Comparative genomics identifies the M agnaporthe oryzae avirulence effector A vr P i9 that triggers P i9 ‐mediated blast resistance in rice

We identified the M agnaporthe oryzae avirulence effector A vr P i9 cognate to rice blast resistance gene P i9 by comparative genomics of requisite strains derived from a sequential planting method. AvrPi9 encodes a small secreted protein that appears to localize in the biotrophic interfacial comple...

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Veröffentlicht in:The New phytologist 2015-06, Vol.206 (4), p.1463-1475
Hauptverfasser: Wu, Jun, Kou, Yanjun, Bao, Jiandong, Li, Ya, Tang, Mingzhi, Zhu, Xiaoli, Ponaya, Ariane, Xiao, Gui, Li, Jinbin, Li, Chenyun, Song, Min‐Young, Cumagun, Christian Joseph R., Deng, Qiyun, Lu, Guodong, Jeon, Jong‐Seong, Naqvi, Naweed I., Zhou, Bo
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Sprache:eng
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Zusammenfassung:We identified the M agnaporthe oryzae avirulence effector A vr P i9 cognate to rice blast resistance gene P i9 by comparative genomics of requisite strains derived from a sequential planting method. AvrPi9 encodes a small secreted protein that appears to localize in the biotrophic interfacial complex and is translocated to the host cell during rice infection. AvrPi9 forms a tandem gene array with its paralogue proximal to centromeric region of chromosome 7. AvrPi9 is expressed highly at early stages during initiation of blast disease. Virulent isolate strains contain M g‐ SINE within the A vr P i9 coding sequence. Loss of A vr P i9 did not lead to any discernible defects during growth or pathogenesis in M . oryzae . This study reiterates the role of diverse transposable elements as off‐switch agents in acquisition of gain‐of‐virulence in the rice blast fungus. The prevalence of A vr P i9 correlates well with the avirulence pathotype in diverse blast isolates from the P hilippines and C hina, thus supporting the broad‐spectrum resistance conferred by P i9 in different rice growing areas. Our results revealed that P i9 and P iz‐t at the P i2/9 locus activate race specific resistance by recognizing sequence‐unrelated A vr P i9 and A vr P iz‐t genes, respectively.
ISSN:0028-646X
1469-8137
DOI:10.1111/nph.13310