Phytophthora sojae apoplastic effector AEP1 mediates sugar uptake by mutarotation of extracellular aldose and is recognized as a MAMP.
Yuanpeng XuYunhuan ZhangJinyin ZhuYujing SunBaodian GuoFan LiuJie HuangHaonan WangSuomeng DongXiaobo ZhengYuan-Chao WangPublished in: Plant physiology (2022)
Diseases caused by Phytophthora pathogens devastate many crops worldwide. During infection, Phytophthora pathogens secrete effectors, which are central molecules for understanding the complex plant-Phytophthora interactions. In this study, we profiled the effector repertoire secreted by Phytophthora sojae into the soybean (Glycine max) apoplast during infection using liquid chromatography-mass spectrometry. A secreted aldose 1-epimerase (AEP1) was shown to induce cell death in Nicotiana benthamiana, as did the other two AEP1s from different Phytophthora species. AEP1 could also trigger immune responses in N. benthamiana, other Solanaceae plants, and Arabidopsis (Arabidopsis thaliana). A glucose dehydrogenase assay revealed AEP1 encodes an active AEP1. The enzyme activity of AEP1 is dispensable for AEP1-triggered cell death and immune responses, while AEP-triggered immune signaling in N. benthamiana requires the central immune regulator BRASSINOSTEROID INSENSITIVE 1-associated receptor kinase 1. In addition, AEP1 acts as a virulence factor that mediates P. sojae extracellular sugar uptake by mutarotation of extracellular aldose from the α-anomer to the β-anomer. Taken together, these results revealed the function of a microbial apoplastic effector, highlighting the importance of extracellular sugar uptake for Phytophthora infection. To counteract, the key effector for sugar conversion can be recognized by the plant membrane receptor complex to activate plant immunity.
Keyphrases
- cell death
- mass spectrometry
- immune response
- dendritic cells
- liquid chromatography
- regulatory t cells
- type iii
- antimicrobial resistance
- transcription factor
- escherichia coli
- microbial community
- toll like receptor
- staphylococcus aureus
- single cell
- cystic fibrosis
- metabolic syndrome
- ms ms
- cell proliferation
- signaling pathway
- insulin resistance
- protein kinase
- pi k akt