Exploiting breakdown in nonhost effector-target interactions to boost host disease resistance

Hazel McLellan, Sarah E. Harvey, Jens Steinbrenner, Miles R. Armstrong, Qin He, Rachel Clewes, Leighton Pritchard, Wei Wang, Shumei Wang, Thomas Nussbaumer, Bushra Dohai, Qingquan Luo, Priyanka Kumari, Hui Duan, Ana Roberts, Petra C. Boevink, Christina Neumann, Nicolas Champouret, Ingo Hein, Pascal Falter-BraunJim Beynon, Katherine Denby (Lead / Corresponding author), Paul R. J. Birch (Lead / Corresponding author)

Research output: Contribution to journalArticlepeer-review

15 Citations (Scopus)
53 Downloads (Pure)


Plants are resistant to most microbial species due to nonhost resistance (NHR), providing broad-spectrum and durable immunity. However, the molecular components contributing to NHR are poorly characterised. We address the question of whether failure of pathogen effectors to manipulate nonhost plants plays a critical role in NHR. RxLR (Arg-any amino acid-Leu-Arg) effectors from two oomycete pathogens, Phytophthora infestans and Hyaloperonospora arabidopsidis, enhanced pathogen infection when expressed in host plants (Nicotiana benthamiana and Arabidopsis, respectively) but the same effectors performed poorly in distantly related nonhost pathosystems. Putative target proteins in the host plant potato were identified for 64 P. infestans RxLR effectors using yeast 2-hybrid (Y2H) screens. Candidate orthologues of these target proteins in the distantly related non-host plant Arabidopsis were identified and screened using matrix Y2H for interaction with RxLR effectors from both P. infestans and H. arabidopsidis. Few P. infestans effector-target protein interactions were conserved from potato to candidate Arabidopsis target orthologues (cAtOrths). However, there was an enrichment of H. arabidopsidis RxLR effectors interacting with cAtOrths. We expressed the cAtOrth AtPUB33, which unlike its potato orthologue did not interact with P. infestans effector PiSFI3, in potato and Nicotiana benthamiana. Expression of AtPUB33 significantly reduced P. infestans colonization in both host plants. Our results provide evidence that failure of pathogen effectors to interact with and/or correctly manipulate target proteins in distantly related non-host plants contributes to NHR. Moreover, exploiting this breakdown in effector-nonhost target interaction, transferring effector target orthologues from non-host to host plants is a strategy to reduce disease.

Original languageEnglish
Article numbere2114064119
Number of pages12
JournalProceedings of the National Academy of Sciences
Issue number35
Early online date22 Aug 2022
Publication statusPublished - 30 Aug 2022


  • host range
  • plant immunity
  • effector-triggered susceptibility
  • oomycete
  • plant-microbe interactions
  • late blight
  • plant–microbe interactions

ASJC Scopus subject areas

  • General


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