College of Veterinary Medicine, South China Agricultural University, Guangzhou 510642, China.
Guangdong Inspection and Quarantine Technology Center, Guangzhou 510623, China.
Viruses. 2019 Apr 29;11(5):402. doi: 10.3390/v11050402.
Nucleoprotein (N) is a key element in rabies virus (RABV) replication. To further investigate the effect of N on RABV, we manipulated an infectious cDNA clone of the RABV HEP-Flury to rearrange the N gene from its wild-type position of 1 (N-P-M-G-L) to 2 (P-N-M-G-L), 3 (P-M-N-G-L), or 4 (P-M-G-N-L), using an approach that left the viral nucleotide sequence unaltered. Subsequently, viable viruses were recovered from each of the rearranged cDNA and examined for their gene expression levels, growth kinetics in cell culture, pathogenicity in suckling mice and protection in mice. The results showed that gene rearrangement decreased N mRNA transcription and vRNA replication. As a result, all viruses with rearranged genomes showed worse replication than that of rHEP-Flury in NA cells at a MOI of 0.01, but equivalent or slightly better replication levels at a MOI of 3. Consequently, the lethality in suckling mice infected with N4 was clearly attenuated compared with rHEP-Flury. However, the protection to mice was not enhanced. This study not only gives us insight into the understanding of the phenotype of RABV N gene rearrangement, but also helps with rabies vaccine candidate construction.
核蛋白(N)是狂犬病病毒(RABV)复制的关键元素。为了进一步研究 N 对 RABV 的影响,我们操纵了 RABV HEP-Flury 的传染性 cDNA 克隆,将 N 基因从其野生型位置 1(N-P-M-G-L)重排到 2(P-N-M-G-L)、3(P-M-N-G-L)或 4(P-M-G-N-L),同时保持病毒核苷酸序列不变。随后,从每个重排的 cDNA 中恢复了有活力的病毒,并检查了它们的基因表达水平、在细胞培养中的生长动力学、在乳鼠中的致病性和在小鼠中的保护作用。结果表明,基因重排降低了 N mRNA 转录和 vRNA 复制。因此,所有重排基因组的病毒在 MOI 为 0.01 的情况下,在 NA 细胞中的复制能力均低于 rHEP-Flury,但在 MOI 为 3 的情况下,其复制水平相当或略有提高。因此,与 rHEP-Flury 相比,感染 N4 的乳鼠的致死性明显减弱。然而,对小鼠的保护作用并没有增强。这项研究不仅使我们深入了解了 RABV N 基因重排的表型,还有助于狂犬病疫苗候选物的构建。