Literature DB >> 35864318

Host nuclear repositioning and actin polarization towards the site of penetration precedes fungal ingress during compatible pea-powdery mildew interactions.

Akriti Sharma1, Divya Chandran2.   

Abstract

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CONCLUSION: Actin polarization and actin-driven host nuclear movement towards the fungal penetration site facilitates successful host colonization during compatible pea-Erysiphe pisi interactions. Proper nuclear positioning in plant cells is crucial for developmental processes and response to (a)biotic stimuli. During plant-fungal interactions, the host nucleus moves toward the infection site, a process regulated by the plant cytoskeleton. Notably, rearrangement of the plant cytoskeleton is one of the earliest cellular responses to pathogen invasion and is known to impact penetration efficiency. Yet, the connection between host nuclear movement and fungal ingress is still elusive, particularly in legumes. Here, we investigated the host nuclear dynamics during compatible interactions between Pisum sativum (pea) and the adapted powdery mildew (PM) fungus Erysiphe pisi to gain insights into the functional relevance of PM-induced nuclear movement in legumes. We show that the host nucleus moves towards the fungal appressorium before penetration and becomes associated with the primary haustorium. However, the nucleus migrates away from the primary infection site as the infection progresses toward colony expansion and sporulation. Treatment of pea leaves with the actin-polymerization inhibitor, cytochalasin D, abolished host nuclear movement towards the fungal penetration site and restricted PM growth. In contrast, treatment with oryzalin, a microtubule-polymerization inhibitor, had no effect. In addition to nuclear movement, strong polarization of host actin filaments towards the site of appressorial contact was evident at early infection stages. Our results suggest that actin focusing mediates host nuclear movement to the fungal penetration site and facilitates successful colonization during compatible pea-PM interactions.
© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Entities:  

Keywords:  Biotrophic interactions; Cytoskeleton; Erysiphe pisi; Legume; Nuclear movement; Pisum sativum

Mesh:

Substances:

Year:  2022        PMID: 35864318     DOI: 10.1007/s00425-022-03959-3

Source DB:  PubMed          Journal:  Planta        ISSN: 0032-0935            Impact factor:   4.540


  28 in total

Review 1.  Check-in procedures for plant cell entry by biotrophic microbes.

Authors:  Andrea Genre; Paola Bonfante
Journal:  Mol Plant Microbe Interact       Date:  2007-09       Impact factor: 4.171

Review 2.  Cell-autonomous defense, re-organization and trafficking of membranes in plant-microbe interactions.

Authors:  Peter Dörmann; Hyeran Kim; Thomas Ott; Paul Schulze-Lefert; Marco Trujillo; Vera Wewer; Ralph Hückelhoven
Journal:  New Phytol       Date:  2014-08-28       Impact factor: 10.151

3.  A barley ROP GTPase ACTIVATING PROTEIN associates with microtubules and regulates entry of the barley powdery mildew fungus into leaf epidermal cells.

Authors:  Caroline Hoefle; Christina Huesmann; Holger Schultheiss; Frederik Börnke; Götz Hensel; Jochen Kumlehn; Ralph Hückelhoven
Journal:  Plant Cell       Date:  2011-06-17       Impact factor: 11.277

4.  Solute transport into healthy and powdery mildew-infected leaves of pea and uptake by powdery mildew mycelium.

Authors:  Joanna I M Clark; J L Hall
Journal:  New Phytol       Date:  1998-10       Impact factor: 10.151

5.  Quantitative analyses on dynamic changes in the organization of host Arabidopsis thaliana actin microfilaments surrounding the infection organ of the powdery mildew fungus Golovinomyces orontii.

Authors:  Noriko Inada; Takumi Higaki; Seiichiro Hasezawa
Journal:  J Plant Res       Date:  2015-12-08       Impact factor: 2.629

6.  Dual RNA-Seq analysis of Medicago truncatula and the pea powdery mildew Erysiphe pisi uncovers distinct host transcriptional signatures during incompatible and compatible interactions and pathogen effector candidates.

Authors:  Megha Gupta; Gunjan Sharma; Divya Saxena; Roli Budhwar; Madavan Vasudevan; Varsha Gupta; Arunima Gupta; Rashi Gupta; Divya Chandran
Journal:  Genomics       Date:  2019-12-16       Impact factor: 5.736

7.  Biotic and abiotic stimulation of root epidermal cells reveals common and specific responses to arbuscular mycorrhizal fungi.

Authors:  Andrea Genre; Giuseppe Ortu; Chiara Bertoldo; Elena Martino; Paola Bonfante
Journal:  Plant Physiol       Date:  2009-01-16       Impact factor: 8.340

8.  Arbuscular mycorrhizal fungi elicit a novel intracellular apparatus in Medicago truncatula root epidermal cells before infection.

Authors:  Andrea Genre; Mireille Chabaud; Ton Timmers; Paola Bonfante; David G Barker
Journal:  Plant Cell       Date:  2005-11-11       Impact factor: 11.277

9.  Translocation of cytoplasm and nucleus to fungal penetration sites is associated with depolymerization of microtubules and defence gene activation in infected, cultured parsley cells.

Authors:  P Gross; C Julius; E Schmelzer; K Hahlbrock
Journal:  EMBO J       Date:  1993-05       Impact factor: 11.598

Review 10.  Nuclei in motion: movement and positioning of plant nuclei in development, signaling, symbiosis, and disease.

Authors:  Anna H N Griffis; Norman R Groves; Xiao Zhou; Iris Meier
Journal:  Front Plant Sci       Date:  2014-04-03       Impact factor: 5.753

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