Optimisation of Sporosori Purification and Protein Extraction Techniques for the Biotrophic Protozoan Plant Pathogen <i>Spongospora subterranea</i>
<i>Spongospora subterranea</i> is a soil-borne plant pathogen responsible for the economically significant root and powdery scab diseases of potato. However, the obligate biotrophic nature of <i>S. subterranea</i> has made the detailed study of the pathogen problematic. Here,...
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doaj-7d069d21b21443fbaa897323441bcd8e2020-11-25T02:41:32ZengMDPI AGMolecules1420-30492020-07-01253109310910.3390/molecules25143109Optimisation of Sporosori Purification and Protein Extraction Techniques for the Biotrophic Protozoan Plant Pathogen <i>Spongospora subterranea</i>Sadegh Balotf0Richard Wilson1Robert S. Tegg2David S. Nichols3Calum R. Wilson4Tasmanian Institute of Agriculture, New Town Research Laboratories, University of Tasmania, New Town, Tasmania 7008, AustraliaCentral Science Laboratory, University of Tasmania, Hobart, Tasmania 7001, AustraliaTasmanian Institute of Agriculture, New Town Research Laboratories, University of Tasmania, New Town, Tasmania 7008, AustraliaCentral Science Laboratory, University of Tasmania, Hobart, Tasmania 7001, AustraliaTasmanian Institute of Agriculture, New Town Research Laboratories, University of Tasmania, New Town, Tasmania 7008, Australia<i>Spongospora subterranea</i> is a soil-borne plant pathogen responsible for the economically significant root and powdery scab diseases of potato. However, the obligate biotrophic nature of <i>S. subterranea</i> has made the detailed study of the pathogen problematic. Here, we first compared the benefits of sporosori partial purification utilizing Ludox<sup>®</sup> gradient centrifugation. We then undertook optimization efforts for protein isolation comparing the use of a urea buffer followed by single-pot solid-phase-enhanced sample preparation (SP3) and a sodium dodecyl sulphate (SDS) buffer followed by suspension-trapping (S-Trap). Label-free, quantitative proteomics was then used to evaluate the efficiency of the sporosori purification and the protein preparation methods. The purification protocol produced a highly purified suspension of <i>S. subterranea</i> sporosori without affecting the viability of the spores. The results indicated that the use of a combination of SDS and S-Trap for sample clean-up and digestion obtained a significantly higher number of identified proteins compared to using urea and SP3, with 218 and 652 proteins identified using the SP3 and S-Trap methods, respectively. The analysis of proteins by mass spectrometry showed that the number of identified proteins increased by approximately 40% after the purification of spores by Ludox<sup>®</sup>. These results suggested a potential use of the described spore purification and protein preparation methods for the proteomics study of obligate biotrophic pathogens such as <i>S. subterranea</i>.https://www.mdpi.com/1420-3049/25/14/3109<i>Spongospora subterranea</i>sporosoridensity gradient centrifugationLudox<sup>®</sup>proteomicsS-Trap |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Sadegh Balotf Richard Wilson Robert S. Tegg David S. Nichols Calum R. Wilson |
spellingShingle |
Sadegh Balotf Richard Wilson Robert S. Tegg David S. Nichols Calum R. Wilson Optimisation of Sporosori Purification and Protein Extraction Techniques for the Biotrophic Protozoan Plant Pathogen <i>Spongospora subterranea</i> Molecules <i>Spongospora subterranea</i> sporosori density gradient centrifugation Ludox<sup>®</sup> proteomics S-Trap |
author_facet |
Sadegh Balotf Richard Wilson Robert S. Tegg David S. Nichols Calum R. Wilson |
author_sort |
Sadegh Balotf |
title |
Optimisation of Sporosori Purification and Protein Extraction Techniques for the Biotrophic Protozoan Plant Pathogen <i>Spongospora subterranea</i> |
title_short |
Optimisation of Sporosori Purification and Protein Extraction Techniques for the Biotrophic Protozoan Plant Pathogen <i>Spongospora subterranea</i> |
title_full |
Optimisation of Sporosori Purification and Protein Extraction Techniques for the Biotrophic Protozoan Plant Pathogen <i>Spongospora subterranea</i> |
title_fullStr |
Optimisation of Sporosori Purification and Protein Extraction Techniques for the Biotrophic Protozoan Plant Pathogen <i>Spongospora subterranea</i> |
title_full_unstemmed |
Optimisation of Sporosori Purification and Protein Extraction Techniques for the Biotrophic Protozoan Plant Pathogen <i>Spongospora subterranea</i> |
title_sort |
optimisation of sporosori purification and protein extraction techniques for the biotrophic protozoan plant pathogen <i>spongospora subterranea</i> |
publisher |
MDPI AG |
series |
Molecules |
issn |
1420-3049 |
publishDate |
2020-07-01 |
description |
<i>Spongospora subterranea</i> is a soil-borne plant pathogen responsible for the economically significant root and powdery scab diseases of potato. However, the obligate biotrophic nature of <i>S. subterranea</i> has made the detailed study of the pathogen problematic. Here, we first compared the benefits of sporosori partial purification utilizing Ludox<sup>®</sup> gradient centrifugation. We then undertook optimization efforts for protein isolation comparing the use of a urea buffer followed by single-pot solid-phase-enhanced sample preparation (SP3) and a sodium dodecyl sulphate (SDS) buffer followed by suspension-trapping (S-Trap). Label-free, quantitative proteomics was then used to evaluate the efficiency of the sporosori purification and the protein preparation methods. The purification protocol produced a highly purified suspension of <i>S. subterranea</i> sporosori without affecting the viability of the spores. The results indicated that the use of a combination of SDS and S-Trap for sample clean-up and digestion obtained a significantly higher number of identified proteins compared to using urea and SP3, with 218 and 652 proteins identified using the SP3 and S-Trap methods, respectively. The analysis of proteins by mass spectrometry showed that the number of identified proteins increased by approximately 40% after the purification of spores by Ludox<sup>®</sup>. These results suggested a potential use of the described spore purification and protein preparation methods for the proteomics study of obligate biotrophic pathogens such as <i>S. subterranea</i>. |
topic |
<i>Spongospora subterranea</i> sporosori density gradient centrifugation Ludox<sup>®</sup> proteomics S-Trap |
url |
https://www.mdpi.com/1420-3049/25/14/3109 |
work_keys_str_mv |
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