Huang Yi-wei, Dong Li-bo, Li Jun-hua, Liu Yun-zhi, Gao Li-dong, Zhang Hong, Chen Zhang, Hu Shi-xiong, Li Fang-cai, Shu Yue-long
Hunan Provincial Center for Disease Control and Prevention, Changsha 410005, China.
Zhonghua Liu Xing Bing Xue Za Zhi. 2011 Jul;32(7):709-15.
To understand the possible origins, genetic re-assortment and molecular characterization of 4 highly pathogenic avian influenza A (H5N1) viruses isolated from humans in Hunan province, between 2006 and 2009.
H5N1 PCR test-positive specimens were inoculated in embryonated eggs while H5N1 virus was isolated and genomes sequenced. Genome homology and genetic molecular characterization were analyzed by BLAST and MEGA 4.0.
All gene segments of the 4 viruses were avian in origin. No re-assortment was found between avian influenza A (H5N1) viruses and human seasonal influenza viruses. Viruses that isolated from domestic poultry shared high similarity with the 4 human viruses in gene homology. Data from the whole genome phylogenetic analysis showed that the 4 viruses were in clade 2.3.4, while 2 viruses belonged to genotype V, and another 2 were new genotypes. Results from molecular characterization showed that amino acid sequences of HA cleavage site of the 4 viruses were PLRERRKR/G. All 4 viruses had A160T mutation in HA, a 20 amino acid deletion in the neuraminidase (NA) stalk at position 49 - 68, and a 5 amino acid deletion in the non-structural protein 1 (NS1). Most sites in the HA molecules showed that the viruses preferentially bound to avian influenza virus receptor. However, T192I mutation that might enhance the α 2, 6-linked sialic acid human influenza receptor binding had emerged in HN/1/09 and HN/2/09. D701N mutation of PB2 that increased the virulence in mice was found in HN/1/08. Analysis on drug resistance gene amino acid showed that all 4 viruses were sensitive to amantadine and oseltamivir.
Highly pathogenic avian influenza A (H5N1) viruses isolated from humans in Hunan province from 2006 to 2009 were avian in origin, and the 4 viruses belonged to different genotypes. Some mutations that related to virulence and receptor binding positions had emerged in some of the strains.
了解2006年至2009年从湖南省人类分离出的4株高致病性甲型禽流感(H5N1)病毒的可能来源、基因重配及分子特征。
将H5N1 PCR检测阳性标本接种于鸡胚,分离H5N1病毒并进行基因组测序。采用BLAST和MEGA 4.0软件分析基因组同源性和遗传分子特征。
4株病毒的所有基因片段均来源于禽类。未发现甲型禽流感(H5N1)病毒与人类季节性流感病毒之间发生重配。从家禽中分离出的病毒与4株人类病毒在基因同源性上具有高度相似性。全基因组系统发育分析数据显示,4株病毒属于2.3.4分支,其中2株属于基因型V,另外2株为新基因型。分子特征分析结果显示,4株病毒HA裂解位点的氨基酸序列为PLRERRKR/G。4株病毒HA均有A160T突变,神经氨酸酶(NA)柄部49 - 68位有20个氨基酸缺失,非结构蛋白1(NS1)有5个氨基酸缺失。HA分子中的大多数位点显示,这些病毒优先结合禽流感病毒受体。然而,HN/1/09和HN/2/09中出现了可能增强α2,6 - 连接唾液酸人类流感受体结合的T192I突变。在HN/1/08中发现了增加小鼠毒力的PB2的D701N突变。耐药基因氨基酸分析显示,4株病毒对金刚烷胺和奥司他韦均敏感。
2006年至2009年从湖南省人类分离出的高致病性甲型禽流感(H5N1)病毒来源于禽类,且4株病毒属于不同基因型。部分毒株出现了一些与毒力和受体结合位点相关的突变。