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ArticleCurrent microbiology2025

Molecular Characterization of Yellow Mosaic Disease Causing Begomoviruses in Pigeonpea (Cajanus cajan L.) from Three Agro-ecological Zones of India.

Mohammad Akram, Deepender Kumar, Sonu Saurav, Moly Saxena, Deep Ratna Saxena, Naimuddin Kamaal, Girish Prasad Dixit

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Article in Current microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Mohammad AkramDivision of Crop Protection, ICAR-Indian Institute of Pulses Research, Kanpur, 208024, India.
Deepender KumarDivision of Crop Protection, ICAR-Indian Institute of Pulses Research, Kanpur, 208024, India. deependerkr@gmail.com.ORCID http://orcid.org/0000-0003-3139-2855
Sonu SauravDepartment of Plant Pathology, R.A.K. College of Agriculture, Sehore, 466001, India.
Moly SaxenaDepartment of Plant Pathology, R.A.K. College of Agriculture, Sehore, 466001, India.
Deep Ratna SaxenaDepartment of Plant Pathology, R.A.K. College of Agriculture, Sehore, 466001, India.
Naimuddin KamaalDivision of Crop Protection, ICAR-Indian Institute of Pulses Research, Kanpur, 208024, India.
Girish Prasad DixitICAR-Indian Institute of Pulses Research, Kanpur, 208024, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pigeonpea (Cajanus cajan L.) plants exhibiting symptoms of yellow mosaic disease (YMD) were collected in winter 2023 from multiple agricultural fields of Kanpur, Sehore, and Madhubani, representing three different agro-ecological zones in India. The recorded disease incidence ranged from 3 to 5%, 1 to 4%, and 12 to 20% in these zones, respectively. This study aimed to identify and characterize the causal agent, suspected to be a begomovirus, an emerging plant pathogen of pigeonpea causing YMD. Total DNA was extracted from 28 YMD-affected leaf samples and subjected to rolling circle amplification for PCR-based virus detection. Of all the tested samples, one tested positive for mungbean yellow mosaic virus (MYMV), while the remaining tested positive for mungbean yellow mosaic India virus (MYMIV). Subsequently, PCR-based amplification and sequencing of the full-length DNA-A and DNA-B components were conducted. BLASTn analysis revealed that the assembled sequences of the DNA-A and DNA-B components had the highest nucleotide identity with MYMIV (DNA-A: 97-99%, DNA-B: 95-97%) and MYMV (DNA-A: 99%, DNA-B: 98%). Phylogenetic analysis supported these findings. Additionally, the DNA-A and DNA-B components obtained from each sample were found to be cognate, with over 92% similarity in their common region. Thus, the cognate DNA components constituted the isolates of MYMIV and MYMV identified from pigeonpea. The identified isolates exhibited the typical genome organization of an Old World bipartite begomovirus, with no recombination events detected. This study reports, for the first time, the complete annotated genomes of MYMIV from Sehore and Madhubani, as well as MYMIV and MYMV from Kanpur, infecting pigeonpea.

Indexed as

BegomovirusCajanusPlant DiseasesDNA, ViralGenome, ViralIndiaPhylogenyPlant LeavesDNA, Viral

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.