Intact spore MALDI-TOF mass spectrometry and proteomic analysis of Puccinia pathogenic fungi
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
27267623
DOI
10.1016/j.bbapap.2016.06.002
PII: S1570-9639(16)30111-X
Knihovny.cz E-zdroje
- Klíčová slova
- Biotyping, Intact cell/spore mass spectrometry, MALDI-TOF, Pathotype, Protein identification, Rust,
- MeSH
- acetonitrily chemie MeSH
- Basidiomycota chemie MeSH
- fungální proteiny genetika izolace a purifikace MeSH
- histony genetika izolace a purifikace MeSH
- kyselina trifluoroctová chemie MeSH
- kyseliny kumarové chemie MeSH
- nemoci rostlin mikrobiologie MeSH
- proteomika MeSH
- pšenice mikrobiologie MeSH
- ribozomální proteiny genetika izolace a purifikace MeSH
- rozpouštědla chemie MeSH
- spektrometrie hmotnostní - ionizace laserem za účasti matrice MeSH
- spory hub chemie MeSH
- zemědělské plodiny mikrobiologie MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- acetonitrile MeSH Prohlížeč
- acetonitrily MeSH
- ferulic acid MeSH Prohlížeč
- fungální proteiny MeSH
- histony MeSH
- kyselina trifluoroctová MeSH
- kyseliny kumarové MeSH
- ribozomální proteiny MeSH
- rozpouštědla MeSH
- sinapinic acid MeSH Prohlížeč
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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