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Infection by chikungunya virus modulates the expression of several proteins in Aedes aegypti salivary glands

机译:基孔肯雅病毒感染可调节埃及伊蚊唾液腺中几种蛋白质的表达

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Background Arthropod-borne viral infections cause several emerging and resurging infectious diseases. Among the diseases caused by arboviruses, chikungunya is responsible for a high level of severe human disease worldwide. The salivary glands of mosquitoes are the last barrier before pathogen transmission. Methods We undertook a proteomic approach to characterize the key virus/vector interactions and host protein modifications that occur in the salivary glands that could be responsible for viral transmission by using quantitative two-dimensional electrophoresis. Results We defined the protein modulations in the salivary glands of Aedes aegypti that were triggered 3 and 5 days after an oral infection (3 and 5 DPI) with chikungunya virus (CHIKV). Gel profile comparisons showed that CHIKV at 3 DPI modulated the level of 13 proteins, and at 5 DPI 20 proteins. The amount of 10 putatively secreted proteins was regulated at both time points. These proteins were implicated in blood-feeding or in immunity, but many have no known function. CHIKV also modulated the quantity of proteins involved in several metabolic pathways and in cell signalling. Conclusion Our study constitutes the first analysis of the protein response of Aedes aegypti salivary glands infected with CHIKV. We found that the differentially regulated proteins in response to viral infection include structural proteins and enzymes for several metabolic pathways. Some may favour virus survival, replication and transmission, suggesting a subversion of the insect cell metabolism by arboviruses. For example, proteins involved in blood-feeding such as the short D7, an adenosine deaminase and inosine-uridine preferring nucleoside hydrolase, may favour virus transmission by exerting an increased anti-inflammatory effect. This would allow the vector to bite without the bite being detected. Other proteins, like the anti-freeze protein, may support vector protection.
机译:背景技术节肢动物传播的病毒感染会引起几种新出现和流行的传染病。在虫媒病毒引起的疾病中,基孔肯雅热是导致全球范围内严重人类疾病的高度原因。蚊子的唾液腺是病原体传播之前的最后障碍。方法我们采用蛋白质组学方法,通过定量二维电泳来表征唾液腺中可能与病毒传播有关的关键病毒/载体相互作用和宿主蛋白修饰。结果我们定义了埃及伊蚊唾液腺中的蛋白调节,这些蛋白是在基孔肯雅病毒(CHIKV)口腔感染(3和5 DPI)后3天和5天触发的。凝胶谱比较显示,CHIKV在3 DPI时可调节13种蛋白质的水平,在5 DPI 20时可调节蛋白质的水平。在两个时间点都调节了10种假定分泌的蛋白质的量。这些蛋白与血液喂养或免疫有关,但许多蛋白尚不知道。 CHIKV还调节了几种代谢途径和细胞信号传导中涉及的蛋白质数量。结论我们的研究构成了感染CHIKV的埃及伊蚊唾液腺蛋白反应的首次分析。我们发现响应病毒感染的差异调节蛋白包括结构蛋白和几种代谢途径的酶。有些可能会有利于病毒的生存,复制和传播,这表明虫媒病毒会破坏昆虫细胞的新陈代谢。例如,参与血液喂养的蛋白质,例如短D7,腺苷脱氨酶和肌苷-尿苷偏爱核苷水解酶,可能通过发挥增强的抗炎作用而促进病毒传播。这将允许矢量咬合而不会被检测到咬合。其他蛋白质,例如抗冻蛋白质,可能支持载体保护。

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