4.8 Article

Bacterial effector targeting of a plant iron sensor facilitates iron acquisition and pathogen colonization

Journal

PLANT CELL
Volume 33, Issue 6, Pages 2015-2031

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/plcell/koab075

Keywords

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Funding

  1. Chinese Academy of Sciences [XDB11020300]
  2. Natural Science Foundation of China [31570252]
  3. startup fund of One Hundred Talents program of the Chinese Academy of Sciences
  4. State Key Laboratory of Plant Genomics [O8KF021011]
  5. National Institutes of Health [R35GM136402]
  6. USDA-NIFA [2015-67013-23082]
  7. Max-Planck Society, Germany's Excellence Strategy CEPLAS [EXC-2048/1, 390686111]
  8. Deutsche Forschungsgemeinschaft (DFG
  9. German Research Foundation) [CRC-680, CRC-1403414786233]

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The pathogen targets the plant iron sensor protein BRUTUS through the effector protein AvrRps4 to facilitate iron uptake and pathogen proliferation in Arabidopsis thaliana. AvrRps4 inhibits the degradation of iron regulatory proteins and enhances the accumulation of immune proteins, contributing to immune responses mediated by RPS4/EDS1.
Acquisition of nutrients from different species is necessary for pathogen colonization. Iron is an essential mineral nutrient for nearly all organisms, but little is known about how pathogens manipulate plant hosts to acquire iron. Here, we report that AvrRps4, an effector protein delivered by Pseudomonas syringae bacteria to plants, interacts with and targets the plant iron sensor protein BRUTUS (BTS) to facilitate iron uptake and pathogen proliferation in Arabidopsis thaliana. Infection of rps4 and eds1 by P. syringae pv. tomato (Pst) DC3000 expressing AvrRps4 resulted in iron accumulation, especially in the plant apoplast. AvrRps4 alleviates BTS-mediated degradation of bHLH115 and ILR3(IAA-Leucine resistant 3), two iron regulatory proteins. In addition, BTS is important for accumulating immune proteins Enhanced Disease Susceptibility1 (EDS1) at both the transcriptional and protein levels upon Pst (avrRps4) infections. Our findings suggest that AvrRps4 targets BTS to facilitate iron accumulation and BTS contributes to RPS4/EDS1-mediated immune responses.

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