Grain legumes remain important to meet the projected targets relating to food and nutritional security worldwide. The complementation of cereal-based food with grain legumes is a vegetarian diet with high-quality protein.However, the performance of these crops is severely influenced by a number of biotic and abiotic stresses, of which pests and pathogens remain the crucial affecting plants at different growth stages. Chemical pesticides are mainly employed across the world for management of pests and pathogens. The risk associated with the environmental pollution and health hazards to man, plants, domestic animals, and wild life makes these pesticides ecologically unacceptable. Also, major damage caused by pests of grain legumes are systemic in nature, and their management through chemicals often yields unsatisfactory outcome. This has led to increasing shift in the attention of scientific community towards eco-friendly and safer technologies for pest management in legumes. Sustainable protection demands implementation of strategies that rely upon biological control agents (BCAs) and their formulations. In recent years, such formulations have been promoted to mitigate the pest problem and improving crop yield. This review presents an updated summary on BCAs including the present status of BCA application, mode of actions, and delivery systems under controlled and field conditions to address major pest problems on legume crops.

Begomoviruses are emerging as serious threat to many crops throughout the world particularly in tropical and sub-tropical regions. A leaf curl disease with symptoms typical of infection by many begomoviruses was observed in French bean (Phaseolus vulgaris) at Kanpur, India, during 2010-2012. The disease caused downward leaf curling and made the plants unproductive. The disease was transmitted from infected to healthy plants through whitefly (Bemisia tabaci). The products of five samples digested with EcoRI yielded DNA fragments of about 2.7 kb. The complete sequence of the Fb1 sample comprised 2,741 nucleotides with genome organization typical of begomoviruses having two ORFs in virion-sense and five ORFs in complementary-sense separated by an intergenic region with begomovirus conserved nonanucleotide sequence, TAATATTAC. The complete DNA-A sequence homology was most closely related to Cotton leaf curl Bangalore virus with 80 % nucleotide sequence identity. Based on the demarcation criteria for identifying a begomovirus species, Fb1 is considered as a distinct begomovirus species, named French bean leaf curl virus and designated as FbLCV-[IN:Knp:12]. The complete sequence of associated satellite DNA-β comprises 1,379 nucleotides with single ORF and has 80 % identity with Papaya leaf curl beta satellite. There was no evidence of recombination in DNA-A of FbLCV and associated beta satellite DNA molecule.

A leaf curl disease with symptoms typical of begomoviruses was observed in bean (Phaseolus vulgaris) at the Main Research Farm of the Indian Institute of Pulses Research, Kanpur, India. Infected plants had severe distortion of leaves and the plants were unproductive. PCR indicated the involvement of French bean leaf curl virus (JQ866297), a recently described Begomovirus, and Tomato leaf curl Gujarat virus (ToLCGV). The full‐length genome of ToLCGV associated with leaf curl disease of bean was 2757 nucleotides long and had maximum identity (97–98%) with seven isolates of ToLCGV (AY234383, AF449999, EU573714, GQ994098, AY190290, FR819708, AF413671) and is designated as Tomato leaf curl Gujarat virus‐(IN:Knp:Bean:2013) (KF440686). To the best of our knowledge, this is the first record of ToLCGV infecting a leguminous host, P. vulgaris.

Polymerase chain reaction assays of eight yellow mosaic disease (YMD) affected moth bean samples using specific primers indicated the presence of Mungbean yellow mosaic virus (MYMV), Mungbean yellow mosaic India virus (MYMIV) and Horsegram yellow mosaic virus (HgYMV) in two samples (Mo1 and Mo5) and two of these three viruses in remaining six samples. Sequence data analysis of Mo1 and Mo2 revealed the involvement of multiple DNA‐A and DNA‐B molecules in both samples. Further analysis of DNA‐A and DNA‐B molecules confirmed the presence of three viruses viz., MYMIV, MYMV and HgYMV, in Mo1 and of two MYMV and HgYMV in Mo2 samples. Analysis of common region (CR) sequences of components (DNA‐A and DNA‐B) of each virus indicated >85% nucleotide identity confirming them to be cognate and species integrity. The recombination analysis revealed the presence of a total of six putative recombination events in the viruses under study. In a phylogenetic analysis of DNA‐A sequences of the viruses under study with bipartite legume‐infecting begomoviruses and some selected old and new world begomoviruses, MYMIV, MYMV and HgYMV grouped with respective virus species. Similar grouping and clustering were found in the DNA‐B sequences also. The present study reports infection by HgYMV in moth bean and the association of three viruses (MYMIV, MYMV and HgYMV) with moth bean yellow mosaic disease for the first time. The presence of mixed infection of begomoviruses provides opportunities for the exchange of DNA between the species which may lead to the development of new strain/virus species.

The movement protein (NSm) gene of Groundnut bud necrosis virus (GBNV) isolates from pea, mungbean, cowpea, French bean, tomato and potato collected from different locations of India were compared to study their diversity. The NSm gene sequences of all the GBNV isolates were highly conserved and had only 0–3% diversity in amino acids and 0–10% in nucleotides. Comparison of amino acid sequence of NSm gene of 25 GBNV isolates revealed the presence of many conserved regions. Both ‘D‐motif’ and ‘G‐residue’, the conserved regions of ‘30K superfamily’ of virus movement protein, were present in all the isolates. Clustering of the GBNV isolates does not appear to be based on their place of origin and host plant species.

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An attempt was made to characterize the Phytoplasma in suspected cowpea (Vigna unguiculata L.) samples showing symptoms consisting of bud proliferation and stunting at Experimental Farm, ICAR-NBPGR, New Delhi during Kharif 2020. Associated phytoplasma was characterized based on sequence analysis of target 16S rDNA fragments of 1247 bp amplified from symptomatic samples of cowpea by nested-polymerase chain reaction assay using universal phytoplasma specific primers pairs (P1/P7 and R16F2n/ R16R2). The 16S rDNA sequences understudy shared 98.6% similarity with that of the Candidatus Phytoplasma aurantifolia (GenBank accession: U15442). In phylogenetic analysis, the target 16S rDNA fragment from two samples (Cow-1 and Cow-2) clustered with strains of the 16SrII group of Ca. Phytoplasma aurantifolia. The virtual RFLP pattern showed the highest similarity with the reference pattern of the 16SrII-D subgroup (GenBank accession: Y10097) with a coefficient of 0.97. Since obtained coefficient value is equal to the threshold (0.97) for designating a different strain. Therefore, this phytoplasma infecting cowpea is proposed to be a new strain of Ca. P. aurantifolia as 16SrII-Ysubgroup.

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