Abstract
Powdery mildews are biotrophic pathogens causing fungal diseases in many economically important crops, including cereals, which are affected by Blumeria graminis. Powdery mildews only invade the epidermal cell layer of leaf tissues, in which they form haustorial structures. Haustoria are at the center of the biotrophic interaction by taking up nutrients from the host and by delivering effectors in the invaded cells to jeopardize plant immunity. Haustoria are composed of a fungal core delimited by a haustorial plasma membrane and cell wall. Surrounding these is the extrahaustorial complex, of which the extrahaustorial membrane is of plant origin. Although haustoria transcriptomes and proteomes have been investigated for Blumeria, the proteomes of barley epidermis upon infection and the barley components of the extrahaustorial complex remains unexplored. When comparing proteomes of infected and non-infected epidermis, several classical pathogenesis-related (PR) proteins were more abundant in infected epidermis. These included peroxidases, chitinases, cysteine-rich venom secreted proteins/PR1 and two thaumatin-like PR5 protein isoforms, of which TLP5 was previously shown to interact with the Blumeria effector BEC1054 (CSEP0064). Against expectations, transient TLP5 gene silencing suggested that TLP5 does not contribute to resistance but modulates susceptibility towards B. graminis. In a second proteomics comparison, haustorial structures were enriched from infected epidermal strips to identify plant proteins closely associated with the extrahaustorial complex. In these haustoria-enriched samples, relative abundances were higher for several V-type ATP synthase/ATPase subunits, suggesting the generation of proton gradients in the extrahaustorial space. Other haustoria-associated proteins included secreted or membrane proteins such as a PIP2 aquaporin, an early nodulin-like protein 9, an aspartate protease and other proteases, a lipase, and a lipid transfer protein, all of which are potential modulators of immunity, or the targets of pathogen effectors. Moreover, the ER BIP-like HSP70, may link ER stress responses and the idea of ER-like properties previously attributed to the extrahaustorial membrane. This initial investigation exploring the barley proteomes of Blumeria-infected tissues and haustoria, associated with a transient gene silencing approach, is invaluable to gain first insight of key players of resistance and susceptibility.
Highlights
Powdery mildews cause diseases in numerous plant hosts, including major crops such as cereals, grapevine, strawberries, or cucurbits, to mention a few (Takamatsu, 2013)
Haustoria-enrichment steps were kept to a minimum to avoid damaging the fragile structures, since it was observed that additional steps led to a drastic decrease of intact haustoria
With the use of the workflow presented in this study, candidate gene products that are putatively toxic to the pathogen or that are modulating plant immunity or susceptibility, such as the protein 5 (PR5) isoform TLP 5 (TLP5) or MLO1, can be validated by functional genomics with an in planta Transient-Induced Gene Silencing (TIGS) assay adapted from existing protocols (Sun et al, 2005; Sun et al, 2007; Dinç et al, 2011), exploiting the delivery of short antisense gene-specific phosphorothioate modified oligodeoxriboynucleotides (PTOs)
Summary
Powdery mildews cause diseases in numerous plant hosts, including major crops such as cereals, grapevine, strawberries, or cucurbits, to mention a few (Takamatsu, 2013). Powdery mildews are only able to grow on living plants and typically exhibit a narrow host range (Takamatsu, 2013). Barley and wheat are hosts to Blumeria graminis f. Blumeria and Golovinomyces orontii (Go), which is able to infect Arabidopsis, are the most studied plant-powdery mildew pathosystems (Bindschedler et al, 2016; Kuhn et al, 2016; Bourras et al, 2018). The availability of the barley and Bgh genomes allows for large-scale omics analysis and functional genomics studies (Spanu et al, 2010; Mascher et al, 2017; Frantzeskakis et al, 2018)
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