Abstract

Rhizoctonia solani AG1-IA (Thandfephorus cucumeris teleomorph) is the causative agent of rice sheath blight in Chinese paddy fields. Due to the importance of the disease and the lack of comprehensive information on the genetic structure of the fungus populations, 25 isolates collected from Hubei, Sichuan, Anhui, and Jiangsu provinces, and southern China's Yangtze River basin were examined for morphological characteristics, growth rate, and genetic diversity of this pathogen. The anastomosis group determination test results showed that all isolates belong to the AG1-IA anastomosis group. To quickly diagnose and confirm the anastomosis group of isolates, ten isolates along with AG1-IA and AGA standard isolates were examined by specific primers AG1-IA. A 256bp band was amplified in all of them. The results of the growth velocity study divided the isolates into two groups' fast growth (68% of isolates) and slow growth (32% of isolates). The genetic diversity of 25 isolates was assessed using the RAPD marker. Among the 20 primers, bands from seven primers ranging from 250 to 5,000bp were performed using the Jaccard similarity coefficient and UPGMA method by data cluster analysis of NTSYS-pc software. The cluster analysis results divided the isolates into two groups with a similarity level of 36%, which corresponded to the grouping of isolates into two groups of fast growth and slow growth. At the level of 80% similarity, the isolates were divided into 23 groups, which indicate the high genetic diversity of these isolates. The results of the molecular analysis showed that isolates belonging to a geographical area do not necessarily have a genetic affinity. This study performed rapid detection of R. solani AG1-IA using specific primers AG1-IA, and evaluation of genetic diversity of rice sheath blight isolates was performed by RAPD marker in this study.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.