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Attenuated Foot-and-Mouth Disease Virus RNA Carrying a Deletion in the 3′ Noncoding Region Can Elicit Immunity in Swine

机译:在3'非编码区中缺​​失的减毒口蹄疫病毒RNA可以激发猪的免疫力

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摘要

We constructed foot-and-mouth disease virus (FMDV) mutants bearing independent deletions of the two stem-loop structures predicted in the 3′ noncoding region of viral RNA, SL1 and SL2, respectively. Deletion of SL2 was lethal for viral infectivity in cultured cells, while deletion of SL1 resulted in viruses with slower growth kinetics and downregulated replication associated with impaired negative-strand RNA synthesis. With the aim of exploring the potential of an RNA-based vaccine against foot-and-mouth disease using attenuated viral genomes, full-length chimeric O1K/C-S8 RNAs were first inoculated into pigs. Our results show that FMDV viral transcripts could generate infectious virus and induce disease in swine. In contrast, RNAs carrying the ΔSL1 mutation on an FMDV O1K genome were innocuous for pigs but elicited a specific immune response including both humoral and cellular responses. A single inoculation with 500 μg of RNA was able to induce a neutralizing antibody response. This response could be further boosted by a second RNA injection. The presence of the ΔSL1 mutation was confirmed in viruses isolated from serum samples of RNA-inoculated pigs or after transfection and five passages in cell culture. These findings suggest that deletion of SL1 might contribute to FMDV attenuation in swine and support the potential of RNA technology for the design of new FMDV vaccines.
机译:我们构建了口蹄疫病毒(FMDV)突变体,分别携带两个分别在病毒RNA 3'非编码区SL1和SL2的非编码区中预测的茎环结构的缺失。 SL2的缺失对培养细胞的病毒感染性具有致命性,而SL1的缺失导致病毒的生长动力学较慢,并且复制受到抑制,负链RNA合成受损。为了探索使用减毒病毒基因组的针对口蹄疫的基于RNA的疫苗的潜力,首先将全长嵌合O1K / C-S8 RNA接种到猪中。我们的结果表明,FMDV病毒转录本可以产生感染性病毒并诱发猪的疾病。相比之下,在FMDV O1K基因组上携带ΔSL1突变的RNA对猪无害,但引起了特异性免疫反应,包括体液和细胞反应。一次接种500μgRNA能够诱导中和抗体反应。再次注射RNA可进一步增强这种反应。 ΔSL1突变的存在已在从RNA感染的猪血清样本中分离的病毒中或转染后和在细胞培养中传代5次后确认。这些发现表明,SL1的缺失可能导致猪FMDV减毒,并支持RNA技术在设计新FMDV疫苗方面的潜力。

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