Joseph Renuka E, Bozic Jovana, Werling Kristine L, Urakova Nadya, Rasgon Jason L
Department of Entomology, Pennsylvania State University, University Park, PA, United States.
Center for Infectious Disease Dynamics, Pennsylvania State University, University Park, PA, United States.
bioRxiv. 2023 May 25:2023.05.25.542294. doi: 10.1101/2023.05.25.542294.
West Nile virus (WNV) is the leading cause of mosquito-borne illness in the United States. 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 titers 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 multiplicity of infections (MOIs) tested in our study. The titers of WN02-1956 at both MOIs 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 titers. 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 titers at 3 days post superinfection, but this effect disappeared at 7 days post superinfection. In contrast, WN02-1956 infection titers 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)是美国蚊媒疾病的主要病因。目前尚无针对WNV的人类疫苗或疗法,病媒控制是用于控制WNV传播的主要策略。WNV病媒也是昆虫特异性病毒(ISV)埃拉特病毒(EILV)的适宜宿主。诸如EILV之类的ISV可以在其共同的蚊宿主中与人类致病病毒相互作用并导致超感染排斥(SIE),从而改变这些致病病毒的病媒能力。引起SIE的能力及其宿主限制性使ISV成为靶向蚊媒致病病毒的潜在安全工具。在本研究中,我们测试了EILV在蚊C6/36细胞和蚊子中是否对WNV引起SIE。早在超感染后48 - 72小时,在我们研究测试的两种感染复数(MOI)下,EILV均在C6/36细胞中抑制了两种WNV毒株——WN02 - 1956和NY99的滴度。在C6/36细胞中,两种MOI下WN02 - 1956的滴度均保持被抑制状态,而NY99的滴度在接近最终时间点时有所恢复。SIE的机制仍然未知,但发现EILV在C6/36细胞中干扰了NY99的附着,这可能有助于抑制NY99的滴度。然而,在超感染条件下,EILV对WN02 - 1956的附着或两种WNV毒株的内化均无影响。在[此处原文缺失相关内容]中,EILV在任何时间点均未影响两种WNV毒株的感染率。然而,在蚊子中,EILV在超感染后3天提高了NY99的感染滴度,但这种效果在超感染后7天消失。相反,在超感染后7天,EILV抑制了WN02 - 1956的感染滴度。在任何时间点,EILV的超感染均未影响两种WNV毒株的传播和扩散。总体而言,EILV在C6/36细胞中对两种WNV毒株均引起了SIE;然而,在[此处原文缺失相关内容]中,EILV引起的SIE具有毒株特异性,这可能是由于各个WNV毒株消耗共享资源的速率不同所致。