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Virulence strategies of an insect herbivore and oomycete plant pathogen converge on host E3 SUMO ligase SIZ1

Pathogens and pests secrete proteins (effectors) to interfere with plant immunity through modification of host target functions and disruption of immune signalling networks. The extent of convergence between pathogen and herbivorous insect virulence strategies is largely unexplored. We found that ef...

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Autores principales: Liu, Shan, Lenoir, Camille J. G., Amaro, Tiago M. M. M., Rodriguez, Patricia A., Huitema, Edgar, Bos, Jorunn I. B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9545238/
https://www.ncbi.nlm.nih.gov/pubmed/35491752
http://dx.doi.org/10.1111/nph.18184
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author Liu, Shan
Lenoir, Camille J. G.
Amaro, Tiago M. M. M.
Rodriguez, Patricia A.
Huitema, Edgar
Bos, Jorunn I. B.
author_facet Liu, Shan
Lenoir, Camille J. G.
Amaro, Tiago M. M. M.
Rodriguez, Patricia A.
Huitema, Edgar
Bos, Jorunn I. B.
author_sort Liu, Shan
collection PubMed
description Pathogens and pests secrete proteins (effectors) to interfere with plant immunity through modification of host target functions and disruption of immune signalling networks. The extent of convergence between pathogen and herbivorous insect virulence strategies is largely unexplored. We found that effectors from the oomycete pathogen, Phytophthora capsici, and the major aphid pest, Myzus persicae target the host immune regulator SIZ1, an E3 SUMO ligase. We used transient expression assays in Nicotiana benthamiana as well as Arabidopsis mutants to further characterize biological role of effector–SIZ1 interactions in planta. We show that the oomycete and aphid effector, which both contribute to virulence, feature different activities towards SIZ1. While M. persicae effector Mp64 increases SIZ1 protein levels in transient assays, P. capsici effector CRN83_152 enhances SIZ1‐E3 SUMO ligase activity in vivo. SIZ1 contributes to host susceptibility to aphids and an oomycete pathogen. Knockout of SIZ1 in Arabidopsis decreased susceptibility to aphids, independent of SNC1, PAD4 and EDS1. Similarly SIZ1 knockdown in N. benthamiana led to reduced P. capsici infection. Our results suggest convergence of distinct pathogen and pest virulence strategies on an E3 SUMO ligase to enhance host susceptibility.
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spelling pubmed-95452382022-10-14 Virulence strategies of an insect herbivore and oomycete plant pathogen converge on host E3 SUMO ligase SIZ1 Liu, Shan Lenoir, Camille J. G. Amaro, Tiago M. M. M. Rodriguez, Patricia A. Huitema, Edgar Bos, Jorunn I. B. New Phytol Research Pathogens and pests secrete proteins (effectors) to interfere with plant immunity through modification of host target functions and disruption of immune signalling networks. The extent of convergence between pathogen and herbivorous insect virulence strategies is largely unexplored. We found that effectors from the oomycete pathogen, Phytophthora capsici, and the major aphid pest, Myzus persicae target the host immune regulator SIZ1, an E3 SUMO ligase. We used transient expression assays in Nicotiana benthamiana as well as Arabidopsis mutants to further characterize biological role of effector–SIZ1 interactions in planta. We show that the oomycete and aphid effector, which both contribute to virulence, feature different activities towards SIZ1. While M. persicae effector Mp64 increases SIZ1 protein levels in transient assays, P. capsici effector CRN83_152 enhances SIZ1‐E3 SUMO ligase activity in vivo. SIZ1 contributes to host susceptibility to aphids and an oomycete pathogen. Knockout of SIZ1 in Arabidopsis decreased susceptibility to aphids, independent of SNC1, PAD4 and EDS1. Similarly SIZ1 knockdown in N. benthamiana led to reduced P. capsici infection. Our results suggest convergence of distinct pathogen and pest virulence strategies on an E3 SUMO ligase to enhance host susceptibility. John Wiley and Sons Inc. 2022-05-28 2022-08 /pmc/articles/PMC9545238/ /pubmed/35491752 http://dx.doi.org/10.1111/nph.18184 Text en © 2022 The Authors. New Phytologist © 2022 New Phytologist Foundation https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Liu, Shan
Lenoir, Camille J. G.
Amaro, Tiago M. M. M.
Rodriguez, Patricia A.
Huitema, Edgar
Bos, Jorunn I. B.
Virulence strategies of an insect herbivore and oomycete plant pathogen converge on host E3 SUMO ligase SIZ1
title Virulence strategies of an insect herbivore and oomycete plant pathogen converge on host E3 SUMO ligase SIZ1
title_full Virulence strategies of an insect herbivore and oomycete plant pathogen converge on host E3 SUMO ligase SIZ1
title_fullStr Virulence strategies of an insect herbivore and oomycete plant pathogen converge on host E3 SUMO ligase SIZ1
title_full_unstemmed Virulence strategies of an insect herbivore and oomycete plant pathogen converge on host E3 SUMO ligase SIZ1
title_short Virulence strategies of an insect herbivore and oomycete plant pathogen converge on host E3 SUMO ligase SIZ1
title_sort virulence strategies of an insect herbivore and oomycete plant pathogen converge on host e3 sumo ligase siz1
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9545238/
https://www.ncbi.nlm.nih.gov/pubmed/35491752
http://dx.doi.org/10.1111/nph.18184
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