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Identification and expression analysis of pathogenicity-related genes of Rhizoctonia solani anastomosis groups infecting rice.
Prashantha, S T; Bashyal, B M; Krishnan, S Gopala; Dubey, Himanshu; Solanke, Amolkumar U; Prakash, G; Aggarwal, Rashmi.
Affiliation
  • Prashantha ST; Division of Plant Pathology, ICAR-Indian Agricultural Research Institute, New Delhi, 110012 India.
  • Bashyal BM; Division of Plant Pathology, ICAR-Indian Agricultural Research Institute, New Delhi, 110012 India.
  • Krishnan SG; Division of Genetics, ICAR-Indian Agricultural Research Institute, New Delhi, 110012 India.
  • Dubey H; ICAR-National Institute for Plant Biotechnology, IARI, New Delhi, 110012 India.
  • Solanke AU; Present Address: Seribiotechnology Research Laboratory (SBRL), Central Silk Board, Bangalore, 560 068 India.
  • Prakash G; ICAR-National Institute for Plant Biotechnology, IARI, New Delhi, 110012 India.
  • Aggarwal R; Division of Plant Pathology, ICAR-Indian Agricultural Research Institute, New Delhi, 110012 India.
3 Biotech ; 11(8): 394, 2021 Aug.
Article in En | MEDLINE | ID: mdl-34458063
Sheath blight disease caused by Rhizoctonia solani Kuhn (teleomorph; Thanatephorus cucumeris) is a major constraint in rice production. Among the different anastomosis groups (AGs) of Rhizoctonia solani, AG1-IA causes sheath blight of rice, which induce necrotic lesions on leaf sheaths of the infected plants. Several reports contradict the host specificity of anastomosis groups in Rhizoctonia solani. There is lack of information on the pathogenicity genes of these Rhizoctonia solani anastomosis groups during sheath blight infection in rice. In the present study, Rhizoctonia solani isolates collected from diverse rice growing regions of India were screened for anastomosis groups and two groups namely, AG1-IA, AG2-2 were identified. Accordingly, comparative studies were made with AG1-IA (GenBank ID: 16,395) and AG2-2 (GenBank ID: 2,318,768) group sequences, which enabled the identification of specific gene clusters (119 in AG1-IA and 604 in AG2-2) belonging to these groups. Pathogen Host Interaction (PHI) blast with these specific gene clusters could further identify genes involved in host pathogen interaction (38 in AG1_IA and 150 in AG2-2), which were shortlisted for qRT-PCR validation based on qcov cutoff values representing different phenotypic categories of PHI blast. Expression analysis-based validation in sheath blight susceptible (Pusa Basmati 1) and resistant (Pusa 1908-13-12-5) rice genotypes showed that most of the genes expressed significantly higher in the susceptible variety Pusa Basmati 1. The genes like inorganic phosphate transporter (AG1_IPT), Bromodomain containing protein (AG1_BrD), Aldehyde dehydrogenase (AG1_AldD), AMP binding domain (AG1_AMP) and Heme peroxidase (AG1_HmPr) were upregulated in the susceptible genotype, PB 1 at 72hpi compared to Pusa 1908-13-12-5. Among these, inorganic phosphate transporter (AG1_IPT), Bromodomain containing protein (AG1_BrD) and Heme peroxidase (AG1_HmPr) were specific to Rhizoctonia solani AG1-IA. Through the present study, we could demonstrate the AG1-IA-specific interactions of Rhizoctonia solani causing sheath blight disease of rice, which is a step forward in understanding the specificity of Rhizoctonia solani with reference to sheath blight disease of rice. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s13205-021-02934-1.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Diagnostic_studies Language: En Journal: 3 Biotech Year: 2021 Document type: Article Country of publication: Germany

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Diagnostic_studies Language: En Journal: 3 Biotech Year: 2021 Document type: Article Country of publication: Germany