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

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 mi...

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Veröffentlicht in:Molecular plant-microbe interactions 2013-06, Vol.26 (6), p.633-642
Hauptverfasser: PLIEGO, Clara, NOWARA, Daniela, SCHWEIZER, Patrick, BINDSCHEDLER, Laurence V, SPANU, Pietro D, BONCIANI, Giulia, GHEORGHE, Dana M, RUO XU, SURANA, Priyanka, WHIGHAM, Ehren, NETTLETON, Dan, BOGDANOVE, Adam J, WISE, Roger P
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Sprache:eng
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Zusammenfassung: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 β-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.
ISSN:0894-0282
1943-7706
DOI:10.1094/mpmi-01-13-0005-r