Ferreira Helena Lage, Spilki Fernando Rosado, de Almeida Renata Servan, Santos Márcia M A B, Arns Clarice Weis
Laboratório de Virologia Animal, Departamento de Microbiologia e Imunologia, IB/UNICAMP, PO Box 6109, Campinas CEP: 13083970, SP, Brazil.
Antiviral Res. 2007 Apr;74(1):77-81. doi: 10.1016/j.antiviral.2006.12.002. Epub 2007 Jan 2.
Avian metapneumovirus (AMPV) is the primary causative agent of severe rhinotracheitis in turkeys. It is associated with swollen head syndrome in chickens and is the source of significant economic losses to animal food production. In this study, we designed specific short interfering RNA (siRNA) targeting the AMPV nucleoprotein (N) and fusion (F) genes. Three days post-virus infection, virus titration, real time RT-PCR, and RT-PCR assays were performed to verify the effect of siRNA in AMPV replication. A marked decrease in virus titers from transfected CER cells treated with siRNA/N was observed. Also, the production of N, F, and G mRNAs in AMPV was decreased. Results indicate that N-specific siRNA can inhibit virus replication. In future studies, a combination of siRNAs targeting the RNA polymerase complex may be used as a tool to study AMPV replication and/or antiviral therapy.
禽偏肺病毒(AMPV)是火鸡严重鼻气管炎的主要病原体。它与鸡的肿头综合征有关,是动物食品生产中重大经济损失的来源。在本研究中,我们设计了靶向AMPV核蛋白(N)和融合蛋白(F)基因的特异性小干扰RNA(siRNA)。病毒感染三天后,进行病毒滴定、实时RT-PCR和RT-PCR检测,以验证siRNA对AMPV复制的影响。在用siRNA/N处理的转染CER细胞中观察到病毒滴度显著降低。此外,AMPV中N、F和G mRNA的产生也减少了。结果表明,N特异性siRNA可抑制病毒复制。在未来的研究中,靶向RNA聚合酶复合物的siRNAs组合可作为研究AMPV复制和/或抗病毒治疗的工具。