Mohammad Mahbubul Haque, Gobinda Chandra Das, Md Mostofa Faysal, Muhammed Ali Hossain, Marjana Haque, Sifat Miah, Jannatul Farthouse, Mashukur Rahman, Md Nazmul Hasan Mehedi
{"title":"PCR-based detection technique and gamma irradiation strategies for managing <i>Ralstonia solanacearum</i>-induced brown rot of potato.","authors":"Mohammad Mahbubul Haque, Gobinda Chandra Das, Md Mostofa Faysal, Muhammed Ali Hossain, Marjana Haque, Sifat Miah, Jannatul Farthouse, Mashukur Rahman, Md Nazmul Hasan Mehedi","doi":"10.1080/09553002.2025.2451630","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>The study focused on developing a rapid PCR-based detection method and employing gamma irradiation techniques to manage <i>Ralstonia solanacearum</i>, aiming to produce brown rot-free export-quality potatoes. This initiative seeks to enhance potato exports from Bangladesh.</p><p><strong>Materials and methods: </strong>Samples of potato tubers and soil were collected from various commercially significant potato-growing areas, resulting in a total of 168 <i>Ralstonia solanacearum</i> isolates from potato tubers and soil across 12 regions. The detection of <i>R. solanacearum</i> in the enriched tuber extract and soil were conducted using the primer pairs (PS-1, PS-2) and (759, 760). For the gamma irradiation experiment, petri dishes containing <i>R. solanacearum</i> cultures were subjected to different doses of gamma rays at the Bangladesh Institute of Nuclear Agriculture using a <sup>60</sup>Co source. The irradiation doses applied to the samples were 0-6.0KGy.</p><p><strong>Results: </strong>Morphological identification based on pink/light red colonies on TTC medium was confirmed <i>R. solanacearum</i> in 148 isolates. PCR using species-specific primers (PS-1/PS-2) and (759, 760) verified 26 isolates (14 tubers, 12 soil), producing 553 bp and 281 bp fragments in latently infected tubers and soil samples respectively. Gamma irradiation at 2.5 kGy damaged <i>R. solanacearum's</i> DNA and cells, preventing brown rot, while higher doses eliminated it entirely. This offers a promising strategy to enhance safety of stored potatoes, potentially mitigating economic losses from this quarantine pathogen.</p><p><strong>Conclusion: </strong>The study developed a PCR detection method and gamma irradiation techniques to manage <i>R. solanacearum</i>, enhancing the export quality of potatoes.</p>","PeriodicalId":94057,"journal":{"name":"International journal of radiation biology","volume":" ","pages":"1-9"},"PeriodicalIF":0.0000,"publicationDate":"2025-01-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International journal of radiation biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/09553002.2025.2451630","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Purpose: The study focused on developing a rapid PCR-based detection method and employing gamma irradiation techniques to manage Ralstonia solanacearum, aiming to produce brown rot-free export-quality potatoes. This initiative seeks to enhance potato exports from Bangladesh.
Materials and methods: Samples of potato tubers and soil were collected from various commercially significant potato-growing areas, resulting in a total of 168 Ralstonia solanacearum isolates from potato tubers and soil across 12 regions. The detection of R. solanacearum in the enriched tuber extract and soil were conducted using the primer pairs (PS-1, PS-2) and (759, 760). For the gamma irradiation experiment, petri dishes containing R. solanacearum cultures were subjected to different doses of gamma rays at the Bangladesh Institute of Nuclear Agriculture using a 60Co source. The irradiation doses applied to the samples were 0-6.0KGy.
Results: Morphological identification based on pink/light red colonies on TTC medium was confirmed R. solanacearum in 148 isolates. PCR using species-specific primers (PS-1/PS-2) and (759, 760) verified 26 isolates (14 tubers, 12 soil), producing 553 bp and 281 bp fragments in latently infected tubers and soil samples respectively. Gamma irradiation at 2.5 kGy damaged R. solanacearum's DNA and cells, preventing brown rot, while higher doses eliminated it entirely. This offers a promising strategy to enhance safety of stored potatoes, potentially mitigating economic losses from this quarantine pathogen.
Conclusion: The study developed a PCR detection method and gamma irradiation techniques to manage R. solanacearum, enhancing the export quality of potatoes.