Yadav, Rashmi

Abstract Phytoplasma diseases are threat to sesame and its wild relatives, but information on their occurrence in exotic Sesamum species is limited. During field evaluation, Sesamum angolense , S. angustifolium , and S. latifolium exhibited characteristic phyllody and witches' broom symptoms, including virescence, leafy floral organs, polysepalous calyx, polypetalous corolla, flattened stamens, shortened internodes, excessive shoot proliferation, and leaf twisting and curling. Molecular detection using universal phytoplasma primers P1/P7 and tuf gene-specific primers fTufAy/rTufAy amplified products of approximately 1.8 kb and 940 bp, respectively, from symptomatic plants. Sequence analysis of the 16S rRNA and tuf genes revealed 99–100% nucleotide identity with members of the 'Candidatus Phytoplasma asteris ' group. Phylogenetic reconstruction based on both loci consistently assigned the isolates to the 16SrI-B subgroup of 'Ca. Phytoplasma asteris'. To the best of our knowledge, this is the first report of phytoplasma infection in S. angolense , S. angustifolium , and S. latifolium , characterized at the strain level using both 16S rRNA and tuf gene sequences. The findings expand the known host range of 16SrI-B phytoplasmas and demonstrate that these wild Sesamum species, which are valuable components of the tertiary gene pool of cultivated sesame, can serve as natural reservoirs of phytoplasma inoculum.

A field investigation was conducted during the winter seasons of 2021–22 and 2022–23 at the Jawaharlal Nehru Krishi Vishwa Vidyalaya (JNKVV), Jabalpur, Central India, to identify and characterize the phytoplasma strains associated with niger (var. JNC6) and sesame (var. RT315) exhibiting severe phyllody symptoms. Disease incidence ranged from 0-3%, and 3 to 15% were recorded in niger and sesame crops during the study period. Nested PCR assays using universal phytoplasma primer pairs P1/P7 followed by R16F2n/R16R2 consistently amplified ~1.25 kb fragments of the 16S rRNA gene from both the symptomatic plants, confirming phytoplasma association. Additional amplification of phytoplasma-specific sec A (~600 bp) and sec Y (~1.7 kb) gene fragments further validated the phytoplasma infection in both crops. Two predominant leafhopper species, Amrasca biguttula and Orosius albicinctus , colonizing and feeding niger and sesame fields were identified. Notably, only Amrasca biguttula was tested positive for phytoplasma using the similar PCR assays mentioned above, implicating it as a putative vector. Sequence identity, phylogenetic analysis, and in silico RFLP profiling of 16S rRNA, sec A, and sec Y gene sequences from both the symptomatic plants and leafhoppers confirmed the presence of a ‘ Ca. P. asiaticum’ related strain (16SrII-C subgroup). This study represents the first global report of 16SrII-C subgroup phytoplasma infection in niger, highlighting a new host record. The detection of an identical phytoplasma strain in niger, sesame, and Amrasca biguttula suggests a possible epidemiological link and underscores the role of these natural hosts and the leafhopper in the dissemination of ‘ Ca. P. asiaticum’-related phytoplasma strains in Central India.