Centro Internacional de Entrenamiento e Investigaciones Médicas (CIDEIM), Cali, Colombia.
W. Harry Feinstone Department of Molecular Microbiology and Immunology, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland, USA.
Insect Sci. 2019 Aug;26(4):635-648. doi: 10.1111/1744-7917.12573. Epub 2018 Apr 6.
Aedes (Stegomyia) aegypti, the principal global vector of dengue viruses, has differences in its susceptibility to dengue virus infection. We compared the global expression of genes in the midguts of Colombian Ae. aegypti dengue-susceptible (Cali-S) and dengue-refractory (Cali-MIB) field derived strains after ingesting either a sugarmeal, a bloodmeal, or a bloodmeal containing dengue virus serotype 2 (DENV-2). Microarray-based transcriptome analysis among treatments indicated a total of 4725 transcripts with differential expression between the two strains. Eleven genes were selected from different functional groups based on their significant up or down expression levels as well as reports in the literature suggesting they are associated with dengue virus elimination. We measured mRNA abundance of these 11 genes at 0, 8, 24, and 36 h postinfection using quantitative real time PCR (qPCR) to confirm the microarray results and assess any temporal patterns. Four genes were selected (Gram-negative binding protein-GNBP [AAEL009176], Niemann Pick Type-C2-NPC2 [AAEL015136], Keratinocyte lectin [AAEL009842], and Cathepsin-b [AAEL007585]) for knockdown experiments using RNA interference (RNAi) methodology to determine the phenotype (DENV-2 susceptible or refractory). Silencing GNBP, Cathepsin-b and Keratinocyte lectin reduced the percentage of mosquitoes with disseminated virus in the Cali-S strain to 8%, 20%, and 12% respectively compared with 96% in the controls. Silencing of NPC2 increased the percentage of mosquitos with disseminated virus infections in Cali-MIB to 66% compared with 35% in the controls. This study provides insight into genes that may contribute to the Cali-S susceptible and Cali-MIB refractory phenotypes in Ae. aegypti.
埃及伊蚊(Stegomyia)是登革热病毒的主要全球传播媒介,其对登革热病毒感染的易感性存在差异。我们比较了摄入糖餐、血餐或含登革热病毒血清型 2(DENV-2)的血餐后,来自哥伦比亚的登革热易感(Cali-S)和登革热抗性(Cali-MIB)田间衍生株的中肠的全球基因表达。处理之间的基于微阵列的转录组分析表明,两种菌株之间有 4725 个转录本存在差异表达。根据它们显著的上调或下调表达水平以及文献报道,我们从不同的功能组中选择了 11 个基因,这些基因与登革热病毒的消除有关。我们使用定量实时 PCR(qPCR)在感染后 0、8、24 和 36 小时测量这些 11 个基因的 mRNA 丰度,以确认微阵列结果并评估任何时间模式。选择了 4 个基因(革兰氏阴性结合蛋白-GNBP [AAEL009176]、神经鞘脂类胆固醇转移酶 2-NPC2 [AAEL015136]、角蛋白细胞凝集素 [AAEL009842] 和组织蛋白酶 b [AAEL007585])进行 RNA 干扰(RNAi)方法的基因敲低实验,以确定表型(对 DENV-2 敏感或抗性)。与对照组的 96%相比,沉默 GNBP、组织蛋白酶 b 和角蛋白细胞凝集素使 Cali-S 株中具有传播性病毒的蚊子百分比分别降低到 8%、20%和 12%。沉默 NPC2 使 Cali-MIB 中具有传播性病毒感染的蚊子百分比增加到 66%,而对照组为 35%。这项研究提供了有关可能导致埃及伊蚊 Cali-S 易感和 Cali-MIB 抗性表型的基因的见解。