Indian Journal of Genetics and Plant Breeding (The)
SCOPUSWeb of Science
  • Year: 2024
  • Volume: 84
  • Issue: 2

Identification of cowpea [Vigna unguiculata (L.) Walp.] germplasm accessions resistant to yellow mosaic disease

  • Author:
  • G. J. Abhishek, Kuldeep Tripathi, Susheel K. Sharma1, B. Parameshwari, Nitika Gupta1, Damini Diksha1, Amalendu Ghosh1, Sunil Archak, Dhammaprakash P. Wankhede, D.D. Deepika, T. Danakumar3, K. Kalaiponmani, Vignesh Muthusamy3, V. Celia Chalam1,*
  • Total Page Count: 8
  • Page Number: 258 to 265

1Division of Plant Pathology, ICAR-Indian Agricultural Research Institute, New Delhi, 110 012, India

3Division of Genetic and Plant Breeding, ICAR-Indian Agricultural Research Institute, New Delhi, 110 012, India

Division of Plant Genetic Resources, ICAR- National Bureau of Plant Genetic Resources, New Delhi, 110 012, India

*Corresponding Author: V. Celia Chalam, ICAR-National Bureau of Plant Genetic Resources, New Delhi, 110012, India, E-Mail: celia.chalam@icar.gov.in, mailcelia@gmail.com

Online published on 2 July, 2025.

Abstract

Yellow mosaic disease (YMD) of cowpea, predominantly caused by mungbean yellow mosaic India virus (MYMIV) and mungbean yellow mosaic virus (MYMV) is a major constraint to the production of cowpea (Vigna unguiculata L.) in India resulting in significant yield reductions. The present study extensively evaluated 1127 cowpea germplasm accessions from the National Gene Bank of India, New Delhi, at two hotspot locations (Hyderabad and Delhi) for their response to YMD. About 181 accessions showed no symptoms in field screening at both locations and were considered putatively resistant. A set of the best 100 out of 181 was selected for further confirmation of resistance to MYMIV through whitefly-mediated screening along with 40 accessions known to be susceptible to YMD. The results of whitefly-mediated transmission confirmed MYMIV resistance in 20 accessions with a disease score of zero. Further, the YMD-associated Begomovirus was characterized using rolling circle amplification coupled with sequencing of the full DNA-A genome of MYMIV, which shared an identity of 99.02% with the MYMIV isolate infecting cowpea in Pakistan. The 20 cowpea accessions identified as novel resistant sources to MYMIV in the present study could be used for mapping resistance genes and as donors in resistance breeding for yellow mosaic disease.

Keywords

Cowpea germplasm, Evaluation, Begomovirus, Mungbean yellow mosaic India virus