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首页> 外文期刊>Avian Pathology >Variability of tropism and replicative capacity of two naturally occurring influenza A H9N2 viruses in cell cultures from different tissues
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Variability of tropism and replicative capacity of two naturally occurring influenza A H9N2 viruses in cell cultures from different tissues

机译:不同组织的细胞培养物中两种天然存在的甲型H9N2流感病毒的嗜性变异和复制能力

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摘要

Studies carried out on cell permissivity are of great interest to understand virus replication and pathogenicity. We described the results of a comparative analysis of replication efficiency of two naturally occurring influenza A H9N2 variants isolated from poultry and wild birds, differing by only two substitutions Q226L and T384N, in the receptor-binding site of haemagglutinin and the 380 loop region of NA proteins, respectively. Considering the overall growth of both viruses, lung cultures ensured the most efficient growth of TUN12L226N384 strain with titres up to 10(9) TCID50/ml whereas small intestine culture was highly susceptible to the TUN51Q226T384 virus reaching a titre of 10(6) TCID50/ml. The lowest replication was shown in liver cells. The addition of trypsin was essential for the replication of either virus in primary fibroblasts, but it had a marginal positive effect on virus replication in the four other culture types with maximum titres of 10(8) TCID50/ml. This means that in chicken, the proteolytic activation of the H9N2 viruses with the cleavage motif RSSR may be mediated by other endoproteases than trypsin. Further investigations should concentrate on the production of the appropriate set of viruses by a reverse genetics approach and the examination of cellular protease expression in chicken tissues. This would lead to a more complete understanding of the tropism of low-pathogenic Influenza A viruses.
机译:对细胞介电常数的研究对于了解病毒复制和致病性非常重要。我们描述了从家禽和野生鸟类中分离的两种天然存在的甲型流感H9N2变异体的复制效率的比较分析结果,它们在血凝素的受体结合位点和NA的380环区域中仅两个取代Q226L和T384N有所不同蛋白质。考虑到两种病毒的总体生长情况,肺培养物可确保滴定度高达10(9)TCID50 / ml的TUN12L226N384菌株最有效的生长,而小肠培养物对TUN51Q226T384病毒的滴度高达10(6)TCID50 /非常敏感。毫升在肝细胞中显示出最低的复制。胰蛋白酶的添加对于在原代成纤维细胞中复制任何一种病毒都是必不可少的,但是它对其他四种最大滴度为10(8)TCID50 / ml的培养类型中的病毒复制具有微弱的积极影响。这意味着在鸡中,具有裂解基序RSSR的H9N2病毒的蛋白水解激活可能是由胰蛋白酶以外的其他内切蛋白酶介导的。进一步的研究应集中在通过逆向遗传学方法生产适当的一组病毒以及检查鸡组织中细胞蛋白酶的表达。这将导致人们对低致病性甲型流感病毒的嗜性有更全面的了解。

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