Achievements of agricultural biotechnology: An initiative to double the farmer’s income through cutting edge technology

The population of the world is increasing nearly exponentially over time. To feed this population following the environment conservation protocol, it is essential to enhance the agricultural productivity even in the synchronizing agrarian land use pattern. To enhance the quality and productivity in agriculture sector, introducing the cutting edge technology is need of the hour.From ancient times, traditional approaches like selective breeding, adoption of agronomic management practices and application of indigenous technical knowledge have been used to attain resilience against various abiotic and biotic stresses. However, these traditional approaches are not sufficient to tackle the increasing repercussions of climate change and feed quality food to the expanding population. Therefore, in order to address these issues of climate change, population explosion and malnutrition, biotechnological interventions can be a promising approach. In the past, biotechnology based approaches have given successful products like Herbicide-resistant Soybean, Pusa Basmati 1, Bt Cotton, Bt Brinjal, Flavr-Savr tomato, a therapeutically significant product of Lithospermum erythrorhizon and Panax ginseng. Besides that many more need based products are in pipeline which is under scrutiny of regulatory bodies, policymakers and environmentalists. It is profoundly expected that in the coming day’s agricultural biotechnology applications will bring revolutionary changes to existing agricultural scenario. Therefore, in this review, we have summarized the achievement of agricultural biotechnology that is assisting to enhance the agricultural produce to double the income of farmers. However, this much is not enough; hence full utilization of all the sustainable agricultural biotechnological tools must come into the existence that definitely will boost the agricultural productivity

Physiological and Molecular Plant Pathology

Not AvailableQuantitative detection of pathogen DNA load is a crucial aspect in development of disease management strategies and breeding programs. In recent years, there have been several reports where formae speciales specific intergenic spacer (IGS) sequence based markers have been used for quantification of pathogen DNA in different plant and soil samples, through quantitative real-time PCR (qPCR). In the present study, we have utilized an IGS based marker, ISR 52, to detect and quantify Fusarium oxysporum f.sp. ciceris (Foc) DNA, using both conventional PCR and qPCR, in chickpea genotypes which contrast for resistance to Fusarium wilt. Our study reveals that the Foc DNA load was found to be significantly higher in the early wilting genotypes as compared to the wilt resistant genotypes. Late wilting genotype showed a spike in pathogen DNA load in later stage of plant growth. Phenotypic observation of disease progression in combination with qPCR data validated that the pathogen undergoes incubation period before manifestation of symptoms. The above observations provide evidence about the differential dynamics of pathogen build up inside different hosts during different time periods and probable reason for the earliness, lateness and resistance in wilting like traits in these genotype

Quantitative detection of pathogen load of Fusarium oxysporum f.sp. ciceris infected wilt resistant and susceptible genotypes of chickpea using intergenic spacer region-based marker

Highlights • Intergenic spacer based markers are robust molecular markers for detection of phytopathogenic fungi. • qPCR can be utilized as a molecular diagnostic tool to quantify pathogen DNA load at pictogram (pg) level. • Differential dynamics of pathogen DNA in chickpea genotypes contrasting for Fusarium wilt resistance was observed.Quantitative detection of pathogen DNA load is a crucial aspect in development of disease management strategies and breeding programs. In recent years, there have been several reports where formae speciales specific intergenic spacer (IGS) sequence based markers have been used for quantification of pathogen DNA in different plant and soil samples, through quantitative real-time PCR (qPCR). In the present study, we have utilized an IGS based marker, ISR 52, to detect and quantify Fusarium oxysporum f.sp. ciceris (Foc) DNA, using both conventional PCR and qPCR, in chickpea genotypes which contrast for resistance to Fusarium wilt. Our study reveals that the Foc DNA load was found to be significantly higher in the early wilting genotypes as compared to the wilt resistant genotypes. Late wilting genotype showed a spike in pathogen DNA load in later stage of plant growth. Phenotypic observation of disease progression in combination with qPCR data validated that the pathogen undergoes incubation period before manifestation of symptoms. The above observations provide evidence about the differential dynamics of pathogen build up inside different hosts during different time periods and probable reason for the earliness, lateness and resistance in wilting like traits in these genotypes