Department of Entomology, Pennsylvania State University, University Park, PA, USA.
Center for Infectious Disease Dynamics, Pennsylvania State University, University Park, PA, USA.
J Gen Virol. 2024 Aug;105(8). doi: 10.1099/jgv.0.002017.
West Nile virus (WNV) is the leading cause of mosquito-borne illness in the USA. There are currently no human vaccines or therapies available for WNV, and vector control is the primary strategy used to control WNV transmission. The WNV vector is also a competent host for the insect-specific virus (ISV) Eilat virus (EILV). ISVs such as EILV can interact with and cause superinfection exclusion (SIE) against human pathogenic viruses in their shared mosquito host, altering vector competence for these pathogenic viruses. The ability to cause SIE and their host restriction make ISVs a potentially safe tool to target mosquito-borne pathogenic viruses. In the present study, we tested whether EILV causes SIE against WNV in mosquito C6/36 cells and mosquitoes. The titres of both WNV strains - WN02-1956 and NY99 - were suppressed by EILV in C6/36 cells as early as 48-72 h post-superinfection at both m.o.i. values tested in our study. The titres of WN02-1956 at both m.o.i. values remained suppressed in C6/36 cells, whereas those of NY99 showed some recovery towards the final timepoint. The mechanism of SIE remains unknown, but EILV was found to interfere with NY99 attachment in C6/36 cells, potentially contributing to the suppression of NY99 titres. However, EILV had no effect on the attachment of WN02-1956 or internalization of either WNV strain under superinfection conditions. In , EILV did not affect the infection rate of either WNV strain at either timepoint. However, in mosquitoes EILV enhanced NY99 infection titres at 3 days post-superinfection, but this effect disappeared at 7 days post-superinfection. In contrast, WN02-1956 infection titres were suppressed by EILV at 7 days post-superinfection. The dissemination and transmission of both WNV strains were not affected by superinfection with EILV at either timepoint. Overall, EILV caused SIE against both WNV strains in C6/36 cells; however, in , SIE caused by EILV was strain specific potentially owing to differences in the rate of depletion of shared resources by the individual WNV strains.
西尼罗河病毒(WNV)是美国主要的蚊媒疾病病原体。目前尚无针对 WNV 的人体疫苗或疗法,而病媒控制是控制 WNV 传播的主要策略。WNV 的载体也是昆虫特异性病毒(ISV)伊拉特病毒(EILV)的有效宿主。EILV 等 ISV 可以与蚊媒中的人类致病病毒相互作用并引起超感染排斥(SIE),从而改变这些致病病毒的媒介效能。EILV 能够引起 SIE 及其宿主限制使其成为针对蚊媒传播的致病病毒的潜在安全工具。在本研究中,我们测试了 EILV 是否会在蚊细胞 C6/36 和蚊子中引起对 WNV 的 SIE。在我们研究的两种 m.o.i. 值下,EILV 早在感染后 48-72 小时就抑制了两种 WNV 株-WN02-1956 和 NY99-在 C6/36 细胞中的病毒滴度。在两种 m.o.i. 值下,WN02-1956 的病毒滴度在 C6/36 细胞中仍受到抑制,而 NY99 的病毒滴度在最终时间点有所恢复。SIE 的机制尚不清楚,但发现 EILV 干扰了 C6/36 细胞中 NY99 的附着,这可能导致 NY99 病毒滴度的抑制。然而,EILV 对 WN02-1956 的附着或两种 WNV 株在超感染条件下的内化没有影响。在 ,EILV 对两种 WNV 株在任何时间点的感染率均无影响。然而,在蚊子中,EILV 在感染后 3 天增强了 NY99 的感染滴度,但这种作用在感染后 7 天消失。相比之下,EILV 在感染后 7 天抑制了 WN02-1956 的感染滴度。在任何时间点,EILV 对两种 WNV 株的传播和传播均无影响。总体而言,EILV 在 C6/36 细胞中引起了对两种 WNV 株的 SIE;然而,在 ,EILV 引起的 SIE 是株特异性的,这可能是由于两种 WNV 株对共享资源的消耗速度不同所致。