Intact spore MALDI-TOF mass spectrometry and proteomic analysis of Puccinia pathogenic fungi
Language English Country Netherlands Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
27267623
DOI
10.1016/j.bbapap.2016.06.002
PII: S1570-9639(16)30111-X
Knihovny.cz E-resources
- Keywords
- Biotyping, Intact cell/spore mass spectrometry, MALDI-TOF, Pathotype, Protein identification, Rust,
- MeSH
- Acetonitriles chemistry MeSH
- Basidiomycota chemistry MeSH
- Fungal Proteins genetics isolation & purification MeSH
- Histones genetics isolation & purification MeSH
- Trifluoroacetic Acid chemistry MeSH
- Coumaric Acids chemistry MeSH
- Plant Diseases microbiology MeSH
- Proteomics MeSH
- Triticum microbiology MeSH
- Ribosomal Proteins genetics isolation & purification MeSH
- Solvents chemistry MeSH
- Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization MeSH
- Spores, Fungal chemistry MeSH
- Crops, Agricultural microbiology MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- acetonitrile MeSH Browser
- Acetonitriles MeSH
- ferulic acid MeSH Browser
- Fungal Proteins MeSH
- Histones MeSH
- Trifluoroacetic Acid MeSH
- Coumaric Acids MeSH
- Ribosomal Proteins MeSH
- Solvents MeSH
- sinapinic acid MeSH Browser
The aim of this work was to develop a method for the identification of pathogens causing rust diseases of crops using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) of intact cells or spores (IC/IS). All optimizations were performed with Puccinia triticina, the causal agent of wheat leaf rust. Experiments included selection of washing solvents for spores, finding of an optimal concentration of spores in suspension and the most suitable matrix system as well as an evaluation of different sample preparation techniques. The best results were obtained when the spores were washed with acetonitrile/0.1% (v/v) trifluoroacetic acid, 7:3, v/v. A mixture of ferulic and sinapinic acids (5:15mgml(-1)) dissolved in acetonitrile/2.5% (v/v) trifluoroacetic acid, 7:3, v/v, was found optimal for the deposition of samples (50μg spores per μl) by two-layer volume technique. The optimized protocol was subsequently applied to other Puccinia species (Puccinia graminis, Puccinia striiformis and Puccinia coronata). Together with the use of the software BIOSPEAN, not only different species but also various pathotypes of the same species, which differ in their virulence, could be discriminated. There were 108 and 29 proteins identified from P. striiformis and P. graminis spores, respectively, after an acidic extraction in the matrix solvent mimicking the sample preparation for MALDI. Besides the presence of ribosomal proteins, histones, regulatory proteins and enzymes, also extracellular proteins participating in the pathogenesis were found. Finally, for both species, several proteins were assigned to signals in typical mass spectrometric profiles and suggested as diagnostic markers.
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