Key Laboratory of Animal Epidemiology of the Ministry of Agriculture, College of Veterinary Medicine, China Agricultural University, Beijing, China.
Virulence. 2023 Dec;14(1):2186336. doi: 10.1080/21505594.2023.2186336.
We previously demonstrated that two methyltransferase motifs, K-D-K-E and G-G-D, affect the pathogenicity of Newcastle disease virus (NDV) by regulating mRNA translation and virus transmission. Here, we compared the infectious centre area produced by the NDV strain, rSG10, and methyltransferase motifs mutant rSG10 strains in DF-1 cells. The results show that intercellular transmission was attenuated by methyltransferase motif mutations. We further determined the ability of mutant viruses to spread in cell-free and cell-to-cell situations. Cell-free transmission of rSG10-K1756A was not reduced, indicating that cell-to-cell transmission of rSG10-K1756A was decreased. Using a donor and target system, we demonstrated that NDV can spread from cell-to-cell directly. Furthermore, by comparing the protein distribution area of three strains when treated with 2% agar overlay, we found that rSG10-K1756A was defective in cell-to-cell transmission. Tunnelling nanotubes (TNTs) are an important mode for cell-to-cell transmission. Treatment of cells with cytochalasin D (CytoD) or nocodazole to inhibit the formation of TNTs, reduced protein levels in all strains, but rSG10-K1756A was the least affected. These results indicate that mutation of the K-D-K-E motif is likely to restricted the spread of NDV via TNTs. Finally, we observed that matrix protein (M) and fusion protein (F) promoted the formation of cellular extensions, which may be involved in the cell-to-cell spread of NDV. Our research reveals a novel mechanism by which methyltransferase motifs affect the cell-to-cell spread of NDV and provides insight into dissemination of paramyxoviruses.
我们之前的研究表明,两个甲基转移酶基序 K-D-K-E 和 G-G-D 通过调节 mRNA 翻译和病毒传播,影响新城疫病毒(NDV)的致病性。在这里,我们比较了 NDV 株 rSG10 和甲基转移酶基序突变株 rSG10 在 DF-1 细胞中产生的感染中心区域。结果表明,甲基转移酶基序突变削弱了细胞间传播。我们进一步确定了突变病毒在无细胞和细胞间情况下的扩散能力。rSG10-K1756A 的无细胞传播没有减少,表明 rSG10-K1756A 的细胞间传播减少。使用供体和靶系统,我们证明 NDV 可以直接从细胞间传播。此外,通过比较三种菌株在 2%琼脂覆盖物处理下的蛋白分布区域,我们发现 rSG10-K1756A 在细胞间传播中存在缺陷。隧道纳米管(TNTs)是细胞间传播的一种重要方式。用细胞松弛素 D(CytoD)或诺考达唑处理细胞以抑制 TNTs 的形成,降低了所有菌株的蛋白水平,但 rSG10-K1756A 的影响最小。这些结果表明,K-D-K-E 基序的突变可能限制了 NDV 通过 TNTs 的传播。最后,我们观察到基质蛋白(M)和融合蛋白(F)促进了细胞延伸的形成,这可能与 NDV 的细胞间传播有关。我们的研究揭示了甲基转移酶基序影响 NDV 细胞间传播的新机制,并为副粘病毒的传播提供了新的认识。