4.5 Article

Host-Induced Gene Silencing in Barley Powdery Mildew Reveals a Class of Ribonuclease-Like Effectors

期刊

MOLECULAR PLANT-MICROBE INTERACTIONS
卷 26, 期 6, 页码 633-642

出版社

AMER PHYTOPATHOLOGICAL SOC
DOI: 10.1094/MPMI-01-13-0005-R

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资金

  1. Biotechnology and Biological Sciences Research Council [BB/H001646/1]
  2. European Union
  3. United States National Science Foundation (Plant Genome) [09-22746]
  4. Division Of Integrative Organismal Systems
  5. Direct For Biological Sciences [0922746] Funding Source: National Science Foundation
  6. Biotechnology and Biological Sciences Research Council [BB/H001646/1] Funding Source: researchfish
  7. BBSRC [BB/H001646/1] Funding Source: UKRI

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Obligate biotrophic pathogens of plants must circumvent or counteract defenses to guarantee accommodation inside the host. To do so, they secrete a variety of effectors that regulate host immunity and facilitate the establishment of pathogen feeding structures called haustoria. The barley powdery mildew fungus Blumeria graminis f. sp. hordei produces a large number of proteins predicted to be secreted from haustoria. Fifty of these Blumeria effector candidates (BEC) were screened by host-induced gene silencing (HIGS), and eight were identified that contribute to infection. One shows similarity to beta-1,3 glucosyltransferases, one to metallo-proteases, and two to microbial secreted ribonucleases; the remainder have no similarity to proteins of known function. Transcript abundance of all eight BEC increases dramatically in the early stages of infection and establishment of haustoria, consistent with a role in that process. Complementation analysis using silencing-insensitive synthetic cDNAs demonstrated that the ribonuclease-like BEC 1011 and 1054 are bona fide effectors that function within the plant cell. BEC1011 specifically interferes with pathogen-induced host cell death. Both are part of a gene superfamily unique to the powdery mildew fungi. Structural modeling was consistent, with BEC1054 adopting a ribonuclease-like fold, a scaffold not previously associated with effector function.

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