Host-interactor screens of Phytophthora infestans RXLR proteins reveal vesicle trafficking as a major effector-targeted process

Author:

Petre Benjamin12ORCID,Contreras Mauricio P1ORCID,Bozkurt Tolga O13ORCID,Schattat Martin H14ORCID,Sklenar Jan1ORCID,Schornack Sebastian15ORCID,Abd-El-Haliem Ahmed6ORCID,Castells-Graells Roger17ORCID,Lozano-Durán Rosa18ORCID,Dagdas Yasin F19ORCID,Menke Frank L H1ORCID,Jones Alexandra M E110ORCID,Vossen Jack H11ORCID,Robatzek Silke112ORCID,Kamoun Sophien1ORCID,Win Joe1ORCID

Affiliation:

1. The Sainsbury Laboratory, University of East Anglia, Norwich Research Park, Norwich, UK

2. Université de Lorraine, INRAE, IAM, Nancy, France

3. Department of Life Sciences, Imperial College London, London, UK

4. Department of Plant Physiology, Institute for Biology, Martin-Luther University Halle-Wittenberg, Halle, Germany

5. Sainsbury Laboratory, University of Cambridge, Cambridge, UK

6. Phytopathology Research, Rijk Zwaan Breeding BV, Fijnaart, The Netherlands

7. Molecular Biology Institute, University of California Los Angeles, Los Angeles, California, USA

8. Shanghai Center for Plant Stress Biology, CAS Center for Excellence in Molecular Plant Sciences, Chinese Academy of Sciences, Shanghai, China

9. Gregor Mendel Institute, Austrian Academy of Sciences, Vienna BioCenter, Vienna, Austria

10. School of Life Sciences, University of Warwick, Coventry, UK

11. Plant Breeding, Wageningen University and Research, Wageningen, The Netherlands

12. Ludwig-Maximilian-University of Munich, Munich, Germany

Abstract

Abstract Pathogens modulate plant cell structure and function by secreting effectors into host tissues. Effectors typically function by associating with host molecules and modulating their activities. This study aimed to identify the host processes targeted by the RXLR class of host-translocated effectors of the potato blight pathogen Phytophthora infestans. To this end, we performed an in planta protein–protein interaction screen by transiently expressing P. infestans RXLR effectors in Nicotiana benthamiana leaves followed by coimmunoprecipitation and liquid chromatography-tandem mass spectrometry. This screen generated an effector–host protein interactome matrix of 59 P. infestans RXLR effectors x 586 N. benthamiana proteins. Classification of the host interactors into putative functional categories revealed over 35 biological processes possibly targeted by P. infestans. We further characterized the PexRD12/31 family of RXLR-WY effectors, which associate and colocalize with components of the vesicle trafficking machinery. One member of this family, PexRD31, increased the number of FYVE positive vesicles in N. benthamiana cells. FYVE positive vesicles also accumulated in leaf cells near P. infestans hyphae, indicating that the pathogen may enhance endosomal trafficking during infection. This interactome dataset will serve as a useful resource for functional studies of P. infestans effectors and of effector-targeted host processes.

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Plant Science

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