4.6 Article

The Fungal Effector Mlp37347 Alters Plasmodesmata Fluxes and Enhances Susceptibility to Pathogen

Journal

MICROORGANISMS
Volume 9, Issue 6, Pages -

Publisher

MDPI
DOI: 10.3390/microorganisms9061232

Keywords

Melampsora larici-populina; effector; Mlp37347; plasmodesmata; glutamate decarboxylase

Categories

Funding

  1. Natural Sciences and Engineering Research Council of Canada (NSERC)
  2. Tier-II Canada Research Chair
  3. Fonds de Recherche du Quebec sur la Nature et les Technologies (FRQNT-PBEEE)
  4. Mitacs Globalink Research Awards

Ask authors/readers for more resources

The study found that the effector Mlp37347 mainly accumulates at plasmodesmata during infection, promoting parasitic growth by increasing plasmodesmatal flux and reducing callose deposition.
Melampsora larici-populina (Mlp) is a devastating pathogen of poplar trees, causing the defoliating poplar leaf rust disease. Genomic studies have revealed that Mlp possesses a repertoire of 1184 small secreted proteins (SSPs), some of them being characterized as candidate effectors. However, how they promote virulence is still unclear. This study investigates the candidate effector Mlp37347's role during infection. We developed a stable Arabidopsis transgenic line expressing Mlp37347 tagged with the green fluorescent protein (GFP). We found that the effector accumulated exclusively at plasmodesmata (PD). Moreover, the presence of the effector at plasmodesmata favors enhanced plasmodesmatal flux and reduced callose deposition. Transcriptome profiling and a gene ontology (GO) analysis of transgenic Arabidopsis plants expressing the effector revealed that the genes involved in glucan catabolic processes are up-regulated. This effector has previously been shown to interact with glutamate decarboxylase 1 (GAD1), and in silico docking analysis supported the strong binding between Mlp37347 and GAD1 in this study. In infection assays, the effector promoted Hyalonoperospora arabidopsidis growth but not bacterial growth. Our investigation suggests that the effector Mlp37347 targets PD in host cells and promotes parasitic growth.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available