عنوان المقالة:New Strategy for Inducing Resistance against Bacterial Wilt Disease Using an Avirulent Strain of Ralstonia solanacearum New Strategy for Inducing Resistance against Bacterial Wilt Disease Using an Avirulent Strain of Ralstonia solanacearum
د زياد موسى عبد المعطي | Zeiad Moussa Abd El-Moati | 6770
نوع النشر
مقال علمي
المؤلفون بالعربي
الملخص الانجليزي
Ralstonia solanacearum is one of the globally significant plant pathogens that infect a wide host range of economically important plants. A study was conducted to evaluate the hypothesis that an avirulent strain of R. solanacearum can act as a biocontrol mediator for managing potato bacterial wilt. Virulent R. solanacearum was isolated and identified (GenBank accession number; OP180100). The avirulent strain was obtained from the virulent strain through storage for 3 weeks until the development of deep red colonies. The virulent strain had higher lytic activity than the avirulent strain. Tubers' treatments by the avirulent strain of R. solanacearum, (supernatant, boiled supernatant, and dead cells) significantly reduced plant disease rating and increased the growth, physiological activities, and biomass of potato compared to the untreated, infected control. The major components detected by GC-MS in the supernatant revealed 10.86% palmitic acid (virulent), and 18.03% 1,3-dioxolane, 2,4,5-trimethyl-(avirulent), whereas the major component in the boiled supernatant was 2-hydroxy-gamma-butyrolactone in the virulent (21.17%) and avirulent (27.78%) strains. This is the first research that assessed the influence of boiled supernatant and dead cells of virulent and avirulent R. solanacearum strains in controlling bacterial wilt disease. Additional work is encouraged for further elucidation of such a topic.
تاريخ النشر
10/09/2022
الناشر
microorganisms mdpi
رقم المجلد
رقم العدد
رابط DOI
10.3390/microorganisms10091814
رابط الملف
تحميل (0 مرات التحميل)
رابط خارجي
https://www.mdpi.com/2076-2607/10/9/1814
الكلمات المفتاحية
biological control; bacterial supernatant; defense-related enzymes; GC–MS analysis;
رجوع