Suppression of the induction of alpha, beta, and gamma interferons by the NS1 and NS2 proteins of human respiratory syncytial virus in human epithelial cells and macrophages

被引:338
作者
Spann, KM
Tran, KC
Chi, B
Rabin, RL
Collins, PL
机构
[1] NIAID, Infect Dis Lab, NIH, Bethesda, MD 20892 USA
[2] Ctr Biol Evaluat & Res, Food & Drug Adm, Lab Immunobiochem, Bethesda, MD 20892 USA
关键词
D O I
10.1128/JVI.78.8.4363-4369.2004
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Wild-type human respiratory syncytial virus (HRSV) is a poor inducer of alpha/beta interferons (IFN-alpha/beta). However, recombinant HRSV lacking the NS1 and NS2 genes (DeltaNSI/2) induced high levels of IFN-alpha and -beta in human pulmonary epithelial cells (A549) as well as in macrophages derived from primary human peripheral blood monocytes. Results with NS1 and NS2 single- and double-gene-deletion viruses indicated that the two proteins function independently as well as coordinately to achieve the full inhibitory effect, with NS1 having a greater independent role. The relative contributions of the individual NS proteins were the converse of that recently described for bovine RSV (J. F. Valarcher, J. Furze, S. Wyld, R. Cook, K. K. Conzelmann, and G. Taylor, J. Virol. 77:8426-8439, 2003). This pattern of inhibition by HRSV NS1 and NS2 also extended to the newly described antiviral cytokines IFN-lambda1, -2 and -3.
引用
收藏
页码:4363 / 4369
页数:7
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