metapneumovirus (hMPV) is associated with acute respiratory tract infections (ARTI) in all age groups. However, there is limited information of genetic analysis of hMPV circulating in Beijing. To learn the characteristics of structural protein genes of human metapneumovirus circulating in children in Beijing, sequence analysis of matrix (M), small hydrophobic (SH) and attachment (G) proteins of hMPV from 2006 to 2010 was performed. Phylogenetic analysis of nucleotide sequences of 42 full length M genes, 49 SH gene and 55 G gene revealed that the hMPVs from pediatric patients were divided into sub-genotypes A2, B1 and B. There were highly conserved identities among M gene, with 7 conserved mutations of amino acids between A and B genotypes which were fairly conserved in the same genotype A or B. The amino acid identities of SH were 60.7% to 64.4% between different genotypes, 93.3% - 100% among same sub-genotype and 84.7% - 88.7% between different sub-genotypes. Use of alternative transcription-termination codon, nucleotide deletion and insertion resulted in variable length of nucleotide and deduced amino acid of G protein. Amino acid identities within same genotype ranged from 81.5% - 100%, whereas sequence identities between two genotypes ranged from 34.0% - 38.6% at the amino acid level. A new cluster of G genes in sub-genotype B2 appeared due to the same mutations and insertion of two amino acids in G protein encoding genes amplified from specimens collected from 2008 to 2010. Prediction of antigen sites of SH and G protein indicated that the variation of antigen sites between different sub-genotypes existed.
人偏肺病毒(hMPV)与各年龄组的急性呼吸道感染(ARTI)相关。然而,关于在北京流行的hMPV的基因分析信息有限。为了解在北京儿童中流行的人偏肺病毒结构蛋白基因的特征,对2006年至2010年hMPV的基质(M)、小疏水(SH)和附着(G)蛋白进行了序列分析。对42个全长M基因、49个SH基因和55个G基因的核苷酸序列进行系统发育分析,结果显示儿科患者的hMPV分为A2、B1和B亚型。M基因之间存在高度保守的同一性,A和B基因型之间有7个保守的氨基酸突变,在同一A或B基因型中相当保守。不同基因型之间SH的氨基酸同一性为60.7%至64.4%,同一亚型内为93.3% - 100%,不同亚型之间为84.7% - 88.7%。使用替代转录终止密码子、核苷酸缺失和插入导致G蛋白的核苷酸和推导氨基酸长度可变。同一基因型内的氨基酸同一性范围为81.5% - 100%,而两个基因型之间的序列同一性在氨基酸水平上范围为34.0% - 38.6%。由于从2008年至2010年收集的标本中扩增的G蛋白编码基因存在相同突变和两个氨基酸插入,在B2亚型中出现了一个新的G基因簇。SH和G蛋白抗原位点的预测表明不同亚型之间存在抗原位点变异。