Chisenhall Daniel M, Christofferson Rebecca C, McCracken Michael K, Johnson Ann-Marie F, Londono-Renteria Berlin, Mores Christopher N
Department of Pathobiological Sciences, Vector-borne Disease Laboratories, Louisiana State University, School of Veterinary Medicine, Baton Rouge, LA, USA.
Parasit Vectors. 2014 May 30;7:252. doi: 10.1186/1756-3305-7-252.
Dengue virus (DENV) is responsible for up to approximately 300 million infections and an increasing number of deaths related to severe manifestations each year in affected countries throughout the tropics. It is critical to understand the drivers of this emergence, including the role of vector-virus interactions. When a DENV-infected Aedes aegypti mosquito bites a vertebrate, the virus is deposited along with a complex mixture of salivary proteins. However, the influence of a DENV infection upon the expectorated salivary proteome of its vector has yet to be determined.
Therefore, we conducted a proteomic analysis using 2-D gel electrophoresis coupled with mass spectrometry based protein identification comparing the naturally expectorated saliva of Aedes aegypti infected with DENV-2 relative to that of uninfected Aedes aegypti.
Several proteins were found to be differentially expressed in the saliva of DENV-2 infected mosquitoes, in particular proteins with anti-hemostatic and pain inhibitory functions were significantly reduced. Hypothetical consequences of these particular protein reductions include increased biting rates and transmission success, and lead to alteration of transmission potential as calculated in our vectorial capacity model.
We present our characterizations of these changes with regards to viral transmission and mosquito blood-feeding success. Further, we conclude that our proteomic analysis of Aedes aegypti saliva altered by DENV infection provides a unique opportunity to identify pro-viral impacts key to virus transmission.
登革病毒(DENV)每年在热带地区的受影响国家导致多达约3亿人感染,且与严重症状相关的死亡人数不断增加。了解这种情况出现的驱动因素至关重要,包括病媒与病毒相互作用的作用。当一只感染登革病毒的埃及伊蚊叮咬脊椎动物时,病毒会与唾液蛋白的复杂混合物一起被注入。然而,登革病毒感染对其病媒咳出的唾液蛋白质组的影响尚未确定。
因此,我们进行了一项蛋白质组学分析,使用二维凝胶电泳结合基于质谱的蛋白质鉴定,比较感染登革病毒2型的埃及伊蚊与未感染的埃及伊蚊自然咳出的唾液。
发现几种蛋白质在感染登革病毒2型的蚊子唾液中差异表达,特别是具有抗止血和止痛功能的蛋白质显著减少。这些特定蛋白质减少的假设后果包括叮咬率增加和传播成功率提高,并导致我们的病媒传播能力模型计算出的传播潜力改变。
我们展示了这些与病毒传播和蚊子吸血成功相关变化的特征。此外,我们得出结论,我们对受登革病毒感染而改变的埃及伊蚊唾液进行的蛋白质组学分析为识别病毒传播关键的促病毒影响提供了独特机会。