Role of the SUT1 and SUT2 sugar transporters during stolbur phytoplasma infection in tomato

Abstract

SummaryPhytoplasmas inhabit phloem sieve elements and cause abnormal growth and altered sugar partitioning. But how they interact with phloem functions is not clearly known. The phloem responses were investigated in tomato infected by ‘Candidatus Phytoplasma solani’, at the beginning of the symptomatic stage of infection, both in symptomatic and asymptomatic leaves, the first symptoms appearing in the sink top leaf at the stem apex. Antisense lines impaired in the phloem sucrose transporters SUT1 and SUT2 were included. The infection in source leaves was not associated with symptoms. In the symptomatic, sink leaf, yellowing and leaf curling was associated with higher starch accumulation and expression of defense genes. The transcriptional analysis of symptomatic leaf midribs indicated that transcript levels for genes acting in the glycolysis and peroxisome metabolism in infected plants differed from these in non-infected plants. Phytoplasma multiplied actively in at least three additional lower leaves although they were symptomless, with no sign of activation of defense markers, although the rate of exudation of sucrose from these symptomless, source leaves was lower for infected plants. A few metabolites in phloem-enriched exudate were affected by the infection, such as glycolate and aspartate, and some of them were also affected in the control SUT1- and SUT2- antisense lines, in which sucrose retrieval or release in the sieve elements are impaired. A metabolic switch could explain the delivery of more glycolate into the sieve elements of infected plants. The findings suggest a link between sugar transport and redox homeostasis.One sentence summaryAn impairment of sucrose retrieval and release in the sieve elements occurs during phytoplasma infection, associated with changes in sugar and peroxisome metabolism

Increased susceptibility to Chrysanthemum Yellows phytoplasma infection in Atcals7 ko plants is accompanied by enhanced expression of carbohydrate transporters

“…7; Barratt et al, 2011), to provide precursors (i.e. UDP-glucose) for callose synthesis (Tan et al, 2015; De Marco et al, 2020), and for the production of carbon skeletons for synthesis of defense-related compounds (Bolouri-Moghaddam et al, 2010; Musetti et al, 2013). In Atcals7ko infected plants, increased photoassimilate investment into axial and additional sinks (such as phytoplasmas) would explain enhanced carbohydrate content and the up-regulation of AtSUS5 and AtSUS6 genes, which provide energy at the infection site (Yao et al, 2019; 2020).…”