ArticlePLoS pathogens2010
Chitin synthases from Saprolegnia are involved in tip growth and represent a potential target for anti-oomycete drugs.
Article in PLoS pathogens, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.
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33 citing papers in PubMed, 88 citations in OpenAlex.
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- The MIT domain of chitin synthase 1 from the oomyceteBiochemistry and biophysics reports · 2022Article
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- Organize, Don't Agonize: Strategic Success ofMicroorganisms · 2020Review
- Identification of Growth Inhibitors of the Fish PathogenFrontiers in microbiology · 2020Article
- Bioimaging structural signatures of the oomycete pathogen Sclerospora graminicola in pearl millet using different microscopic techniques.Scientific reports · 2019Article
- Colonization of Different Grapevine Tissues byFrontiers in plant science · 2019Article
- Identification and Characterization of the Chitin Synthase Genes From the Fish PathogenFrontiers in microbiology · 2019Article
- Binding of theThe Plant cell · 2019Article
- Large-scale additive manufacturing with bioinspired cellulosic materials.Scientific reports · 2018Article
- Biocontrol of Orchid-pathogenic Mold,Mycobiology · 2018Article
- Structural characterization of a putative chitin synthase gene in Phytophthora spp. and analysis of its transcriptional activity during pathogenesis on potato and soybean plants.Current genetics · 2017Article
- Synthesis and Evaluation of Novel Oxyalkylated Derivatives of 2',4'-Dihydroxychalcone as Anti-Oomycete Agents against Bronopol Resistant Strains of Saprolegnia sp.International journal of molecular sciences · 2016Article
- Theobroma cacao L. pathogenesis-related gene tandem array members show diverse expression dynamics in response to pathogen colonization.BMC genomics · 2016Article
- PsHint1, associated with the G-protein α subunit PsGPA1, is required for the chemotaxis and pathogenicity of Phytophthora sojae.Molecular plant pathology · 2016Article
- Oomycete interactions with plants: infection strategies and resistance principles.Microbiology and molecular biology reviews : MMBR · 2015Review
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Authors and funding
6 authors at 4 institutions in 2 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Oomycetes represent some of the most devastating plant and animal pathogens. Typical examples are Phytophthora infestans, which causes potato and tomato late blight, and Saprolegnia parasitica, responsible for fish diseases. Despite the economical and environmental importance of oomycete diseases, their control is difficult, particularly in the aquaculture industry. Carbohydrate synthases are vital for hyphal growth and represent interesting targets for tackling the pathogens. The existence of 2 different chitin synthase genes (SmChs1 and SmChs2) in Saprolegnia monoica was demonstrated using bioinformatics and molecular biology approaches. The function of SmCHS2 was unequivocally demonstrated by showing its catalytic activity in vitro after expression in Pichia pastoris. The recombinant SmCHS1 protein did not exhibit any activity in vitro, suggesting that it requires other partners or effectors to be active, or that it is involved in a different process than chitin biosynthesis. Both proteins contained N-terminal Microtubule Interacting and Trafficking domains, which have never been reported in any other known carbohydrate synthases. These domains are involved in protein recycling by endocytosis. Enzyme kinetics revealed that Saprolegnia chitin synthases are competitively inhibited by nikkomycin Z and quantitative PCR showed that their expression is higher in presence of the inhibitor. The use of nikkomycin Z combined with microscopy showed that chitin synthases are active essentially at the hyphal tips, which burst in the presence of the inhibitor, leading to cell death. S. parasitica was more sensitive to nikkomycin Z than S. monoica. In conclusion, chitin synthases with species-specific characteristics are involved in tip growth in Saprolegnia species and chitin is vital for the micro-organisms despite its very low abundance in the cell walls. Chitin is most likely synthesized transiently at the apex of the cells before cellulose, the major cell wall component in oomycetes. Our results provide important fundamental information on cell wall biogenesis in economically important species, and demonstrate the potential of targeting oomycete chitin synthases for disease control.
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