禽类和蚊子宿主的 WNV 和 SLEV 共感染:对病毒血症、抗体反应和病媒能力的影响。

IF 4 2区 医学 Q2 VIROLOGY
Journal of Virology Pub Date : 2024-10-22 Epub Date: 2024-09-26 DOI:10.1128/jvi.01041-24
Emily N Gallichotte, Emily A Fitzmeyer, Landon Williams, Mark Cole Spangler, Angela M Bosco-Lauth, Gregory D Ebel
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引用次数: 0

摘要

西尼罗河病毒(WNV)和圣路易斯脑炎病毒(SLEV)是密切相关的黄病毒,可导致人类脑炎和动物的相关疾病。在自然界中,这两种病毒都是通过库蚊传播的,野生鸟类,包括松鸦、麻雀和知更鸟,都是脊椎动物的宿主。WNV 和 SLEV 在相同的环境中传播,最近在人类中同时引起了疾病爆发。然而,蚊子或鸟类的双重感染会在多大程度上改变传播动态,目前还没有很好的定论。因此,我们试图确定同时感染是否会改变鸟类的感染动力学和病毒水平以及蚊子的感染率。因此,我们用美国知更鸟(Turdus migratorius)、两种蚊子以及脊椎动物和无脊椎动物细胞感染了 WNV 和/或 SLEV,以评估同时暴露会如何改变感染结果。在脊椎动物细胞中,联合感染的影响各不相同,有证据表明 SLEV 可以抑制 WNV 的复制。然而,无论是否同时感染,知更鸟的病毒血症和抗体反应相当。相反,在库蚊细胞和蚊子中,我们发现同时暴露于两种病毒对复制的影响微乎其微,单一感染和混合感染蚊子的感染率、传播率和传染率相当。重要的是,虽然共感染蚊子中肠中的 WNV 和 SLEV 水平呈正相关,但我们在唾液腺和唾液中却没有发现它们之间的相关性。这些结果表明,虽然禽类宿主和蚊子宿主都可能发生共感染,但这两种病毒对彼此的影响微乎其微。重要意义西尼罗河病毒(WNV)和圣路易斯脑炎病毒(SLEV)是密切相关的病毒,它们由相同的蚊子传播,在自然界中感染相同的鸟类。这两种病毒在同一地区流行,并同时在人类中爆发。蚊子、鸟类和/或人类有可能同时感染 WNV 和 SLEV,正如在寨卡、基孔肯雅和登革热病毒中观察到的情况一样。为了研究共感染的影响,我们通过实验用 WNV 和/或 SLEV 感染了脊椎动物和无脊椎动物细胞、美国知更鸟以及两种库蚊。知更鸟能有效地合并感染,合并感染对病毒水平或免疫反应没有影响。同样,在蚊子中,混合感染也不会影响感染率,蚊子可以同时传播 WNV 和 SLEV。这些结果表明,鸟类和蚊子的 WNV 和 SLEV 共感染可能发生在自然界中,这可能会影响公共卫生和人类疾病风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
WNV and SLEV coinfection in avian and mosquito hosts: impact on viremia, antibody responses, and vector competence.

West Nile virus (WNV) and St. Louis encephalitis virus (SLEV) are closely related flaviviruses that can cause encephalitis in humans and related diseases in animals. In nature, both are transmitted by Culex, with wild birds, including jays, sparrows, and robins, serving as vertebrate hosts. WNV and SLEV circulate in the same environments and have recently caused concurrent disease outbreaks in humans. The extent that coinfection of mosquitoes or birds may alter transmission dynamics, however, is not well characterized. We therefore sought to determine if coinfection alters infection kinetics and virus levels in birds and infection rates in mosquitoes. Accordingly, American robins (Turdus migratorius), two species of mosquitoes, and vertebrate and invertebrate cells were infected with WNV and/or SLEV to assess how simultaneous exposure may alter infection outcomes. There was variable impact of coinfection in vertebrate cells, with some evidence that SLEV can suppress WNV replication. However, robins had comparable viremia and antibody responses regardless of coinfection. Conversely, in Culex cells and mosquitoes, we saw a minimal impact of simultaneous exposure to both viruses on replication, with comparable infection, dissemination, and transmission rates in singly infected and coinfected mosquitoes. Importantly, while WNV and SLEV levels in coinfected mosquito midguts were positively correlated, we saw no correlation between them in salivary glands and saliva. These results reveal that while coinfection can occur in both avian and mosquito hosts, the viruses minimally impact one another. The potential for coinfection to alter virus population structure or the likelihood of rare genotypes emerging remains unknown.IMPORTANCEWest Nile virus (WNV) and St. Louis encephalitis virus (SLEV) are closely related viruses that are transmitted by the same mosquitoes and infect the same birds in nature. Both viruses circulate in the same regions and have caused concurrent outbreaks in humans. It is possible that mosquitoes, birds, and/or humans could be infected with both WNV and SLEV simultaneously, as has been observed with Zika, chikungunya, and dengue viruses. To study the impact of coinfection, we experimentally infected vertebrate and invertebrate cells, American robins, and two Culex species with WNV and/or SLEV. Robins were efficiently coinfected, with no impact of coinfection on virus levels or immune response. Similarly, in mosquitoes, coinfection did not impact infection rates, and mosquitoes could transmit both WNV and SLEV together. These results reveal that WNV and SLEV coinfection in birds and mosquitoes can occur in nature, which may impact public health and human disease risk.

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来源期刊
Journal of Virology
Journal of Virology 医学-病毒学
CiteScore
10.10
自引率
7.40%
发文量
906
审稿时长
1 months
期刊介绍: Journal of Virology (JVI) explores the nature of the viruses of animals, archaea, bacteria, fungi, plants, and protozoa. We welcome papers on virion structure and assembly, viral genome replication and regulation of gene expression, genetic diversity and evolution, virus-cell interactions, cellular responses to infection, transformation and oncogenesis, gene delivery, viral pathogenesis and immunity, and vaccines and antiviral agents.
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