S. Pande

Marker-Assisted Backcrossing to Introgress Resistance to Fusarium Wilt Race 1 and Ascochyta Blight in C 214, an Elite Cultivar of Chickpea

Fusarium wilt (FW) and Ascochyta blight (AB) are two major constraints to chickpea (Cicer arietinum L.) production. Therefore, two parallel marker‐assisted backcrossing (MABC) programs by targeting foc1 locus and two quantitative trait loci (QTL) regions, ABQTL‐I and ABQTL‐II, were undertaken to introgress resistance to FW and AB, respectively, in C 214, an elite cultivar of chickpea. In the case of FW, foreground selection (FGS) was conducted with six markers (TR19, TA194, TAA60, GA16, TA110, and TS82) linked to foc1 in the cross C 214 × WR 315 (FW‐resistant). On the other hand, eight markers (TA194, TR58, TS82, GA16, SCY17, TA130, TA2, and GAA47) linked with ABQTL‐I and ABQTL‐II were used in the case of AB by deploying C 214 × ILC 3279 (AB‐resistant) cross. Background selection (BGS) in both crosses was employed with evenly distributed 40 (C 214 × WR 315) to 43 (C 214 × ILC 3279) SSR markers in the chickpea genome to select plant(s) with higher recurrent parent genome (RPG) recovery. By using three backcrosses and three rounds of selfing, 22 BC3F4 lines were generated for C 214 × WR 315 cross and 14 MABC lines for C 214 × ILC 3279 cross. Phenotyping of these lines has identified three resistant lines (with 92.7–95.2% RPG) to race 1 of FW, and seven resistant lines (with 81.7–85.40% RPG) to AB that may be tested for yield and other agronomic traits under multilocation trials for possible release and cultivation.

Ascochyta blight of chickpea (Cicer arietinum L.): a review of biology, pathogenicity, and disease management

Ascochyta blight (AB), caused by Ascochyta rabiei is a major disease of chickpea (Cicer arietinum L.), especially in areas where cool, cloudy, and humid weather persists during the crop season. Several epidemics of AB causing complete yield loss have been reported. The fungus mainly survives between seasons through infected seed and in infected crop debris. Despite extensive pathological and molecular studies, the nature and extent of pathogenic variability in A. rabiei have not been clearly established. Accumulation of phenols, phytoalexins (medicarpin and maackiain), and hydrolytic enzymes has been associated with host-plant resistance (HPR). Seed treatment and foliar application of fungicides are commonly recommended for AB management, but further information on biology and survival of A. rabiei is needed to devise more effective management strategies. Recent studies on inheritance of AB resistance indicate that several quantitative trait loci (QTLs) control resistance. In this paper we review the biology of A. rabiei, HPR, and management options, with an emphasis on future research priorities.

Variation in pathogenicity and cultural characteristics of sorghum isolates of Colletotrichum graminicola in India.

The pathogenicity of nine sorghum isolates of Colletotrichum graminicola from different locations in India was tested on 30 sorghum genotypes in the greenhouse. Based on reaction class and disease severity, six genotypes were identified as susceptible and seven as resistant to all nine isolates of the pathogen. The remaining 17 genotypes exhibited differential responses to the nine isolates. The isolates also varied in their cultural characteristics. These results indicated that the nine isolates were distinct physiologic races (...)

Defining the Transcriptome Assembly and Its Use for Genome Dynamics and Transcriptome Profiling Studies in Pigeonpea (Cajanus cajan L.)

This study reports generation of large-scale genomic resources for pigeonpea, a so-called ‘orphan crop species’ of the semi-arid tropic regions. FLX/454 sequencing carried out on a normalized cDNA pool prepared from 31 tissues produced 494 353 short transcript reads (STRs). Cluster analysis of these STRs, together with 10 817 Sanger ESTs, resulted in a pigeonpea trancriptome assembly (CcTA) comprising of 127 754 tentative unique sequences (TUSs). Functional analysis of these TUSs highlights several active pathways and processes in the sampled tissues. Comparison of the CcTA with the soybean genome showed similarity to 10 857 and 16 367 soybean gene models (depending on alignment methods). Additionally, Illumina 1G sequencing was performed on Fusarium wilt (FW)- and sterility mosaic disease (SMD)-challenged root tissues of 10 resistant and susceptible genotypes. More than 160 million sequence tags were used to identify FW- and SMD-responsive genes. Sequence analysis of CcTA and the Illumina tags identified a large new set of markers for use in genetics and breeding, including 8137 simple sequence repeats, 12 141 single-nucleotide polymorphisms and 5845 intron-spanning regions. Genomic resources developed in this study should be useful for basic and applied research, not only for pigeonpea improvement but also for other related, agronomically important legumes.

Biological Control of Late Leaf Spot of Peanut (Arachis hypogaea) with Chitinolytic Bacteria.

ABSTRACT Late leaf spot (LLS), caused by Phaeoisariopsis personata, is a foliar disease of groundnut or peanut (Arachis hypogaea) with high economic and global importance. Antifungal and chitinolytic Bacillus circulans GRS 243 and Serratia marcescens GPS 5, selected among a collection of 393 peanut-associated bacteria, were applied as a prophylactic foliar spray and tested for control of LLS. Chitin-supplemented application of B. circulans GRS 243 and S. marcescens GPS 5 resulted in improved biological control of LLS disease. Supplementation of bacterial cells with 1% (wt/vol) colloidal chitin reduced lesion frequency by 60% compared with application of bacterial cells alone, in the greenhouse. Chitinsupplemented application of GRS 243 and GPS 5 also resulted in improved and stable control of LLS in a repeated field experiment and increased the pod yields by 62 and 75%, respectively, compared with the control. Chitin-supplemented application of GPS 5 was tested in six onfarm trials, and the increase in pod yields was up to 48% in kharif (rainy season). A 55-kDa chitinase was purified from the cell-free culture filtrate of GPS 5 by affinity chromatography and gel filtration. Purified chitinase of S. marcescens GPS 5 (specific activity 120 units) inhibited the in vitro germination of P. personata conidia, lysed the conidia, and effectively controlled LLS in greenhouse tests, indicating the importance of chitinolysis in biological control of LLS disease by GPS 5.

International agricultural research tackling the effects of global and climate changes on plant diseases in the developing world

Climate change has a number of observed, anticipated, or possible consequences on crop health worldwide. Global change, on the other hand, incorporates a number of drivers of change, including global population increase, natural resource evolution, and supply–demand shifts in markets, from local to global. Global and climate changes interact in their effects on global ecosystems. Identifying and quantifying the impacts of global and climate changes on plant diseases is complex. A number of nonlinear relationships, such as the injury (epidemic)–damage (crop loss) relationship, are superimposed on the interplay among the three summits of the disease triangle (host, pathogen, environment). Work on a range of pathosystems involving rice, peanut, wheat, and coffee has shown the direct linkage and feedback between production situations and crop health. Global and climate changes influence the effects of system components on crop health. The combined effects of global and climate changes on diseases vary from one pathosystem to another within the tetrahedron framework (humans, pathogens, crops, environment) where human beings, from individual farmers to consumers to entire societies, interact with hosts, pathogens, and the environment. This article highlights international phytopathological research addressing the effects of global and climate changes on plant diseases in a range of crops and pathosystems.

Evaluation of Essential Oils and Their Components for Broad-Spectrum Antifungal Activity and Control of Late Leaf Spot and Crown Rot Diseases in Peanut

Clove oil, cinnamon oil, and five essential oil components (citral, eugenol, geraniol, limonene, and linalool) were tested for growth inhibition of 14 phytopathogenic fungi. Citral completely inhibited the growth of Alternaria alternata, Aspergillus flavus, Curvularia lunata, Fusarium moniliforme, F. pallidoroseum, and Phoma sorghina in paper disc agar diffusion assays. Cinnamon oil, citral, and clove oil as low as 0.01% (vol/vol) inhibited the spore germination of Cercospora arachidicola, Phaeoisariopsis personata, and Puccinia arachidis by >90% in vitro. Limonene and linalool were observed to be the least antifungal against the test fungi and were not used in further studies. Clove oil (1% vol/vol) applied as a foliar spray 10 min before Phaeoisariopsis personata inoculation reduced the severity of late leaf spot of peanut up to 58% when challenge inoculated with 104 conidia ml-1. This treatment was more effective (P = 0.01) than 0.5% (vol/vol) citral, cinnamon oil, or clove oil and 1% (vol/vol) eugenol or geraniol. Seed treatment with the test compounds had no effect on the incidence of crown rot in peanut in Aspergillus niger-infested soil. However, soil amendment with 0.25% (vol/wt) clove oil and cinnamon oil reduced the preemergence rotting by 71 and 67% and postemergence wilting by 58 and 55%, respectively, compared with the nontreated control. These two treatments were more effective (P < 0.01) than geraniol on preemergence rotting, and more effective than citral, eugenol, and geraniol on postemergence wilting. All treatments significantly outperformed the nontreated control but none were as effective as thiram treatment.

Advances in genetics and molecular breeding of three legume crops of semi-arid tropics using next-generation sequencing and high-throughput genotyping technologies.

Molecular markers are the most powerful genomic tools to increase the efficiency and precision of breeding practices for crop improvement. Progress in the development of genomic resources in the leading legume crops of the semi-arid tropics (SAT), namely, chickpea (Cicer arietinum), pigeonpea (Cajanus cajan) and groundnut (Arachis hypogaea), as compared to other crop species like cereals, has been very slow. With the advances in next-generation sequencing (NGS) and high-throughput (HTP) genotyping methods, there is a shift in development of genomic resources including molecular markers in these crops. For instance, 2,000 to 3,000 novel simple sequence repeats (SSR) markers have been developed each for chickpea, pigeonpea and groundnut. Based on Sanger, 454/FLX and Illumina transcript reads, transcriptome assemblies have been developed for chickpea (44,845 transcript assembly contigs, or TACs) and pigeonpea (21,434 TACs). Illumina sequencing of some parental genotypes of mapping populations has resulted in the development of 120 million reads for chickpea and 128.9 million reads for pigeonpea. Alignment of these Illumina reads with respective transcriptome assemblies have provided >10,000 SNPs each in chickpea and pigeonpea. A variety of SNP genotyping platforms including GoldenGate, VeraCode and Competitive Allele Specific PCR (KASPar) assays have been developed in chickpea and pigeonpea. By using above resources, the first-generation or comprehensive genetic maps have been developed in the three legume species mentioned above. Analysis of phenotyping data together with genotyping data has provided candidate markers for drought-tolerance-related root traits in chickpea, resistance to foliar diseases in groundnut and sterility mosaic disease (SMD) and fertility restoration in pigeonpea. Together with these trait-associated markers along with those already available, molecular breeding programmes have been initiated for enhancing drought tolerance, resistance to fusarium wilt and ascochyta blight in chickpea and resistance to foliar diseases in groundnut. These trait-associated robust markers along with other genomic resources including genetic maps and genomic resources will certainly accelerate crop improvement programmes in the SAT legumes.

Development of screening methods and identification of stable resistance to anthracnose in sorghum

Effective greenhouse- and field-screening techniques were developed to identify resistance to anthracnose (Colletotrichum graminicola) in grain sorghum (Sorghum bicolor). In greenhouse screening, sorghum plants were spray-inoculated at the 6–8 leaf stage with a conidial suspension (4 × 105 conidial ml−1) of C. graminicola. Inoculated plants were incubated in a high humidity chamber (⩾ 90% RH) for 24 h at 25–28°C and relocated to a greenhouse at 25 ± 2°C. Anthracnose development was scored 7–8 days after inoculation. In the field-screening technique, in every fifth row, a highly anthracnose-susceptible sorghum line was sown as an infector row. Ten days later, test lines were sown between infector row plants were inoculated at the 6–8 leaf stage with either spore suspension or by dropping infected sorghum grains into the leaf whorl. High humidity was provided by frequent overhead sprinkler or furrow irrigation. Test lines were scored for anthracnose development at the hard-dough stage. Significant positive correlation (r = 0.88, P < 0.001) was found for anthracnose severity between seedling screening in greenhouse and adult plant screening in the field. The field-screening technique was successfully transferred to several locations in Africa and India. Thirty lines were selected from more than 13 000 sorghum germplasm accessions and advanced breeding lines screened for anthracnose resistance, using the field-screening technique at Pantnagar (North India) between 1982 and 1991. They were evaluated in multilocational tests at hot spots in Burkina Faso, India, Nigeria, Zambia, and Zimbabwe for 1–10 years. Eleven lines (A 2267-2, IS 3547, IS 8283, IS 9146, IS 9249, IS 18758, SPV 386, PB 8892-2, PS 18601-3, PM 20873-1, and M 35610) showed stable resistance across these locations over the years. Some of the resistant lines are being converted into male-sterile lines through backcrossing with different sources of cytoplasmic male sterility.

Identification of Sources of Multiple Disease Resistance in Mini-core Collection of Chickpea

Host plant resistance is the major component in the management of fungal diseases in chickpea (Cicer arietinum). We screened a chickpea mini-core collection composed of 211 germ plasm accessions representing the diversity of the global chickpea germ plasm collection of 16,991, maintained at the International Crops Research Institute for the Semi-Arid Tropics to identify sources of multiple disease resistance. The accessions were screened for resistance against As-cochyta blight (Ascochyta rabiei), Botrytis gray mold (Botrytis cinerea), Fusarium wilt (Fusarium oxysporum f. sp. ciceris), and dry root rot (Rhizoctonia bataticola) under a controlled environment. High levels of resistance were observed to Fusarium wilt (FW), where 21 accessions were asymptomatic and 25 resistant. In all, 3, 55, and 6 accessions were moderately resistant to Ascochyta blight (AB), Botrytis gray mold (BGM), and dry root rot (DRR) respectively. ICC 11284 was the only accession moderately resistant to both AB and BGM. Combined resistance also was identified for DRR and FW in 4 accessions, and for BGM and FW in 11 accessions. Through this study, chickpea germ plasm accessions were identified that possess high levels of resistance to more than one fungal disease and would be useful in chickpea multiple disease resistance breeding programs.