| Literature DB >> 31667538 |
Muhammad Adnan1,2, Wenqin Fang1,2, Peng Sun1,2, Yangling Zheng1,2, Yakubu Saddeeq Abubakar3, Jing Zhang1,2, Yi Lou1,2, Wenhui Zheng4,5,6, Guo-Dong Lu7,8.
Abstract
SNAREs (soluble N-ethylmaleimide-sensitive factor attachment protein receptors) facilitate intracellular vesicle trafficking and membrane fusion in eukaryotic cells, and play a vital role in growth, development and pathogenicity of phytopathogens. Fusarium head blight (FHB) caused by F. graminearum is one of the most devastating diseases of wheat and barley worldwide. Sec22 is a member of the SNARE family of proteins and its homologues have been shown to have diverse biological roles in different organisms. However, the functions of this protein in the development and pathogenesis of F. graminearum are currently unknown. In this study, we employed integrated biochemical, microbiological and molecular genetic approaches to investigate the roles of FgSec22 in F. graminearum. Our data reveal that this SNARE protein is localized to endoplasmic reticulum (ER) and is indispensable for normal conidiation, conidial morphology and pathogenesis of this phytopathogenic fungus. Our biochemical assay of deoxynivalenol (DON) reveals the active involvement of this protein in the production of this mycotoxin in F. graminearum. This has further been confirmed by qRT-PCR analyses of trichothecene (TRI) genes' expression where the ΔFgsec22 deletion mutant demonstrated a significant down-regulation of these genes in comparison to the wild-type PH-1. Unlike the wild-type and the complemented strain, the mutant strain presents a remarkable defect in colony formation which reflects the critical role it plays in vegetative growth. Collectively, our data support that the SNARE protein FgSec22 is required for vegetative growth, pathogenesis and DON biosynthesis in F. graminearum.Entities:
Keywords: Cell wall integrity; Fusarium head blight; Membrane fusion; Phenotypic characterization; Vesicle trafficking
Year: 2019 PMID: 31667538 DOI: 10.1007/s00294-019-01037-y
Source DB: PubMed Journal: Curr Genet ISSN: 0172-8083 Impact factor: 3.886