Loss of The Phloem-Expressed Sugar Transporter VST1 Reduces Aphid Performance In Watermelon
Abstract Aphids can damage plants through sugar withdrawal by hijacking sugar metabolism and transport genes to increase their sugar sucking ability. Blocking plant diseases and pest access to nutrients has emerged as an exciting strategy for improving disease and insect resistance in plants. Our previous work identified a shift in the localization of the vacuolar sugar transporter (VST1) that contributes to sucrose (Suc) and glucose (Glc) unloading in the phloem of sweet watermelons. In this study, the potential role of VST1 in the response to aphid infestation was investigated. Loss of VST1 function adversely impacted aphid settling and honeydew production. The vst1 mutant displayed less aphid-induced hydrogen peroxide accumulation and cell death than wild-type (WT) plants. Additionally, the expression of the VST1 gene was induced by aphids. The mutation of VST1 reduced Suc and Glc accumulation in the phloem, indicating that Suc and Glc are important carbohydrate substrates in phloem sap that are transported by VST1 to support aphid propagation and infestation. Taken together, our results demonstrated that the mutation of VST1 by genome editing can decrease aphid performance in watermelon by blocking the sugar supply obtained from phloem sap.