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Effects of Manipulating Apoptosis on Sindbis Virus Infection of Aedes aegypti Mosquitoes

机译:操纵细胞凋亡对埃及伊蚊的信德比斯病毒感染的影响。

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摘要

Improved control of vector-borne diseases requires an understanding of the molecular factors that determine vector competence. Apoptosis has been shown to play a role in defense against viruses in insects and mammals. Although some observations suggest a correlation between apoptosis and resistance to arboviruses in mosquitoes, there is no direct evidence tying apoptosis to arbovirus vector competence. To determine whether apoptosis can influence arbovirus replication in mosquitoes, we manipulated apoptosis in Aedes aegypti mosquitoes by silencing the expression of genes that either positively or negatively regulate apoptosis. Silencing of the A. aegypti anti-apoptotic gene iap1 (Aeiap1) caused apoptosis in midgut epithelium, alterations in midgut morphology, and 60 to 70% mosquito mortality. Mortality induced by Aeiap1 silencing was rescued by cosilencing the initiator caspase gene Aedronc, indicating that the mortality was due to apoptosis. When mosquitoes which had been injected with Aeiap1 double-stranded RNA (dsRNA) were orally infected with Sindbis virus (SINV), increased midgut infection and virus dissemination to other organs were observed. This increase in virus infection may have been due to the effects of widespread apoptosis on infection barriers or innate immunity. In contrast, silencing the expression of Aedronc, which would be expected to inhibit apoptosis, reduced SINV midgut infection and virus dissemination. Thus, our data suggest that some level of caspase activity and/or apoptosis may be necessary for efficient virus replication and dissemination in mosquitoes. This is the first study to directly test the roles of apoptosis and caspases in determining mosquito vector competence for arboviruses.
机译:改善对媒介传播疾病的控制,需要了解决定媒介能力的分子因素。细胞凋亡已被证明对昆虫和哺乳动物的病毒具有防御作用。尽管一些观察结果表明细胞凋亡与蚊虫对虫媒病毒的抗性之间存在相关性,但尚无直接证据将细胞凋亡与虫媒病毒载体能力相关联。为了确定凋亡是否可以影响虫媒病毒在蚊子中的复制,我们通过沉默正向或负向调控细胞凋亡的基因的表达来操纵埃及伊蚊的凋亡。埃及伊蚊抗凋亡基因iap1(Aeiap1)的沉默导致中肠上皮细胞凋亡,中肠形态改变和60%至70%的蚊子死亡率。通过使启动子半胱天冬酶基因Aedronc相互沉默可以挽救Aeiap1沉默引起的死亡率,这表明死亡率是由于细胞凋亡引起的。当将注射有Aeiap1双链RNA(dsRNA)的蚊子口服辛德比斯病毒(SINV)感染时,观察到中肠感染增加,并且病毒传播到其他器官。病毒感染的增加可能是由于广泛的细胞凋亡对感染屏障或先天免疫的影响。相反,沉默Aedronc的表达可望抑制细胞凋亡,减少SINV中肠感染和病毒传播。因此,我们的数据表明某种水平的半胱天冬酶活性和/或凋亡可能是有效的病毒复制和在蚊子中传播所必需的。这是第一个直接测试凋亡和胱天蛋白酶在确定蚊媒对虫媒病毒能力中的作用的研究。

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