Harris Emma K, Balaraman Velmurugan, Keating Cassidy C, McDowell Chester, Kimble J Brian, De La Mota-Peynado Alina, Borland Erin M, Graham Barbara, Wilson William C, Richt Juergen A, Kading Rebekah C, Gaudreault Natasha N
Center for Vector-Borne Infectious Diseases, Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, CO 80523, USA.
Center of Excellence for Emerging and Zoonotic Animal Diseases, Diagnostic Medicine/Pathobiology, Kansas State University, Manhattan, KS 66506, USA.
Viruses. 2025 Jan 11;17(1):88. doi: 10.3390/v17010088.
Rift Valley fever phlebovirus (RVFV) is a zoonotic mosquito-borne pathogen endemic to sub-Saharan Africa and the Arabian Peninsula which causes Rift Valley fever in ruminant livestock and humans. Co-infection with divergent viral strains can produce reassortment among the L, S, and M segments of the RVFV genome. Reassortment events can produce novel genotypes with altered virulence, transmission dynamics, and/or mosquito host range. This can have severe implications in areas where RVFV is endemic and convolutes our ability to anticipate transmission and circulation in novel geographic regions. Previously, we evaluated the frequency of RVFV reassortment in a susceptible ruminant host and observed low rates of reassortment (0-1.7%). Here, we tested the hypothesis that reassortment occurs predominantly in the mosquito using a highly permissive vector, . Cells derived from or adult mosquitoes were co-infected with either two virulent (Kenya-128B-15 and SA01-1322) or a virulent and attenuated (Kenya-128B-15 and MP-12) strain of RVFV. Our results showed approximately 2% of virus genotypes isolated from co-infected -derived cells were reassortant. Co-infected mosquitoes infected via infectious bloodmeal resulted in a higher percentage of reassortant virus (2-60%) isolated from midgut and salivary tissues at 14 days post-infection. The percentage of reassortant genotypes isolated from the midguts of mosquitoes co-infected with Kenya-128B-15 and SA01-1322 was similar to that of mosquitoes co-infected with Kenya-128B-15 and MP-12- strains (60 vs. 47%). However, only 2% of virus isolated from the salivary glands of Kenya-128B-15 and SA01-1322 co-infected mosquitoes represented reassortant genotypes. This was contrasted by 54% reassortment in the salivary glands of mosquitoes co-infected with Kenya-128B-15 and MP-12 strains. Furthermore, we observed preferential inclusion of genomic segments from the three parental strains among the reassorted viruses. Replication curves of select reassorted genotypes were significantly higher in Vero cells but not in -derived cells. These data imply that mosquitoes play a crucial role in the reassortment of RVFV and potentially contribute to driving evolution of the virus.
裂谷热静脉病毒(RVFV)是一种人畜共患的蚊媒病原体,在撒哈拉以南非洲和阿拉伯半岛流行,可导致反刍家畜和人类患裂谷热。与不同病毒株的共同感染可导致RVFV基因组的L、S和M片段之间发生重配。重配事件可产生具有改变的毒力、传播动态和/或蚊宿主范围的新基因型。这在RVFV流行的地区可能会产生严重影响,并使我们预测病毒在新地理区域的传播和循环的能力变得复杂。此前,我们评估了RVFV在易感反刍动物宿主中的重配频率,观察到重配率较低(0-1.7%)。在此,我们使用一种高度易感的载体—— 来检验重配主要发生在蚊子体内的假设。从 或成年蚊子中提取的细胞与两种强毒株(肯尼亚-128B-15和SA01-1322)或一种强毒株和一种弱毒株(肯尼亚-128B-15和MP-12)的RVFV共同感染。我们的结果显示,从共同感染的 -来源细胞中分离出的病毒基因型中约2%是重配型。通过感染性血餐感染的共同感染蚊子,在感染后14天,从中肠和唾液组织中分离出的重配病毒比例更高(2-60%)。从与肯尼亚-128B-15和SA01-1322共同感染的蚊子中肠分离出的重配基因型比例与与肯尼亚-128B-15和MP-12毒株共同感染的蚊子相似(60%对47%)。然而,从与肯尼亚-128B-15和SA01-1322共同感染的蚊子唾液腺中分离出的病毒中,只有2%代表重配基因型。与之形成对比的是,与肯尼亚-128B-15和MP-12毒株共同感染的蚊子唾液腺中的重配率为54%。此外,我们观察到在重配病毒中优先包含来自三种亲代毒株的基因组片段。选择的重配基因型在Vero细胞中的复制曲线显著更高,但在 -来源细胞中则不然。这些数据表明,蚊子在RVFV重配中起关键作用,并可能有助于推动病毒的进化。